IndraLab

Statements


USP43 affects MYC
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USP43 binds MYC.
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sparser
"To test whether c-Myc directly binds to the USP43 promoter, we performed chromatin immunoprecipitation (ChIP) and qPCR."

sparser
"Collectively, these data suggest that c-Myc can directly bind to the promoter region of USP43 and activate USP43 transcription, confirming that c-Myc is a transcription factor for USP43."

sparser
"Coimmunoprecipitation assays indicated that several c-Myc mutants could interact with USP43, similar to wild-type c-Myc (Supplementary Fig. xref )."

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"Next, we performed a coimmunoprecipitation assay to investigate the potential interaction between USP43 and c-Myc."

sparser
"Additionally, the interaction between USP43 and c-Myc reduces the proximity of FBXW7 to c-Myc, indirectly stabilizing it."

sparser
"As shown in Fig. xref , USP43 interacted with the N-, N1-, N2-, and C1-terminus of c-Myc, while c-Myc interacted with both the N-terminus and the C-terminus of USP43."

sparser
"Moreover, endogenous USP43 interacted with c-Myc in T24 and 5637 cells (Fig. xref and Supplementary Fig. xref )."

sparser
"These findings indicate the interaction between USP43 and c-Myc."

sparser
"However, the efficacy of drugs targeting USP43 will be dependent on their ability to inhibit the deubiquitinase activity of USP43 and degrade USP43 protein or disrupt USP43-cMyc interaction."

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"Additionally, the interaction between USP43 and c-Myc reduces the proximity of FBXW7 to c-Myc, indirectly stabilizing it."
USP43 deubiquitinates MYC.
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USP43 deubiquitinates MYC. 3 / 3
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"These results suggest that wild-type USP43 primarily stabilizes c-Myc by directly deubiquitinating c-Myc, while USP43 with a loss of catalytic activity still protects c-Myc to some extent by competitively binding to c-Myc with FBXW7."

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"Next, the type of polyubiquitin chain of c-Myc deubiquitinated by USP43 was examined, and our data indicated that USP43 catalyzed the deubiquitination of the K48 chain but not the K63 chain of c-Myc, which is associated with proteasomal pathway degradation [28] (Fig. 5H)."

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"Further deubiquitination assays showed that USP43 was able to deubiquitinate wild-type c-Myc but not the c-Myc mutants K148R, K289R, and K148/289R (Fig. 5J)."
USP43 deubiquitinates MYC-K148R. 1 / 1
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"Further deubiquitination assays showed that USP43 was able to deubiquitinate wild-type c-Myc but not the c-Myc mutants K148R, K289R, and K148/289R (Fig. 5J)."
USP43 deubiquitinates MYC-K289R. 1 / 1
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"Further deubiquitination assays showed that USP43 was able to deubiquitinate wild-type c-Myc but not the c-Myc mutants K148R, K289R, and K148/289R (Fig. 5J)."
USP43 activates MYC.
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USP43 activates MYC. 5 / 5
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"This study reveals that USP43 promotes aerobic glycolysis and metastasis in BLCA by stabilizing c-Myc, thus providing a novel target for indirect inhibition of c-Myc."

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"To identify the lysine residue of c-Myc catalyzed by USP43, we constructed a series of c-Myc point mutant plasmids with lysine mutated to arginine."

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"We then constructed a double mutant of c-Myc and confirmed that K148 and K289 are indeed essential for USP43 catalysis of c-Myc (Fig. 5I and Supplementary Fig. S6F)."

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"USP43 antagonizes c-Myc degradation by FBXW7."

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"This partially explains the upregulation of USP43 in BLCA tissues, wherein amplified c-Myc increases USP43 mRNA levels."
USP43 increases the amount of MYC.
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USP43 increases the amount of MYC. 2 / 2
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"However, knockdown of USP43 decreased the c-Myc protein level in T24 and 5637 cells (Fig. 2C), while overexpression of USP43 increased the c-Myc protein level in T24, 5637, and UM-UC-3 cells (Fig. 2D)."

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"Additionally, c-Myc protein levels were increased by USP43 in a dose-dependent manner (Fig. 3B)."
USP43 affects ZEB1
2 1 | 16 6
USP43 binds ZEB1.
2 | 3 6
2 | 3 6

No evidence text available

No evidence text available

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"USP43 directly interacts with and deubiquitinates ZEB1, thus affecting the cell migration and EMT of CRC [88]."

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"Further investigation revealed a direct interaction between USP43 and ZEB1 in colorectal cell lines, wherein USP43 downregulates ZEB1 protein expression independent of its transcriptional regulation, thereby modulating the abundance of ZEB1 protein."

reach
"ZEB1 can directly interact with USP43 in cellular."

sparser
"Moreover, we have examined the potential interaction between USP43 protein and ZEB1 protein in cellular."

sparser
"In this study, Co-immunoprecipitation (Co-IP) was employed to study the potential interaction between USP43 protein and ZEB1 protein."

sparser
"Figure xref F showed that USP43 protein could interact with ZEB1 protein."

sparser
"Figure xref F and xref G had further identified the interaction between USP43 protein and ZEB1 protein."

sparser
"ZEB1 can directly interact with USP43 in cellular."
USP43 deubiquitinates ZEB1.
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USP43 deubiquitinates ZEB1. 7 / 7
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"USP43 can enhance CRC cell growth by inducing the deubiquitination of Zinc finger E-box-binding homeobox 1 (ZEB1) protein, which is closely associated with tumor cell proliferation, invasion, migration and expression of EMT-related biomarkers."

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"USP43 promoted cell proliferation, migration and invasion of colorectal cancer, and reduce the sensitivity of chemotherapy through deubiquitinating ZEB1 [12]."

"Meanwhile, <span class="match term0">USP43</span> can deubiquitinate and stabilize the <span class="match term1">ZEB1</span> protein, which plays an important role in the function of colorectal cancer."

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"In patients with osteosarcoma and lung metastasis, USP43 deubiquitinates ZEB1 and maintains its transcription [65], resulting in increased invasion of osteosarcoma cells via inducing EMT [88, 89]."

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"Meanwhile, USP43 can deubiquitinate and stabilize the ZEB1 protein, which plays an important role in the function of colorectal cancer."

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"USP43 could promote cell proliferation, invasion, and migration in colorectal cancer by regulating ZEB1 ubiquitylation degradation."

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"USP43 directly interacts with and deubiquitinates ZEB1, thus affecting the cell migration and EMT of CRC [88]."
USP43 activates ZEB1.
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USP43 activates ZEB1. 5 / 5
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"The results suggested that USP43 knockdown treated SW480 cells could significantly promote the degradation of the remaining ZEB1 protein in cells compared to that normal SW480 cells (P < 0.01)."

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"Meanwhile, USP43 overexpression treated DLD1 cells could significantly decrease the degradation of the remaining ZEB1 protein in cells compared to that normal DLD1 cells (P < 0.01)."

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"Figure XREF_FIG K and 5L suggested that USP43 overexpression in DLD1 cells could significantly promote the remaining ZEB1 protein in cells compared to that normal DLD1 cells (P < 0.01)."

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"Meanwhile, USP43 knockdown treated SW480 cells could significantly decrease the remaining ZEB1 protein in cells compared to that normal SW480 cells (P < 0.01)."

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"USP43 directly regulates ZEB1 protein, mediating proliferation and metastasis of colorectal cancer."
USP43 decreases the amount of ZEB1.
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USP43 decreases the amount of ZEB1. 2 / 2
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"Further investigation revealed a direct interaction between USP43 and ZEB1 in colorectal cell lines, wherein USP43 downregulates ZEB1 protein expression independent of its transcriptional regulation, thereby modulating the abundance of ZEB1 protein."

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"Moreover, USP43 can reduce ZEB1 protein expression without affecting its transcription."
MYC affects USP43
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MYC binds USP43.
| 5 12
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sparser
"To test whether c-Myc directly binds to the USP43 promoter, we performed chromatin immunoprecipitation (ChIP) and qPCR."

sparser
"Collectively, these data suggest that c-Myc can directly bind to the promoter region of USP43 and activate USP43 transcription, confirming that c-Myc is a transcription factor for USP43."

sparser
"Coimmunoprecipitation assays indicated that several c-Myc mutants could interact with USP43, similar to wild-type c-Myc (Supplementary Fig. xref )."

reach
"Next, we performed a coimmunoprecipitation assay to investigate the potential interaction between USP43 and c-Myc."

sparser
"Additionally, the interaction between USP43 and c-Myc reduces the proximity of FBXW7 to c-Myc, indirectly stabilizing it."

sparser
"As shown in Fig. xref , USP43 interacted with the N-, N1-, N2-, and C1-terminus of c-Myc, while c-Myc interacted with both the N-terminus and the C-terminus of USP43."

sparser
"Moreover, endogenous USP43 interacted with c-Myc in T24 and 5637 cells (Fig. xref and Supplementary Fig. xref )."

sparser
"These findings indicate the interaction between USP43 and c-Myc."

sparser
"However, the efficacy of drugs targeting USP43 will be dependent on their ability to inhibit the deubiquitinase activity of USP43 and degrade USP43 protein or disrupt USP43-cMyc interaction."

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"Additionally, the interaction between USP43 and c-Myc reduces the proximity of FBXW7 to c-Myc, indirectly stabilizing it."
MYC increases the amount of USP43.
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MYC increases the amount of USP43. 3 / 3
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"Stable c-Myc can function as a transcription factor to activate USP43 transcription."

