IndraLab
Statements
sparser
"Ubiquitin-specific protease 33 (USP33)/VDU1 was also shown to be involved in ROBO1–USP33 interaction and participate in SLIT/ROBO signaling in cancer cell migration. xref Another study also showed that srGAP1 is an important downstream molecule of Slit2 signaling in CRC, and mediates the antimigration function of Slit2 by inhibiting Cdc42. xref SrGAP2 protein expression is reduced or absent in a subset of primary osteosarcoma samples, srGAP2 and other axon guidance proteins likely play a role in osteosarcoma metastasis. xref "
reach
"USP33 promotes the generation of excessive centriolar foci due to elevated levels of CP110 because (1) over-expression of human or murine USP33 led to CP110 up-regulation in multiple cell lines (XREF_SUPPLEMENTARY) and (2) depletion of CP110 overrode USP33 mediated generation of centriolar foci (XREF_SUPPLEMENTARY)."
USP33 affects cell population proliferation
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30
USP33 activates cell population proliferation.
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18
USP33 inhibits cell population proliferation.
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12
USP33 affects Neoplasm Invasiveness
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1
27
USP33 activates Neoplasm Invasiveness.
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USP33 activates Neoplasm Invasiveness. 10 / 19
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1
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"As shown in Fig. 3A, compared with other ECM components, the binding ability of USP33-overexpressed cells was significantly increased in the laminin (which is also the primary component of Matrigel) group, indicating that USP33-mediated invasion may be related to the inducement of the adhesiveness to laminin."
USP33 inhibits Neoplasm Invasiveness.
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9
sparser
"The proteasome has both ubiquitin ligases and DUBs that associate with it (Crosas et al., 2006) , and several DUB-ligase pairs interact directly, including BRCC36-BRCA1, BAP1-BRCA1, USP4-Ro52, USP7-MDM2, USP8-GRAIL, USP20-pVHL, USP33-pVHL and USP44-APC (Kee and Huibregtse, 2007; Marfany and Denuc, 2008; Ventii and Wilkinson, 2008) ."
reach
"Mechanistically, USP33 deubiquitinated and stabilized the TGFBR2 protein in PC cells and therefore enhanced the signaling of TGF-β pathway, USP33 removed the K63-linked ubiquitin conjugates from TGFBR2 and prevented its degradation by lysosome, meanwhile, USP33 promoted the recycling of TGFBR2 to cell membrane and eventually enhanced the signaling in TGF-β pathway."
reach
"Our results suggested that USP33 knockdown inhibited the expression of TGFBR2 protein, the overexpression of USP33 had the opposite effect on TGFBR2 protein while no alteration was observed in TGFBR2 mRNA after the manipulation on USP33 expression (Fig. 5E–G), all these results indicated that USP33 may participate in the posttranslational modification of TGFBR2."
sparser
"The proteasome has both ubiquitin ligases and DUBs that associate with it (Crosas et al., 2006) , and several DUB-ligase pairs interact directly, including BRCC36-BRCA1, BAP1-BRCA1, USP4-Ro52, USP7-MDM2, USP8-GRAIL, USP20-pVHL, USP33-pVHL and USP44-APC (Kee and Huibregtse, 2007; Marfany and Denuc, 2008; Ventii and Wilkinson, 2008) ."
USP33 affects Neoplasm Metastasis
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1
20
USP33 activates Neoplasm Metastasis.
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1
17
USP33 inhibits Neoplasm Metastasis.
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3
USP33 affects cell migration
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14
USP33 activates cell migration.
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11
USP33 activates cell migration. 10 / 12
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11
reach
"We found that integrin α6 and USP33 overexpression in USP33-knockdown cells can largely rescue cell migration abilities on laminin in both KYSE-150 and KYSE-450 cells compared to indicated knockdown cells (Fig. 5C), which highlights the importance of integrin α6 in USP33-mediated ESCC cell migration on laminin."
USP33 inhibits cell migration.
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3
USP33 affects Pancreatic Neoplasms
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13
USP33 activates Pancreatic Neoplasms.
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12
USP33 activates Pancreatic Neoplasms. 10 / 12
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12
reach
"To assess whether USP33 affected the invasiveness and migration of PC cells, we performed the transwell migration and invasion assays and found that USP33 knockdown significantly inhibited the migration and invasiveness of PC cells while USP33 overexpression showed the opposite effect (Fig. 2H–J)."
USP33 inhibits Pancreatic Neoplasms.
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1
USP33 inhibits Pancreatic Neoplasms. 1 / 1
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1
MiR-365a-3p affects USP33
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10
MiR-365a-3p activates USP33.