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"C-Myc oncoprotein promotes the transcription of USP43 and regulates the transcription of at least 15% of the entire genome as a transcription factor."

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"Moreover, in 293 T cells, exogenous expression of c-Myc increased the mRNA level of USP43 (Fig. 7F)."
MYC activates USP43.
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MYC activates USP43. 3 / 3
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"The dual-luciferase reporter assay revealed that exogenous c-Myc significantly increased the activity of the USP43 promoter."

sparser
"Furthermore, MYC transcriptionally activates POLD1 and USP43, forming reciprocal positive feedback loops (POLD1-MYC and USP43-MYC) that promote BLCA progression [ xref , xref ]."

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"Furthermore, MYC transcriptionally activates POLD1 and USP43, forming reciprocal positive feedback loops (POLD1-MYC and USP43-MYC) that promote BLCA progression [42, 43]."

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"For instance, USP43 promoted cell proliferation, migration and invasion of colorectal cancer [12]."

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"USP43 could promote the proliferation, migration, and invasion of colorectal cancer."

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"USP43 promotes proliferation of colorectal cancer cells in vitro."

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"For cell proliferation analysis, USP43 knockdown in SW480 cells could significantly reduce cell proliferation compared with those in normal SW480 cells on days 2, 3, 4, 5 (P < 0.01)."

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"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."

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"USP43 overexpression promoted EOC cell proliferation, enhanced the ability of migration and invasion, decreased cisplatin sensitivity and inhibited apoptosis."

eidos
"USP43 could promote cell proliferation , invasion , and migration in colorectal cancer by regulating ZEB1 ubiquitylation degradation ."

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"USP43 promoted cell proliferation, migration, invasion and chemoresistance of EOC."

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"Overexpression of USP43 significantly increased cell proliferation (Fig. 3D and F)."

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"USP43 overexpression promoted PANC-1 cell proliferation (P = 0.0018), but USP43 knockdown decreased PANC02 cell proliferation (P < 0.001)."

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"Conversely, USP43 overexpression consistently exhibits the opposite effect and represses cell proliferation and tumor growth, providing further support for a tumor suppressive role of USP43 in breast [MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP43 affects NPPA
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sparser
"USP monograph (USP43NF38) also touched upon the process of enrichment of deamidated variant >5% by acidic treatment."

sparser
"The criteria of benzoin from Chinese pharmacopoeia (ChP 2020), USA pharmacopoeia (USP43-NF38), European pharmacopoeia (EP10.0), Japanese pharmacopoeia (JP18) and Indian pharmacopoeia (IP2018) are summarized in xref , in which content determination, ethanol-insoluble matter, acid-insoluble ash, loss on drying, total ash and presence of dammar gum require detailed analysis [ xref , xref , xref , xref , xref ]."

sparser
"At present, there is no quality control for the polymerized impurities in United States Pharmacopoeia (USP43-NF38) [7] containing mezlocillin sodium, and Japanese Pharmacopoeia (JP17) [8] and Korean P[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

sparser
"Monographs of all three natural CDs and two of their derivatives can be found in the United States Pharmacopoeia- National Formulary (USP43NF38) and the European Pharmacopoeia (Pharmacopoeia Europaea[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

sparser
"In addition, the limit of the number of micro-particles ≥10 and 25 μm in 100-mL filling-volume injections is consistent with those indicated in the pharmacopoeias of all countries, such as USP43NF38, European Pharmacopoeia 10.0 and Chinese Pharmacopoeia 2020, with limits set as ≤12 and 2 particles/mL."

sparser
"A standard of upper loss on drying value of 7% is stated in the USP monograph (USP43-NF38)."

sparser
"USP43-NF38, VP5, and KP12 provided small numbers of stipulations for mineral medicines."

sparser
"Three syrup bases were used: a sugar-free vehicle for oral solution (according to USP43-NF38), a vehicle with glucose and hydroxypropyl cellulose (according to the DAC/NRF2018) and a commercially available SyrSpend Alka base."

sparser
"BP6, IP2018, Korean Pharmacopoeia 12th edition (KP12) and United States Pharmacopoeia and National Formulary 2020 (USP43-NF38) provided stipulations of impurities for most of the animal/botanical medicines (95%, 80%, 95%, and 69%, respectively)."

sparser
"In The United States Pharmacopeia (USP43-NF38) [United States Pharmacopeia Convention, Inc.: Rockville, MD, USA, 2023], the drug is more soluble, and in fact all of the samples can release the dose of the drug within an hour."
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"USP43 potentially regulates cancer invasion by modulating EMT-associated transcription factors, such as ZEB1 or SNAIL, in breast cancer, colorectal cancer, and osteosarcoma."

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"In breast cancer, USP43 promotes invasion and metastasis through invadopodia formation."

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"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."

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"USP43 knockdown in SW480 cells could significantly inhibit cell migration and invasion compared to that in the normal SW480 cells (P < 0.01)."

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"However, USP43 overexpression in DLD1 cells could promote cell migration and invasion compared to that in the normal DLD1 cells (P < 0.01)."

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"For instance, USP43 promoted cell proliferation, migration and invasion of colorectal cancer [12]."

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"Meanwhile, ZEB1overexpression could effectively reverse the changes in invasion caused by USP43 overexpression in SW480 cells (P < 0.01)."

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"USP43 overexpression promoted EOC cell proliferation, enhanced the ability of migration and invasion, decreased cisplatin sensitivity and inhibited apoptosis."

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"Furthermore, USP43 was highly expressed in colorectal cancer (CRC) and increased CRC cell proliferation, invasion, and migration [23]."

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"The study delves into the tumor-promoting impact in EOC, showing that USP43 enhances the proliferation, invasion, and migration of EOC, and facilitates EOC cells to enter the cell cycle’s proliferation phase.Cisplatin is a primary chemotherapeutic treatment for EOC."

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"For instance, USP43 modulates the infiltration of immune cells surrounding pancreatic ductal adenocarcinoma, thereby affecting patient prognosis [7]."
USP43 bound to NuRD inhibits Neoplasm Invasiveness. 1 / 1
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"Therefore, it has been established that the USP43/NuRD complex inhibits the growth, invasion, and metastasis of breast cancer cells; thus, USP43 may serve as a suppressor of breast cancer."
USP43 affects cisplatin
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USP43 inhibits cisplatin.
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"Taken together, our results suggested that USP43 impaired the sensitivity of EOC cells to cisplatin by activating the Wnt/β-catenin signaling pathway through HDAC2."

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"Notably, knockdown of USP43 enhanced cisplatin-induced apoptosis (Fig. 6C), while USP43 overexpression diminished the effect of cisplatin (Fig. 6D)."

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"In EOC, USP43 promotes the proliferation and impairs cisplatin sensitivity."

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"In the current study, we demonstrated that USP43 facilitated the malignant behaviors, and decreased the sensitivity of cisplatin to EOC cells."

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"These data suggested that USP43 reduced cisplatin sensitivity in EOC cells through suppressing DNA damage."

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"USP43 impairs cisplatin sensitivity in epithelial ovarian cancer through HDAC2-dependent regulation of Wnt/beta-catenin signaling pathway."

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"USP43 overexpression promoted EOC cell proliferation, enhanced the ability of migration and invasion, decreased cisplatin sensitivity and inhibited apoptosis."

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"To confirm whether HDAC2 is involved in the USP43-induced reduction of cisplatin sensitivity in EOC cells, USP43 over-expressed cells were transfected with si-HDAC2 or si-NC."

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"The overexpression of USP43 attenuated the inhibition of cisplatin on EOC cells, while HDAC2 silencing reversed the result (Fig. 10C)."

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"USP43 promotes the proliferation of epithelial ovarian cancer (EOC) and impairs its cisplatin sensitivity."
USP43 activates cisplatin.
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"These results showed that USP43 promoted the sensitivity of EOC cells to cisplatin via HDAC2."
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"This study reveals that USP43 promotes aerobic glycolysis and metastasis in BLCA by stabilizing c-Myc, thus providing a novel target for indirect inhibition of c-Myc."

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"In addition, studies have shown that USP43 mediates metastasis in breast and colon cancer [12, 59], but it has not been reported in ovarian cancer metastasis or recurrence, and it will be a direction for our investigation in the future.In conclusion, USP43 impaired cisplatin sensitivity by activating the Wnt/β-catenin signaling pathway via HDAC2 deubiquitylation, thereby promoting EOC progression."

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"In breast cancer, USP43 promotes invasion and metastasis through invadopodia formation."

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"In BLCA, USP43 promotes glycolysis and metastasis."

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"In vivo, USP43 knockdown led to reduced tumor growth and lung metastasis."

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"Overall, these findings suggest that USP43 promotes BLCA cell metastasis."

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"USP43 promotes glycolysis and metastasis in bladder cancer (BLCA)."

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"Moreover, USP43 may stimulate the metastasis of BLCA."

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"To further investigate if USP43 mediated the function of Ca 2.2 in metastasis in vivo, we transplanted luciferase-tagged MDA-MB-436 cells stably expressing Ca 2.2 shRNA and USP43 cDNA constructs into mice."
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"We show that USP43 strongly suppresses the growth and metastasis of breast cancer in vivo."

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"Meanwhile, previous study indicated that USP43 could remarkably inhibit the growth and metastasis of breast cancer though affecting EGFR/PI3K/AKT XREF_BIBR."
USP43 bound to NuRD inhibits Neoplasm Metastasis. 1 / 1
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"Therefore, it has been established that the USP43/NuRD complex inhibits the growth, invasion, and metastasis of breast cancer cells; thus, USP43 may serve as a suppressor of breast cancer."
ZEB1 affects USP43
2 | 3 6
2 | 3 6

No evidence text available

No evidence text available

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"USP43 directly interacts with and deubiquitinates ZEB1, thus affecting the cell migration and EMT of CRC [88]."

reach
"Further investigation revealed a direct interaction between USP43 and ZEB1 in colorectal cell lines, wherein USP43 downregulates ZEB1 protein expression independent of its transcriptional regulation, thereby modulating the abundance of ZEB1 protein."

reach
"ZEB1 can directly interact with USP43 in cellular."

sparser
"Moreover, we have examined the potential interaction between USP43 protein and ZEB1 protein in cellular."

sparser
"In this study, Co-immunoprecipitation (Co-IP) was employed to study the potential interaction between USP43 protein and ZEB1 protein."

sparser
"Figure xref F showed that USP43 protein could interact with ZEB1 protein."

sparser
"Figure xref F and xref G had further identified the interaction between USP43 protein and ZEB1 protein."

sparser
"ZEB1 can directly interact with USP43 in cellular."
P14_3_3 affects USP43
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sparser
"Moreover, the interaction between 14-3-3 and USP43 could be replicated using Culyculin A as a phosphatase inhibitor (Resjö et al, xref ), and conversely, prevented by Lambda PP (Fig.  xref )."

sparser
"We examined if the USP43 and 14-3-3 interaction was important for the recruitment of HIF-1α, and observed that USP43 loss decreased levels of HIF-1α associated with endogenous 14-3-3 (Fig.  xref )."

sparser
"However, the association of USP43 with 14-3-3 was important for regulating HIF-1 signalling, as pan-siRNA-mediated depletion of 14-3-3 (targeting 6 of 7 isoforms) (Fig.  xref ) reduced activation of the fluorescent HIF reporter and endogenous CA9, without affecting HIF-1α protein and mRNA levels (Figs.  xref and  xref )."

sparser
"Mechanistically, USP43 associates with 14-3-3 proteins in a hypoxia and phosphorylation dependent manner to increase the nuclear pool of HIF-1."

sparser
"It is, therefore, plausible that USP43 interacts with different 14-3-3 proteins depending on the context."

sparser
"In addition, as 14-3-3 proteins interact with phosphorylated ligands (Fu et al, xref ), phosphorylation is likely to provide the recruitment signal, in keeping with our observation that Ser phosphorylated USP43 bound 14-3-3 proteins."

sparser
"USP43 associates with 14-3-3 proteins to regulate HIF-1 signalling."

sparser
"We confirmed that USP43 binds 14-3-3 proteins, using overexpressed HA-USP43 and endogenous USP43 in HeLa cells (Fig.  xref ), consistent with the DUB mass spectrometry interactome (Sowa et al, xref )."

sparser
"Moreover, we found that 14-3-3 proteins bound USP43 more strongly in 1% oxygen (Fig.  xref )."

sparser
"The association of USP43 with 14-3-3 to facilitate a HIF-1-specific response provides a further layer of complexity in how HIF signalling is controlled and helps explain how differential transcription programmes are initiated."
USP43 is modified
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USP43 is phosphorylated.
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USP43 is phosphorylated. 2 / 2
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sparser
"Consistently, we showed that USP43 is phosphorylated using Lambda protein phosphatase (Lambda PP) and a gel shift assay (Fig.  xref )."

sparser
"In addition, as 14-3-3 proteins interact with phosphorylated ligands (Fu et al, xref ), phosphorylation is likely to provide the recruitment signal, in keeping with our observation that Ser phosphorylated USP43 bound 14-3-3 proteins."
USP43 is phosphorylated on S1041. 1 / 1
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No evidence text available
USP43 is phosphorylated on S851. 1 / 1
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No evidence text available
USP43 is phosphorylated on Y835. 1 / 1
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No evidence text available
USP43 is phosphorylated on S848. 1 / 1
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No evidence text available
USP43 is phosphorylated on S846. 1 / 1
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No evidence text available
USP43 is ubiquitinated.
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USP43 is ubiquitinated. 2 / 2
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sparser
"The proteins most affected by all three CGs were all significantly upregulated and included glycolytic enzyme GOT2, glutamate dehydrogenase GLUD1, hepatoma‐derived growth factor‐related protein HDGFL2, LIM and SH3 domain protein LASP1, cytochrome c CYCS, and de‐ubiquitinating enzyme USP43."

sparser
"Moreover, we have investigated the potential relationships between USP43 ubiquitination and ZEB1 in USP43 overexpression DLD1 cells."
USP43 is methylated.
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USP43 is methylated. 1 / 1
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sparser
"Based on these findings, the Disease Meth web tool () was used to analyze the difference of USP43 methylation level in OV and normal tissues."
USP43 affects HDAC2
2 | 6 1
USP43 binds HDAC2.
2 | 1 1
2 | 1 1

No evidence text available

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"The interaction between USP43 and HDAC2 was confirmed by Co-IP assay (Fig. 9C)."

sparser
"The interaction between USP43 and HDAC2 was confirmed by Co-IP assay (Fig.  xref C)."

No evidence text available
USP43 inhibits HDAC2.
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USP43 inhibits HDAC2. 2 / 2
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"Mechanistically, USP43 inhibited HDAC2 degradation and enhanced HDAC2 protein stability through its deubiquitylation function."

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"HDAC2 silencing elevated apoptosis rate induced by overexpression of USP43 (Fig. 10D)."
USP43 activates HDAC2.
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USP43 activates HDAC2. 2 / 2
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"Mechanistically, USP43 inhibited HDAC2 degradation and enhanced HDAC2 protein stability through its deubiquitylation function."

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"These results demonstrated that USP43 diminished HDAC2 degradation via deubiquitylation."
USP43 increases the amount of HDAC2.
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USP43 increases the amount of HDAC2. 1 / 1
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"With cycloheximide treatment, we observed that USP43 knockdown decreased the expression of HDAC2 in HEY cells, indicating that downregulation of USP43 reduced HDAC2 stability (Fig. 9D)."
USP43 affects CTTN
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USP43 increases the amount of CTTN.
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USP43 increases the amount of CTTN. 3 / 3
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"Conversely, over-expression of USP43 increased cortactin protein expression without affecting its expression at the transcriptional level (Fig. 5D, E)."

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"These results indicated that USP43 mediated the functions of Ca 2.2 in cortactin expression, invadopodia formation, ECM degradation, and metastasis."

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"We then transfected the cDNAs of these six DUBs into MDA-MB-231 cells, and immunoblotting showed that only USP43 increased cortactin expression (Supplementary Fig. 9A)."
USP43 decreases the amount of CTTN.
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USP43 decreases the amount of CTTN. 2 / 2
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"Knock-down of USP43 in MDA-MB-231 cells decreased the expression of cortactin at the protein level (Fig. 5B) but did not affect its transcript (Fig. 5C)."

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"The addition of MG132 successfully rescued the decrease of cortactin expression caused by USP43 knock-down (Fig. 5F), while the addition of CHX resulted in more unstable cortactin protein in USP43 knock-down cells (Fig. 5G)."
USP43 binds CTTN.
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sparser
"We first determined whether USP43 interacted with cortactin."

sparser
"Immunoprecipitation showed that USP43 interacted with cortactin in MDA-MB-231 cells (Fig. xref )."
USP43 ubiquitinates CTTN.
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USP43 leads to the ubiquitination of CTTN. 1 / 1
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"We next investigated whether USP43 was able to modulate cortactin ubiquitination in MDA-MB-231 cells."
USP43 activates CTTN.
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USP43 activates CTTN. 1 / 1
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"Together, these results suggested that USP43 directly regulates cortactin stability through deubiquitination."
NFATC1 affects USP43
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NFATC1 increases the amount of USP43.
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NFATC1 increases the amount of USP43. 3 / 3
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"We found that depletion of NFAT2 and NFAT3 could significantly reduced USP43 mRNA expression (Fig. 7D, Supplementary Fig. 11)."

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"These data suggested that NFAT2 directly regulates USP43 transcription."

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"(p29) N-type CaV2.2 promotes metastasis by modulating the activation of calcium-dependent phosphatase/nuclear factor of activated NFAT2 signaling pathways, which upregulates USP43 expression by dephos[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
Unphosphorylated NFATC1 increases the amount of USP43. 1 / 1
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"(p29) N-type CaV2.2 promotes metastasis by modulating the activation of calcium-dependent phosphatase/nuclear factor of activated NFAT2 signaling pathways, which upregulates USP43 expression by dephos[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
NFATC1 activates USP43.
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NFATC1 activates USP43. 4 / 4
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"To verify whether USP43 is directly regulated by NFAT2, we cloned USP43 promoter (−213~−1847bp) into pGL3-basic vector and performed dual luciferase reporter assay."

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"USP43 is directly regulated by NFAT2."

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"Expression of NFAT2 increased USP43 mRNA and protein expression (Fig. 7F, G)."