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7
reach
"To further verify that miR-365a-3p directly targets and downregulates USP33, the wild-type 3 ' UTR of USP33 (WT USP33 3 ' UTR) or a mutated USP33 3 ' UTR (Mut USP33 3 ' UTR) was cloned into a dual-luciferase UTR vector and then co-transfected with agomiR-365 or a negative control (agomiR-NC) into A549 and SPC-A-1 cells."
MiR-365a-3p inhibits USP33.
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2
MiR-365a-3p binds USP33.
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1
sparser
"Thus, it could be speculated that AKT exerts two distinct effects on the homologous desensitization of GPCRs: one mechanism involves AKT regulating receptor desensitization by promoting the nuclear entry of Mdm2, while an alternative mechanism involves the promotion of the interaction of USP33 with β-arrestin."
sparser
"The association of USP33 and β-arrestin 2 itself appears to be dependent on the class of 7TMR as activation of the β2-adrenergic receptor (β2AR), a Class A receptor known to have a transient interaction with β-arrestins, enhances the association of β-arrestin 2 with USP33 [ xref ]."
sparser
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL)- interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of β-mercaptoethanol, which dissociates selenium (Jeong et al., xref ), suggesting a selenium dependent interaction of SELENBP1 and VDU1."
reach
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL) - interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of beta-mercaptoethanol, which dissociates selenium, suggesting a selenium dependent interaction of SELENBP1 and VDU1."
sparser
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL)- interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of β-mercaptoethanol, which dissociates selenium (Jeong et al., xref ), suggesting a selenium dependent interaction of SELENBP1 and VDU1."
reach
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL) - interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of beta-mercaptoethanol, which dissociates selenium, suggesting a selenium dependent interaction of SELENBP1 and VDU1."
USP33 is modified
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8
sparser
"Indeed, biochemical changes in cellular components constituting the GPCR desensitization cascade were evoked when cells were treated with EGF, such as phosphorylation of Src (Fig. xref A), Akt (Fig. xref B), the interaction between Akt and USP33 (Fig. xref C), which culminated in the deubiquitination of arrestins (Fig. xref D)."
reach
"2 min treatment with quinpirole facilitated TRAF6 nuclear entry (Fig. 5A) and AKT nuclear export (Fig. 7A), supporting the temporal correlation between these processes.A recent study revealed that AKT regulates the desensitization of D -like receptors by phosphorylating the deubiquitinase USP33 [17]."
USP33 affects apoptotic process
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6
USP33 affects Slit-Robo
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6
sparser
"Following disease progression on this trial, genomic testing revealed an FGFR2-USP33 fusion, and she subsequently started a basket trial for the FGFR-selective inhibitor pemigatinib where she exhibited a partial response with a 43% reduction in tumor size (NCT02393248) and remained on therapy for 28 months (Fig. xref , Supplementary Figs. xref , xref , xref ) xref ."
sparser
"Following disease progression on this trial, genomic testing revealed an FGFR2-USP33 fusion, and she subsequently started a basket trial for the FGFR-selective inhibitor pemigatinib where she exhibited a partial response with a 43% reduction in tumor size (NCT02393248) and remained on therapy for 28 months (Fig. xref , Supplementary Figs. xref , xref , xref ) xref ."
Lipopolysaccharide affects USP33
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5
Lipopolysaccharide activates USP33. 5 / 5
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5
reach
"In addition, the activation of JAK2/STAT3 by coumermycin A1 remarkably reversed the protective role of miR-206 in LPS-induced inflammatory injuries, suggesting JAK2/STAT3 signaling was a key downstream pathway of miR-206/USP33 in SCM.In this study, our data revealed that miR-206 alleviated LPS-induced inflammatory injuries by directly targeting USP33 and suppressing the activation of JAK2/STAT3 signaling pathway."
reach
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45] ."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
sparser
"Indeed, biochemical changes in cellular components constituting the GPCR desensitization cascade were evoked when cells were treated with EGF, such as phosphorylation of Src (Fig. xref A), Akt (Fig. xref B), the interaction between Akt and USP33 (Fig. xref C), which culminated in the deubiquitination of arrestins (Fig. xref D)."
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
reach
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45] ."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
USP33 affects laminin
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4
reach
"We found that integrin α6 and USP33 overexpression in USP33-knockdown cells can largely rescue cell migration abilities on laminin in both KYSE-150 and KYSE-450 cells compared to indicated knockdown cells (Fig. 5C), which highlights the importance of integrin α6 in USP33-mediated ESCC cell migration on laminin."