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"These data indicated that NFAT2 mediates the regulation of USP43 by Ca 2.2."
NFATC1 binds USP43.
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sparser
"We used Chromatin Immunoprecipitation (ChIP) analysis to further determined the direct interactions of NFAT2 with USP43 promoter in MDA-MB-231 cells, ChIP analysis indicated the significant enrichment of USP43 promoter as well as BMI1 promoter which is a well-established direct target gene of NFAT2 [ xref ] and served as a control in NFAT2 immunoprecipitation (Fig. xref , Supplementary Fig. xref )."
Calcium(2+) affects USP43
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Calcium(2+) increases the amount of USP43.
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Calcium(2+) increases the amount of USP43. 4 / 4
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"Ca v 2.2 by activating calcineurin/NFAT2 dephosphorylation modulates the deubiquinating enzyme USP43 expression that promotes invadopodia formation by stabilizing cortactin, which lead to metastasis.A[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"Interestingly, Ca v 2.2 upregulates USP43 expression through NFAT2 dephosphorylation and nuclear localization."

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"We then investigated the regulation of USP43 by Ca 2.2 and found that knock-down of Ca 2.2 decreased USP43 expression whereas over-expression of Ca 2.2 increased USP43 expression transcriptionally and at the protein level (Fig. 7A–C)."

reach
"NFAT2 knock-down abolished the up-regulation of USP43 levels by Ca 2.2 (Fig. 8A, B)."
Calcium(2+) activates USP43.
| 2
| 2

reach
"These data indicated that NFAT2 mediates the regulation of USP43 by Ca 2.2."

reach
"The involvement of USP43 in breast cancer has been documented in two previous studies suggesting that Ca 2.2 upregulates USP43 to promote tumorigenesis in breast cancer [36]."
Calcium(2+) decreases the amount of USP43.
| 1
Calcium(2+) decreases the amount of USP43. 1 / 1
| 1

reach
"We then investigated the regulation of USP43 by Ca 2.2 and found that knock-down of Ca 2.2 decreased USP43 expression whereas over-expression of Ca 2.2 increased USP43 expression transcriptionally and at the protein level (Fig. 7A–C)."
YWHAB affects USP43
6 |
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Bisphenol A affects USP43
5 |
Bisphenol A decreases the amount of USP43.
3 |
Bisphenol A decreases the amount of USP43. 3 / 3
3 |

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Bisphenol A methylates USP43.
1 |
1 |

No evidence text available
Bisphenol A demethylates USP43.
1 |
Bisphenol A demethylates USP43. 1 / 1
1 |

No evidence text available
YWHAE affects USP43
5 |
5 |

No evidence text available

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| 5

reach
"USP43 overexpression promoted EOC cell proliferation, enhanced the ability of migration and invasion, decreased cisplatin sensitivity and inhibited apoptosis."

reach
"HDAC2 silencing elevated apoptosis rate induced by overexpression of USP43 (Fig. 10D)."

reach
"Our results demonstrated that USP43 inhibition of apoptosis affected the sensitivity of EOC to cisplatin.High-level expression of HDAC2 promotes cancer progression through various signal pathways, including breast cancer [38, 39], non-small cell lung cancer [16], liver cancer [40]."

reach
"USP43 suppressed DNA damage and apoptosis, thereby reducing the sensitivity of EOC cells to cisplatin."

reach
"USP43 overexpression diminished cell apoptosis induced by cisplatin, and ICG-001 treatment restored this effect (Fig. 10L)."
USP43 affects YWHAE
5 |
5 |

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USP43 affects Wnt/β-catenin
| 5
USP43 activates Wnt/β-catenin.
| 4
USP43 activates Wnt/β-catenin. 4 / 4
| 4

reach
"Notably, knockdown of HDAC2 diminished the activation of Wnt/β-catenin signaling pathway caused by upregulation of USP43 (Fig. 10J, K)."

reach
"These results indicated that USP43 activated Wnt/β-catenin signaling pathway through HDAC2.To further determine whether USP43 regulates the sensitivity of EOC cells to cisplatin via the Wnt/β-catenin signaling pathway, EOC cells were co-treated with Wnt/β-catenin signaling pathway inhibitor ICG-001 and cisplatin."

reach
"Mechanically, USP43 activated the Wnt/β-catenin signaling pathway through inhibiting ubiquitin-mediated degradation of HDAC2 to induce EOC cell chemoresistance.USP43 functions as a tumor promoter in multiple cancers."

reach
"Further research found that USP43 induced activation of the Wnt/β-catenin signaling pathway by regulating HDAC2."
USP43 inhibits Wnt/β-catenin.
| 1
USP43 inhibits Wnt/β-catenin. 1 / 1
| 1

reach
"Taken together, our results suggested that USP43 impaired the sensitivity of EOC cells to cisplatin by activating the Wnt/β-catenin signaling pathway through HDAC2."
USP43 affects Neoplasms
| 5
USP43 activates Neoplasms.
| 4
| 4

reach
"In vivo xenograft tumors, silencing USP43 slowed tumor growth and enhanced cisplatin sensitivity."

reach
"Knockdown of USP43 inhibited tumor growth and enhanced cisplatin sensitivity of EOCin vivo.."

reach
"Thus, we concluded that knockdown of USP43 inhibited tumor growth and enhanced cisplatin sensitivity of EOC in vivo."

reach
"These findings suggest that the two functions of USP43 operate in coordination to maintain c-Myc as an oncoprotein and promote tumor progression (Fig. 8)."
USP43 inhibits Neoplasms.
| 1
| 1

reach
"Conversely, USP43 overexpression consistently exhibits the opposite effect and represses cell proliferation and tumor growth, providing further support for a tumor suppressive role of USP43 in breast [MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP43 affects HIF1A
| 5
| 5

sparser
"Importantly, the interaction between HIF-1α and USP43 did not prevent the formation of a HIF heterodimer, as HIF1-α and HIF1β still associated in USP43 null HeLa cells (Fig.  xref ), and neither USP43 depletion nor overexpression altered HIF-1α degradation kinetics using cycloheximide chase assay of HIF-1α degradation (Fig.  xref )."

sparser
"Instead, we show that USP43 associates with HIF-1α and promotes the nuclear accumulation of HIF-1 and the chromatin binding of the transcriptional complex to specific HIF-1 target genes."

sparser
"To understand how USP43 may facilitate a HIF-1 transcriptional response, we examined if USP43 associated with HIF-1α in hypoxia by incubating HeLa cells in 21 or 1% oxygen for 6 h and immunoprecipitating endogenous USP43 or HIF-1α."

sparser
"USP43 bound to HIF-1α in hypoxia, and depletion of HIF1β did not prevent the association between endogenous USP43 and HIF-1α (Figs.  xref and  xref )."

sparser
"The association of USP43 with HIF-1α was also observed in other cell lines (A549 and MCF7 cells) (Fig.  xref )."
4 |
Valproic acid increases the amount of USP43. 4 / 4
4 |

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| 3

reach
"These results indicated that USP43 activated Wnt/β-catenin signaling pathway through HDAC2.To further determine whether USP43 regulates the sensitivity of EOC cells to cisplatin via the Wnt/β-catenin signaling pathway, EOC cells were co-treated with Wnt/β-catenin signaling pathway inhibitor ICG-001 and cisplatin."

reach
"Notably, knockdown of HDAC2 diminished the activation of Wnt/β-catenin signaling pathway caused by upregulation of USP43 (Fig. 10J, K)."

reach
"Mechanically, USP43 activated the Wnt/β-catenin signaling pathway through inhibiting ubiquitin-mediated degradation of HDAC2 to induce EOC cell chemoresistance.USP43 functions as a tumor promoter in multiple cancers."
| 1

reach
"Taken together, our results suggested that USP43 impaired the sensitivity of EOC cells to cisplatin by activating the Wnt/β-catenin signaling pathway through HDAC2."

reach
"In BLCA, USP43 promotes glycolysis and metastasis."

reach
"This study reveals that USP43 promotes aerobic glycolysis and metastasis in BLCA by stabilizing c-Myc, thus providing a novel target for indirect inhibition of c-Myc."

reach
"USP43 promotes glycolysis and metastasis in bladder cancer (BLCA)."

reach
"These results demonstrate that USP43 positively regulates glycolysis in BLCA and c-Myc transcriptional activity."

reach
"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."

reach
"Silencing of USP43 reduced cell proliferation, migration, invasion, and the epithelial-mesenchymal transition (EMT) process."

reach
"In addition, USP43 could promote tumorigenesis by regulating cell cycle and EMT process in breast cancer XREF_BIBR."

reach
"We next detected whether USP43 regulated EMT, our results demonstrated that USP43 promoted EMT through regulated snail, thereby facilitated breast cancer cells metastasis."
USP43 affects VIM
| 4
USP43 increases the amount of VIM. 2 / 2
| 2

reach
"Meanwhile, USP43 knockdown in SW480 cells could inhibit and promote the protein expressions of N-cadherin and Vimentin and protein expressions of N-cadherin, respectively."

reach
"USP43 knockdown in SW480 cells could effectively inhibit protein expressions of N-cadherin and Vimentin (P < 0.01)."
Modified USP43 increases the amount of VIM. 2 / 2
| 2

reach
"Therefore, USP43 overexpression in DLD1 cells could promote and inhibit the protein expressions of N-cadherin and Vimentin and protein expressions of N-cadherin, respectively."

reach
"Moreover, USP43 overexpression in DLD1 cells could effectively increase protein expressions of N-cadherin and Vimentin (P < 0.01)."
USP43 affects TAFAZZIN
| 3 1
USP43 binds TAFAZZIN.
| 2 1
| 2 1

sparser
"Immunofluorescence staining and co-immunoprecipitation (Co-IP) assays were used to explore the interaction between USP43 and TAZ."

reach
"Immunofluorescence staining and co-immunoprecipitation (Co-IP) assays were used to explore the interaction between USP43 and TAZ."

reach
"Co-IP and ubiquitination assays revealed that USP43 interacted with and stabilized TAZ by inhibiting TAZ ubiquitination."
USP43 activates TAFAZZIN.
| 1
| 1

reach
"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."
USP43 affects NuRD
| 4
USP43 binds NuRD. 4 / 4
| 4

reach
"The USP43/NuRD complex inhibits the activity of EGFR and AKT, while the EGFR/PI3K/AKT signaling pathway regulates the behavior of USP43."

reach
"Therefore, it has been established that the USP43/NuRD complex inhibits the growth, invasion, and metastasis of breast cancer cells; thus, USP43 may serve as a suppressor of breast cancer."

reach
"Histone H2BK120 can be deubiquitinated by the complex of USP43 and NuRD complex and be reactivated."

reach
"It has been discovered that the USP43/NuRD complex inhibits the expression of numerous cancer-related genes, including the epidermal growth factor receptor (EGFR)."
USP43 affects MTA3
4 |
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USP43 affects FBXW7
| 4
USP43 inhibits FBXW7.
| 3
USP43 inhibits FBXW7. 2 / 2
| 2

reach
"Given that both USP43 and FBXW7 bind to the MBI of c-Myc, it seems reasonable to assume that increased USP43 may impede FBXW7’s access to c-Myc."

reach
"Overall, our results indicate that USP43 antagonizes the FBXW7-mediated degradation of c-Myc and cooperates with FBXW7 to regulate the migration ability of BLCA cells."
USP43 bound to MYC inhibits FBXW7. 1 / 1
| 1

reach
"Additionally, the interaction between USP43 and c-Myc reduces the proximity of FBXW7 to c-Myc, indirectly stabilizing it."
USP43 binds FBXW7.
| 1
| 1

reach
"In BLCA, DNA polymerase POLD1 and the ubiquitin-specific protease USP43 competitively bind to MYC, preventing its interaction with FBXW7 and thereby stabilizing MYC protein levels."
USP43 affects EOC
| 4
USP43 activates EOC.
| 3
USP43 activates EOC. 3 / 3
| 3

reach
"In EOC, USP43 promotes the proliferation and impairs cisplatin sensitivity."

reach
"The study delves into the tumor-promoting impact in EOC, showing that USP43 enhances the proliferation, invasion, and migration of EOC, and facilitates EOC cells to enter the cell cycle’s proliferation phase.Cisplatin is a primary chemotherapeutic treatment for EOC."

reach
"USP43 promoted cell proliferation, migration, invasion and chemoresistance of EOC."
USP43 inhibits EOC.
| 1
USP43 inhibits EOC. 1 / 1
| 1

reach
"Our results indicated that USP43 reduced the sensitivity of EOC to cisplatin by decreasing apoptosis."
USP43 affects EGFR
| 4
USP43 inhibits EGFR.
| 2
USP43 bound to NuRD inhibits EGFR. 2 / 2
| 2

reach
"The USP43/NuRD complex inhibits the activity of EGFR and AKT, while the EGFR/PI3K/AKT signaling pathway regulates the behavior of USP43."

reach
"It has been discovered that the USP43/NuRD complex inhibits the expression of numerous cancer-related genes, including the epidermal growth factor receptor (EGFR)."
USP43 increases the amount of EGFR.
| 1
USP43 increases the amount of EGFR. 1 / 1
| 1

reach
"For example, as USP43 downregulation may promote breast cancer pathogenesis by altering H2Bub1-mediated regulation of EGFR expression (Section 5.1 ), an epigenome editing tool that selectively rescues[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP43 activates EGFR.
| 1
USP43 activates EGFR. 1 / 1
| 1

reach
"Ubiquitin-specific peptidase 43 initiates the progression of breast cancer by interacting with the nucleosome remodeling and deacetylase (NuRD) complex , catalyzing H2BK120 deubiquitylation, and subse[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP43 affects CDH2
| 4
Modified USP43 increases the amount of CDH2. 2 / 2
| 2

reach
"Therefore, USP43 overexpression in DLD1 cells could promote and inhibit the protein expressions of N-cadherin and Vimentin and protein expressions of N-cadherin, respectively."

reach
"Moreover, USP43 overexpression in DLD1 cells could effectively increase protein expressions of N-cadherin and Vimentin (P < 0.01)."
USP43 increases the amount of CDH2. 2 / 2
| 2

reach
"USP43 knockdown in SW480 cells could effectively inhibit protein expressions of N-cadherin and Vimentin (P < 0.01)."

reach
"Meanwhile, USP43 knockdown in SW480 cells could inhibit and promote the protein expressions of N-cadherin and Vimentin and protein expressions of N-cadherin, respectively."
USP43 affects CDH1
2 | 2
USP43 decreases the amount of CDH1.
| 2
Modified USP43 decreases the amount of CDH1. 1 / 1
| 1

reach
"However, USP43 overexpression in DLD1 cells could effectively inhibit E-cadherin protein expressions (P < 0.01)."
USP43 decreases the amount of CDH1. 1 / 1
| 1

reach
"However, USP43 knockdown in SW480 cells could effectively promote protein expressions of E-cadherin (P < 0.01)."
USP43 binds CDH1.
2 |
1 |

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1 |

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TAFAZZIN affects USP43
| 3 1
TAFAZZIN binds USP43.
| 2 1
| 2 1

sparser
"Immunofluorescence staining and co-immunoprecipitation (Co-IP) assays were used to explore the interaction between USP43 and TAZ."

reach
"Immunofluorescence staining and co-immunoprecipitation (Co-IP) assays were used to explore the interaction between USP43 and TAZ."

reach
"Co-IP and ubiquitination assays revealed that USP43 interacted with and stabilized TAZ by inhibiting TAZ ubiquitination."
TAFAZZIN inhibits USP43.
| 1
| 1

reach
"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."
NuRD affects USP43
| 4
USP43 binds NuRD. 4 / 4
| 4

reach
"The USP43/NuRD complex inhibits the activity of EGFR and AKT, while the EGFR/PI3K/AKT signaling pathway regulates the behavior of USP43."

reach
"Therefore, it has been established that the USP43/NuRD complex inhibits the growth, invasion, and metastasis of breast cancer cells; thus, USP43 may serve as a suppressor of breast cancer."

reach
"Histone H2BK120 can be deubiquitinated by the complex of USP43 and NuRD complex and be reactivated."

reach
"It has been discovered that the USP43/NuRD complex inhibits the expression of numerous cancer-related genes, including the epidermal growth factor receptor (EGFR)."
MTA3 affects USP43
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HDAC2 affects USP43
2 | 1 1
2 | 1 1

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reach
"The interaction between USP43 and HDAC2 was confirmed by Co-IP assay (Fig. 9C)."

sparser
"The interaction between USP43 and HDAC2 was confirmed by Co-IP assay (Fig.  xref C)."

No evidence text available
YWHAH affects USP43
3 |
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USP43 affects pdaC
| 3
USP43 activates pdaC.
| 2
USP43 activates pdaC. 2 / 2
| 2

reach
"High USP43 Expression Promote Proliferation of PDAC."

reach
"Experiments in vitro established that USP43 enhanced the proliferation of PDAC and that the overexpression or knockdown of USP43 promoted or inhibited the proliferation of PDAC, respectively."
USP43 inhibits pdaC.
| 1
USP43 inhibits pdaC. 1 / 1
| 1

reach
"USP43 Inhibits CD8 + T Cell Activation in PDAC."
USP43 affects calcium(2+)
| 3
| 3

reach
"To further investigate if USP43 mediated the function of Ca 2.2 in metastasis in vivo, we transplanted luciferase-tagged MDA-MB-436 cells stably expressing Ca 2.2 shRNA and USP43 cDNA constructs into mice."

reach
"To determine whether USP43 mediated the functions of Ca 2.2, we introduced Ca 2.2 shRNA and USP43 cDNA constructs into breast cancer cells."

reach
"Immunoblotting showed that cortactin expression was stabilized in Ca 2.2 knock-down cells expressing USP43 (Fig. 6A), indicating USP43 mediated the function of Ca 2.2 in cortactin stabilization."
USP43 affects YWHAH
3 |
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USP43 affects Ubiquitin
| 3
USP43 inhibits Ubiquitin.
| 2
| 2

reach
"Mechanically, USP43 activated the Wnt/β-catenin signaling pathway through inhibiting ubiquitin-mediated degradation of HDAC2 to induce EOC cell chemoresistance.USP43 functions as a tumor promoter in multiple cancers."

reach
"USP43 inhibited ubiquitin-mediated degradation of HDAC2 in EOC cells."
USP43 activates Ubiquitin.
| 1
| 1

reach
"Knock-down of USP43 increased the addition of ubiquitin on cortactin (Fig. 5H)."
USP43 affects HDAC1
3 |
3 |

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| 3
USP43 activates Cell Survival.
| 2
| 2

reach
"The results suggested that USP43 knockdown treated SW480 cells could significantly decrease cell survival in three different drug treatments compared with that in normal SW480 cells (P < 0.05)."

reach
"However, USP43 overexpression in DLD1 cells could effectively promote cell survival in three different drug treatments compared with that in normal DLD1 cells (P < 0.05)."
USP43 inhibits Cell Survival.
| 1

reach
"Figure XREF_FIG G and Figure XREF_FIG H suggested that ZEB1 over-expression and knockdown treatments could effectively reverse the changes in cell survival rate caused by USP43 knockdown and overexpression treatment in the chemotherapy sensitivity analysis (P < 0.01)."

reach
"USP43 promotes the proliferation of epithelial ovarian cancer (EOC) and impairs its cisplatin sensitivity."

reach
"Notably, online database studies revealed frequent alterations and/or lack of USP43 in numerous types of cancer, thereby compelling further investigation into its function in the progression of cancer and potential targets as a novel therapeutic approach.Studies in databases and clinicopathological specimens have confirmed that USP43 expression is significantly elevated in breast, pancreatic, lung, bladder, and epithelial ovarian cancers."

reach
"USP43 impairs cisplatin sensitivity in epithelial ovarian cancer through HDAC2-dependent regulation of Wnt/beta-catenin signaling pathway."
HDAC1 affects USP43
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Air Pollutants increases the amount of USP43.
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Air Pollutants increases the amount of USP43. 2 / 2
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Air Pollutants decreases the amount of USP43.
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Air Pollutants decreases the amount of USP43. 1 / 1
1 |

No evidence text available
Vorinostat affects USP43
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Vorinostat increases the amount of USP43. 2 / 2
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Titanium dioxide increases the amount of USP43.
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Titanium dioxide increases the amount of USP43. 1 / 1
1 |

No evidence text available
Titanium dioxide demethylates USP43.
1 |
1 |

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2 |
Pirinixic acid decreases the amount of USP43.
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Pirinixic acid decreases the amount of USP43. 1 / 1
1 |

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Pirinixic acid activates USP43.
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Phenylmercury acetate increases the amount of USP43. 2 / 2
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Paracetamol affects USP43
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Paracetamol decreases the amount of USP43. 2 / 2
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P-chloromercuribenzoic acid increases the amount of USP43. 2 / 2
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Entinostat affects USP43
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Entinostat increases the amount of USP43. 2 / 2
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No evidence text available
2 |
Benzo[a]pyrene methylates USP43.
1 |
1 |

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Benzo[a]pyrene decreases the amount of USP43.
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Benzo[a]pyrene decreases the amount of USP43. 1 / 1
1 |

No evidence text available
2 |
Aflatoxin B1 increases the amount of USP43.
1 |
Aflatoxin B1 increases the amount of USP43. 1 / 1
1 |

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Aflatoxin B1 decreases the amount of USP43.
1 |
Aflatoxin B1 decreases the amount of USP43. 1 / 1
1 |

No evidence text available
YWHAG affects USP43
2 |
2 |

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No evidence text available
| 2

reach
"USP43 knockdown in SW480 cells could significantly inhibit cell migration and invasion compared to that in the normal SW480 cells (P < 0.01)."

reach
"However, USP43 overexpression in DLD1 cells could promote cell migration and invasion compared to that in the normal DLD1 cells (P < 0.01)."
USP43 affects YWHAG
2 |
2 |

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USP43 affects MBD3
2 |
2 |

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USP43 affects Interferon
| 2
USP43 inhibits Interferon.
| 1
| 1

reach
"In the 2 megabases region around MYH13 and MYH8 we found only three genes which could be involved in the fight against SIV: i) Synthaxin 8, a vesicle trafficking protein that functions in the early secretory pathway, ii) USP43 (Ubiquitin-Specific-Processing Protease 43) which negatively regulates type 1 IFN signaling by downregulating the JAK–STAT pathway, iii) ADPRM (ADP-Ribose/CDP-Alcohol Diphosphatase, Manganese Dependent) knockdown of which by shRNA inhibits HIV-1 replication in cultured Jurkat T-cells (PMID: 19460752)."
USP43 decreases the amount of Interferon.
| 1
USP43 decreases the amount of Interferon. 1 / 1
| 1

reach
"This study demonstrated that USP43, as a deubiquitinating enzyme, negatively regulates the expression of type I interferon (IFN) and the Usp43 deficient enhances antiviral innate immune response against VSV infection both in vitro and in vivo."
USP43 affects DOC2B
| 2
| 2

sparser
"The Z-score values of these features were all positive for the DOC2B-USP43 FO sequence (Fig.  xref , bottom right)."

sparser
"For the DOC2B-USP43 FO, analysis of SHAP contribution values revealed that the feature, “Net chrg. per AA”, was the largest positive contributor, and the additional features, “ABT balance”, “ABT valence”, and “Fraction pos."
USP43 affects DNA Damage
| 2
USP43 inhibits DNA Damage.
| 1
| 1

reach
"USP43 suppressed DNA damage and apoptosis, thereby reducing the sensitivity of EOC cells to cisplatin."
USP43 activates DNA Damage.
| 1
| 1

reach
"Given that DNA damage is a most prominent mechanism of cisplatin for cancer treatment [24], we further explored the effect of USP43 on cisplatin-induced DNA damage."
| 1 1
| 1 1

reach
"In addition, high expression of USP43 was accompanied by malignant phenotypes in EOC, suggesting that USP43 promotes tumorigenesis in EOC.Ubiquitination is one of the vital post-translational modifications of proteins, which plays a crucial role in regulation of cell apoptosis [28, 29]."

eidos
"In addition , USP43 could promote tumorigenesis by regulating cell cycle and EMT process in breast cancer 14 ."
USP43 affects CHD4
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USP1 affects USP43
1 | 1
USP1 increases the amount of USP43.
| 1
USP1 increases the amount of USP43. 1 / 1
| 1

reach
"Comparing the mRNA expression of USP1 and USP43 in EWS cell lines from DepMap portal (32), USP1 is overexpressed in EWS cell lines compared with USP43 (Fig. 1C)."
USP1 binds USP43.
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1 |

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Particulate Matter increases the amount of USP43.
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Particulate Matter increases the amount of USP43. 1 / 1
1 |

No evidence text available
Particulate Matter decreases the amount of USP43.
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Particulate Matter decreases the amount of USP43. 1 / 1
1 |

No evidence text available
NFATC4 affects USP43
| 1 1
NFATC4 increases the amount of USP43.
| 1
NFATC4 increases the amount of USP43. 1 / 1
| 1

reach
"We found that depletion of NFAT2 and NFAT3 could significantly reduced USP43 mRNA expression (Fig. 7D, Supplementary Fig. 11)."
NFATC4 binds USP43.
| 1
| 1

sparser
"It is possible that NFAT3 binds to the other regions of USP43 promoter or indirectly regulates USP43 expression."
MBD3 affects USP43
2 |
2 |

No evidence text available

No evidence text available
DOC2B affects USP43
| 2
| 2

sparser
"The Z-score values of these features were all positive for the DOC2B-USP43 FO sequence (Fig.  xref , bottom right)."

sparser
"For the DOC2B-USP43 FO, analysis of SHAP contribution values revealed that the feature, “Net chrg. per AA”, was the largest positive contributor, and the additional features, “ABT balance”, “ABT valence”, and “Fraction pos."
CTTN affects USP43
| 2
| 2

sparser
"We first determined whether USP43 interacted with cortactin."

sparser
"Immunoprecipitation showed that USP43 interacted with cortactin in MDA-MB-231 cells (Fig. xref )."
CHD4 affects USP43
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2 |

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No evidence text available
CDH1 affects USP43
2 |
1 |

No evidence text available
1 |

No evidence text available
AKT affects USP43
| 1 1
AKT phosphorylates USP43.
| 1
AKT phosphorylates USP43. 1 / 1
| 1

rlimsp
"Interestingly, USP43 also exists in the cytoplasm, where it is phosphorylated by AKT, enabling its binding to the 14-3-3β/ε heterodimer and sequestration in the cytoplasm."
AKT activates USP43.
| 1
AKT activates USP43. 1 / 1
| 1

reach
"Phosphorylation by AKT enables USP43 to interact with the 14-3-3β/ε heterodimer and remain localized in the cytoplasm."
6-propyl-2-thiouracil increases the amount of USP43.
1 |
6-propyl-2-thiouracil increases the amount of USP43. 1 / 1
1 |

No evidence text available
6-propyl-2-thiouracil decreases the amount of USP43.
1 |
6-propyl-2-thiouracil decreases the amount of USP43. 1 / 1
1 |

No evidence text available
2 |

No evidence text available

No evidence text available
Vinclozolin affects USP43
1 |
1 |

No evidence text available
Triptonide affects USP43
1 |
Triptonide decreases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Trichloroethene decreases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Tributylstannane increases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Thioacetamide increases the amount of USP43. 1 / 1
1 |

No evidence text available
Tetrachloromethane increases the amount of USP43. 1 / 1
1 |

No evidence text available
Systhane affects USP43
1 |
Systhane increases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Sulforaphane decreases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Sodium lactate increases the amount of USP43. 1 / 1
1 |

No evidence text available
Sodium dodecyl sulfate increases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Sodium arsenite decreases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Rosiglitazone increases the amount of USP43. 1 / 1
1 |

No evidence text available
1 |
Quinolin-8-ol decreases the amount of USP43. 1 / 1
1 |

No evidence text available
Quercetin affects USP43
1 |
Quercetin decreases the amount of USP43. 1 / 1
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No evidence text available
Permethrin affects USP43
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No evidence text available
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No evidence text available
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Panobinostat increases the amount of USP43. 1 / 1
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No evidence text available
Ozone affects USP43
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Ozone increases the amount of USP43. 1 / 1
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No evidence text available
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Nickel monoxide increases the amount of USP43. 1 / 1
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No evidence text available
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Mercury dibromide increases the amount of USP43. 1 / 1
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No evidence text available
Manganese(II) chloride increases the amount of USP43. 1 / 1
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No evidence text available
Leflunomide affects USP43
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Leflunomide increases the amount of USP43. 1 / 1
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No evidence text available
Ketamine affects USP43
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Ketamine decreases the amount of USP43. 1 / 1
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No evidence text available
Jinfukang affects USP43
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Jinfukang decreases the amount of USP43. 1 / 1
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No evidence text available
Inulin affects USP43
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Inulin decreases the amount of USP43. 1 / 1
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No evidence text available
Folic acid affects USP43
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Folic acid demethylates USP43. 1 / 1
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No evidence text available
Dual-luciferase affects USP43
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Dual-luciferase activates USP43. 1 / 1
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reach
"The dual-luciferase reporter assay revealed that exogenous c-Myc significantly increased the activity of the USP43 promoter."
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Dorsomorphin increases the amount of USP43. 1 / 1
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No evidence text available
Domoic acid affects USP43
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Domoic acid increases the amount of USP43. 1 / 1
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No evidence text available
Decabromodiphenyl ether increases the amount of USP43. 1 / 1
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No evidence text available
Cytokine affects USP43
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sparser
"Because USP43 is so tightly associated with cytokines, we looked for which cytokines in the broad cytokine family were related to USP43 and found to be strongly inversely associated with CXCL12 expression ( xref )."
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Clothianidin decreases the amount of USP43. 1 / 1
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No evidence text available
Cisplatin affects USP43
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Cisplatin decreases the amount of USP43. 1 / 1
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No evidence text available
Choline affects USP43
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Choline demethylates USP43. 1 / 1
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No evidence text available
Chloroprene affects USP43
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Chloroprene increases the amount of USP43. 1 / 1
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No evidence text available
Caffeine affects USP43
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Caffeine dephosphorylates USP43. 1 / 1
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No evidence text available
Bis(2-ethylhexyl) phthalate increases the amount of USP43. 1 / 1
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No evidence text available
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Beta-lapachone decreases the amount of USP43. 1 / 1
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No evidence text available
Aristolochic acid A increases the amount of USP43. 1 / 1
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No evidence text available
Acetamide affects USP43
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Acetamide increases the amount of USP43. 1 / 1
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No evidence text available
Abrine affects USP43
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Abrine increases the amount of USP43. 1 / 1
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No evidence text available
YWHAZ affects USP43
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No evidence text available
YWHAQ affects USP43
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No evidence text available
XPO7 affects USP43
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No evidence text available
WDR3 affects USP43
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No evidence text available
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No evidence text available
VPS35 affects USP43
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No evidence text available
USP43 affects migration
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USP43 activates migration. 1 / 1
| 1

eidos
"USP43 could promote cell proliferation , invasion , and migration in colorectal cancer by regulating ZEB1 ubiquitylation degradation ."
USP43 affects migration invasion colorectal cancer
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USP43 activates migration invasion colorectal cancer. 1 / 1
| 1

eidos
"USP43 could promote the proliferation , migration , and invasion of colorectal cancer ."
USP43 affects metastasis colorectal cancer Colorectal cancer
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USP43 activates metastasis colorectal cancer Colorectal cancer. 1 / 1
| 1

eidos
"USP43 directly regulates ZEB1 protein , mediating proliferation and metastasis of colorectal cancer Colorectal cancer is one of the most common malignant tumors of the digestive tract ."
USP43 affects growth metastasis breast cancer
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USP43 inhibits growth metastasis breast cancer. 1 / 1
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eidos
"Meanwhile , previous study indicated that USP43 could remarkably inhibit the growth and metastasis of breast cancer though affecting EGFR / PI3K / AKT 13 ."
USP43 affects cytokine
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sparser
"Because USP43 is so tightly associated with cytokines, we looked for which cytokines in the broad cytokine family were related to USP43 and found to be strongly inversely associated with CXCL12 expression ( xref )."
USP43 affects colorectal cancer cells probe biological function USP43 colorectal cancer cells
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USP43 activates colorectal cancer cells probe biological function USP43 colorectal cancer cells. 1 / 1
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eidos
"USP43 promotes proliferation of colorectal cancer cells in vitro To further probe the biological function of USP43 in colorectal cancer cells , we have studied USP43 expressions in five selected cell lines , including FHC , HCT116 , SW480 , DLD1 , and LOVO ."
USP43 affects cell growth
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reach
"The promoter of nuclear anchoring protein Sun2 (FDR = 0.03 and FDR = 0.002), a lack of which causes cardiac hypertrophy via enhanced AKT/MAPK signaling in the absence of fibrosis, also remained hypermethylated following detraining, as did Usp43 (FDR = 0.0007 and FDR = 0.006), which strongly suppresses cell growth (Figure 3C)."
USP43 affects cell cycle
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reach
"In addition, USP43 could promote tumorigenesis by regulating cell cycle and EMT process in breast cancer XREF_BIBR."
USP43 affects ZEB1 protein
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USP43 inhibits ZEB1 protein. 1 / 1
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eidos
"Moreover , USP43 can reduce ZEB1 protein expression without affecting its transcription ."
USP43 affects YWHAZ
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No evidence text available
USP43 affects YWHAQ
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No evidence text available
USP43 affects XPO7
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No evidence text available
USP43 affects WDR3
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No evidence text available
USP43 affects VPS35
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No evidence text available
USP43 affects USP1
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No evidence text available
USP43 affects TXNL4A
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No evidence text available
USP43 affects TRMT6
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No evidence text available
USP43 affects TRIM56
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No evidence text available
USP43 affects TMEM165
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No evidence text available
USP43 affects TBK1
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USP43 leads to the ubiquitination of TBK1. 1 / 1
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reach
"The USP43/RNF2 axis negatively regulates antiviral innate immunity by promoting TBK1 ubiquitination and degradation."
USP43 affects STX10
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No evidence text available
USP43 affects SSR3
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No evidence text available
USP43 affects SNAI1
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No evidence text available
USP43 affects S
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S binds USP43. 1 / 1
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No evidence text available
USP43 affects S phase
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USP43 activates S phase. 1 / 1
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reach
"USP43 overexpression was observed to induced a decrease in G1-phase and G2-phase cells and an increase in S-phase cells (Fig. 4B)."
USP43 affects RNF2
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USP43 deubiquitinates RNF2. 1 / 1
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"Here, we reveal that E3 ubiquitin ligase ring finger protein 2 (RNF2) is deubiquitinated and stabilized by ubiquitin specific peptidase 43 (USP43) through interactome and quantitative ubiquitinome mass spectrometry analysis."
USP43 affects RFFL
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No evidence text available
USP43 affects RELA
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No evidence text available
USP43 affects RBBP7
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No evidence text available
USP43 affects RBBP4
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No evidence text available
USP43 affects PSME3
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No evidence text available
USP43 affects PSMA2
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No evidence text available
USP43 affects POLD1
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No evidence text available
USP43 affects PDCD2
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No evidence text available
USP43 affects PCNA
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USP43 activates PCNA. 1 / 1
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reach
"Subsequently, deISGylation by USP43 enables PCNA to rebind to replicative DNA polymerases in order to resume normal DNA replication [46]."
USP43 affects PANC02
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USP43 activates PANC02. 1 / 1
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"USP43 overexpression promoted PANC-1 cell proliferation (P = 0.0018), but USP43 knockdown decreased PANC02 cell proliferation (P < 0.001)."
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reach
"Overexpression of the Ubiquitin Specific Proteases USP43, USP41, USP27x and USP6 in Osteosarcoma Cell Lines: Inhibition of Osteosarcoma Tumor Growth and Lung Metastasis Development by the USP Antagonist PR619."
USP43 affects NHS
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No evidence text available
USP43 affects NFATC4
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sparser
"It is possible that NFAT3 binds to the other regions of USP43 promoter or indirectly regulates USP43 expression."
USP43 affects NFATC1
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sparser
"We used Chromatin Immunoprecipitation (ChIP) analysis to further determined the direct interactions of NFAT2 with USP43 promoter in MDA-MB-231 cells, ChIP analysis indicated the significant enrichment of USP43 promoter as well as BMI1 promoter which is a well-established direct target gene of NFAT2 [ xref ] and served as a control in NFAT2 immunoprecipitation (Fig. xref , Supplementary Fig. xref )."
USP43 affects NCOA4
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No evidence text available
USP43 affects MRPS12
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No evidence text available
USP43 affects MBI
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USP43 binds MBI. 1 / 1
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reach
"Given that both USP43 and FBXW7 bind to the MBI of c-Myc, it seems reasonable to assume that increased USP43 may impede FBXW7’s access to c-Myc."
USP43 affects MARCHF5
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No evidence text available
USP43 affects MAPT
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No evidence text available
USP43 affects MAGI3
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No evidence text available
USP43 affects LDHA-luciferase
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USP43 activates LDHA-luciferase. 1 / 1
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reach
"The dual-luciferase reporter assay showed that USP43 could further enhance the activation of LDHA-luciferase by c-Myc (Fig. 1G)."
USP43 affects LCOR
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No evidence text available
USP43 affects K148/289R
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USP43 deubiquitinates K148/289R. 1 / 1
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reach
"Further deubiquitination assays showed that USP43 was able to deubiquitinate wild-type c-Myc but not the c-Myc mutants K148R, K289R, and K148/289R (Fig. 5J)."
USP43 affects INTS1
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No evidence text available
USP43 affects Histone_H3
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USP43 leads to the deacetylation of Histone_H3. 1 / 1
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reach
"Thus, USP43 depletion not only abolishes H2Bub1 deposition but also inhibits H3 deacetylation [ 42 ]."
USP43 affects Histone
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USP43 deubiquitinates Histone. 1 / 1
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reach
"Histone H2BK120 can be deubiquitinated by the complex of USP43 and NuRD complex and be reactivated."
USP43 affects Hippo
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USP43 activates Hippo. 1 / 1
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"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."
USP43 affects HSPA8
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No evidence text available
USP43 affects HSPA1A
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No evidence text available
USP43 affects HRAS
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No evidence text available
USP43 affects HIF1
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USP43 activates HIF1. 1 / 1
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reach
"Mechanistically, USP43 associates with 14-3-3 proteins in a hypoxia and phosphorylation dependent manner to increase the nuclear pool of HIF-1."
USP43 affects HAUS5
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No evidence text available
USP43 affects H2Bub1
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Mutated USP43 inhibits H2Bub1. 1 / 1
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reach
"Remarkably, certain USP43 mutations promote cytoplasmic sequestration of USP43 and/or impaired H2Bub1 removal that compromises EGFR repression."
USP43 affects H2BC3
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No evidence text available
USP43 affects H2B
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No evidence text available
USP43 affects H2AX
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USP43 activates H2AX. 1 / 1
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reach
"In addition, the protein levels of cleaved PARP, cleaved caspase-3 and γH2AX induced by USP43 overexpression were further elevated by silencing HDAC2 (Fig. 10E)."
USP43 affects Flag
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sparser
"Our results demonstrated a strong interaction between exogenously expressed Flag-USP43 and HA-c-Myc in 293 T cells (Fig. xref ), while recombinant GST-c-Myc pulled down recombinant His-USP43 in vitro (Fig. xref )."
USP43 affects FTSJ1
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No evidence text available
USP43 affects FN3KRP
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No evidence text available
USP43 affects EPAS1
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sparser
"No association of endogenous or overexpressed USP43 with HIF-2α was observed (Fig.  xref ), consistent with the HIF-1α specificity observed in the ccRCC lines."
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USP43 deubiquitinates E3_Ub_ligase. 1 / 1
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reach
"Here, we reveal that E3 ubiquitin ligase ring finger protein 2 (RNF2) is deubiquitinated and stabilized by ubiquitin specific peptidase 43 (USP43) through interactome and quantitative ubiquitinome mass spectrometry analysis."
USP43 affects DDX11
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No evidence text available
USP43 affects Cyclin
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USP43 increases the amount of Cyclin. 1 / 1
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reach
"In addition, the expression of CDK4, CDK6 and cyclin D1 was downregulated upon USP43 silencing (Fig. 4C) and upregulated by USP43 overexpression (Fig. 4D), which contributes to cell entry into the proliferation cycle."
USP43 affects CTNNB1
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No evidence text available
USP43 affects CSNK2B
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No evidence text available
USP43 affects CEP57
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No evidence text available
USP43 affects CDK6
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USP43 increases the amount of CDK6. 1 / 1
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reach
"In addition, the expression of CDK4, CDK6 and cyclin D1 was downregulated upon USP43 silencing (Fig. 4C) and upregulated by USP43 overexpression (Fig. 4D), which contributes to cell entry into the proliferation cycle."
USP43 affects CDK5RAP2
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No evidence text available
USP43 affects CDK4
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USP43 increases the amount of CDK4. 1 / 1
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reach
"In addition, the expression of CDK4, CDK6 and cyclin D1 was downregulated upon USP43 silencing (Fig. 4C) and upregulated by USP43 overexpression (Fig. 4D), which contributes to cell entry into the proliferation cycle."
USP43 affects CC
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USP43 activates CC. 1 / 1
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reach
"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."
USP43 affects CASP3
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USP43 activates CASP3. 1 / 1
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reach
"In addition, the protein levels of cleaved PARP, cleaved caspase-3 and γH2AX induced by USP43 overexpression were further elevated by silencing HDAC2 (Fig. 10E)."
USP43 affects BLCA
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USP43 activates BLCA. 1 / 1
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reach
"Moreover, USP43 may stimulate the metastasis of BLCA."
USP43 affects ATG4A
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No evidence text available
USP43 affects AKT
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USP43 bound to NuRD inhibits AKT. 1 / 1
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reach
"The USP43/NuRD complex inhibits the activity of EGFR and AKT, while the EGFR/PI3K/AKT signaling pathway regulates the behavior of USP43."
USP43 affects 7b
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No evidence text available
| DOI
Tobacco Smoke Pollution decreases the amount of USP43. 1 / 1
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No evidence text available
TXNL4A affects USP43
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No evidence text available
TRMT6 affects USP43
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No evidence text available
TRIM56 affects USP43
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No evidence text available
TMEM165 affects USP43
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No evidence text available
Soot affects USP43
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Soot increases the amount of USP43. 1 / 1
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No evidence text available
Smoke affects USP43
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Smoke decreases the amount of USP43. 1 / 1
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No evidence text available
STX10 affects USP43
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No evidence text available
SSR3 affects USP43
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No evidence text available
SNAI1 affects USP43
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No evidence text available
S affects USP43
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S binds USP43. 1 / 1
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No evidence text available
RFFL affects USP43
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No evidence text available
RELA affects USP43
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No evidence text available
RBBP7 affects USP43
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No evidence text available
RBBP4 affects USP43
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No evidence text available
PSME3 affects USP43
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No evidence text available
PSMA2 affects USP43
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No evidence text available
POLD1 affects USP43
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No evidence text available
PDCD2 affects USP43
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No evidence text available
PCB138 affects USP43
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PCB138 increases the amount of USP43. 1 / 1
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No evidence text available
PCB 180 affects USP43
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PCB 180 increases the amount of USP43. 1 / 1
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No evidence text available
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reach
"USP43 potentially regulates cancer invasion by modulating EMT-associated transcription factors, such as ZEB1 or SNAIL, in breast cancer, colorectal cancer, and osteosarcoma."
NHS affects USP43
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No evidence text available
NFATC3 affects USP43
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NFATC3 decreases the amount of USP43. 1 / 1
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reach
"However, the knock-down of NFAT1 and NFAT4 did not decrease USP43 mRNA expression (Supplementary Fig. 12)."
NFATC2 affects USP43
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NFATC2 decreases the amount of USP43. 1 / 1
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reach
"However, the knock-down of NFAT1 and NFAT4 did not decrease USP43 mRNA expression (Supplementary Fig. 12)."
NFAT affects USP43
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NFAT increases the amount of USP43. 1 / 1
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reach
"We then investigated whether NFAT proteins were able to modulate USP43 mRNA expression."
NCOA4 affects USP43
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No evidence text available

No evidence text available
MRPS12 affects USP43
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No evidence text available
MBI affects USP43
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USP43 binds MBI. 1 / 1
| 1

reach
"Given that both USP43 and FBXW7 bind to the MBI of c-Myc, it seems reasonable to assume that increased USP43 may impede FBXW7’s access to c-Myc."
MARCHF5 affects USP43
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No evidence text available
MAPT affects USP43
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No evidence text available
MAGI3 affects USP43
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No evidence text available
LCOR affects USP43
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No evidence text available
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L-methionine demethylates USP43. 1 / 1
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No evidence text available
INTS1 affects USP43
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No evidence text available
HSPA8 affects USP43
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No evidence text available
HSPA1A affects USP43
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No evidence text available
HRAS affects USP43
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No evidence text available
HAUS5 affects USP43
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No evidence text available
H2BC3 affects USP43
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No evidence text available
H2B affects USP43
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No evidence text available
Gentamicins affects USP43
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Gentamicins decreases the amount of USP43. 1 / 1
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No evidence text available
Flag affects USP43
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sparser
"Our results demonstrated a strong interaction between exogenously expressed Flag-USP43 and HA-c-Myc in 293 T cells (Fig. xref ), while recombinant GST-c-Myc pulled down recombinant His-USP43 in vitro (Fig. xref )."
FTSJ1 affects USP43
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No evidence text available
FN3KRP affects USP43
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No evidence text available
FBXW7 affects USP43
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reach
"In BLCA, DNA polymerase POLD1 and the ubiquitin-specific protease USP43 competitively bind to MYC, preventing its interaction with FBXW7 and thereby stabilizing MYC protein levels."
EPAS1 affects USP43
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sparser
"No association of endogenous or overexpressed USP43 with HIF-2α was observed (Fig.  xref ), consistent with the HIF-1α specificity observed in the ccRCC lines."
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Dietary Fats increases the amount of USP43. 1 / 1
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No evidence text available
DDX11 affects USP43
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No evidence text available
CTNNB1 affects USP43
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No evidence text available
CSNK2B affects USP43
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No evidence text available
CEP57 affects USP43
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No evidence text available
CDK5RAP2 affects USP43
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No evidence text available
ATG4A affects USP43
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No evidence text available
AKT1 affects USP43
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AKT1 phosphorylates USP43. 1 / 1
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reach
"Based on the current understanding, P-AKT can phosphorylate numerous downstream effectors, including USP43, GSK3, FOXO1, which influences chromatin remodeling ( He et al., 2018 ), glucose metabolism, [MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
7b affects USP43
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No evidence text available
| DOI
2-hydroxypropanoic acid increases the amount of USP43. 1 / 1
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No evidence text available
1,2-dimethylhydrazine increases the amount of USP43. 1 / 1
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No evidence text available
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No evidence text available
2,4,4'-trichlorobiphenyl increases the amount of USP43. 1 / 1
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No evidence text available
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No evidence text available
1 |

No evidence text available