USP33 affects glycolytic process
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4
USP33 affects cell growth
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4
USP33 inhibits cell growth.
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2
USP33 activates cell growth.
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2
reach
"Mechanistically, USP33 deubiquitinated and stabilized the TGFBR2 protein in PC cells and therefore enhanced the signaling of TGF-β pathway, USP33 removed the K63-linked ubiquitin conjugates from TGFBR2 and prevented its degradation by lysosome, meanwhile, USP33 promoted the recycling of TGFBR2 to cell membrane and eventually enhanced the signaling in TGF-β pathway."
USP33 affects Slit
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4
E3_Ub_ligase affects USP33
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3
1
E3_Ub_ligase ubiquitinates USP33.
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1
1
E3_Ub_ligase increases the amount of USP33.
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1
E3_Ub_ligase increases the amount of USP33. 1 / 1
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1
E3_Ub_ligase decreases the amount of USP33.
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1
E3_Ub_ligase decreases the amount of USP33. 1 / 1
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1
USP33 affects α-SMA
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3
USP33 affects integrin α6
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3
USP33 affects cell adhesion
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3
USP33 affects arrestins
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3
USP33 deubiquitinates arrestins.
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2
USP33 binds arrestins.
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1
USP33 inhibits USP33.
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2
USP33 increases the amount of USP33.
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1
reach
"Our results suggested that USP33 knockdown inhibited the expression of TGFBR2 protein, the overexpression of USP33 had the opposite effect on TGFBR2 protein while no alteration was observed in TGFBR2 mRNA after the manipulation on USP33 expression (Fig. 5E–G), all these results indicated that USP33 may participate in the posttranslational modification of TGFBR2."
USP33 affects Slit2-Robo1
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3
reach
"Several downstream effectors, including Abl [XREF_BIBR], Dock [XREF_BIBR], Ena (32), ERK1/2 [XREF_BIBR], small Rho GTPases [XREF_BIBR], USP33 [XREF_BIBR] and Vilse [XREF_BIBR], have been reported to mediate the inhibitory effect of Slit2-Robo1 signaling on cell motility, proliferation, apoptosis and angiogenesis in different cell types."
USP33 affects Robo1 receptor
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3
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
USP33 affects Cell Survival
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1
2
USP33 activates Cell Survival.
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1
1
USP33 inhibits Cell Survival.
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1
USP33 inhibits Cell Survival. 1 / 1
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1
Robo1 receptor affects USP33
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3
MiR-206 affects USP33
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2
Integrin α6 affects USP33
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2
Dihydroartemisinin affects USP33
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2
Dihydroartemisinin decreases the amount of USP33. 2 / 2
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2
USP33 affects β2-adrenergic receptor
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2
USP33 affects signal transduction
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2
USP33 affects pyroptosis
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2
USP33 activates pyroptosis. 2 / 2
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2
USP33 affects pathway
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2
USP33 affects miR-206
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2
USP33 affects hydroxyproline
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2
USP33 affects glioma cell migration
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2
USP33 affects beta-arrestins
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2
USP33 affects beta-arrestin
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2
USP33 affects ISG75
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2
USP33 affects Hemagglutinins
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2
USP33 affects Glioblastoma
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2
USP33 affects (S)-lactic acid
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2
Hemagglutinins affects USP33
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2
Vasopressin affects USP33
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1
Vasopressin activates USP33. 1 / 1
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1
SiUSP33 affects USP33
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1
reach
"Using lipid nanoparticle (LNP) encapsulation of siUSP33 by adjusting the lipid components (ionizable cationic lipids), siUSP33 is successfully delivered to mouse lung tissues, rapidly reducing USP33 expression in the lungs and maintaining knockdown for at least 14 days, effectively suppressing viral replication and virulence."
SiUSP33#4 affects USP33
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1
Selenium atom affects USP33
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1
USP33 binds selenium atom. 1 / 1
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1
Rapamycin treatment affects USP33
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1
MiR-590 affects USP33
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1
Laminin affects USP33
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1
reach
"Given the similar findings here, further investigation is needed to elucidate the specific laminin isoform implicated in the stimulation of USP33-mediated ESCC cell metastasis.Considering that accumulating evidence highlights the crucial role of USP33 in multiple cancer development and progression, effects have been undertaken to study the possibility of targeting USPs for cancer therapeutics (Dewson et al. 2023)."
Hydroxyurea affects USP33
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1
Hydroxyurea activates USP33. 1 / 1
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1
Circ0057558 affects USP33
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1
Beta-Arr2 affects USP33
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1
Arrestins affects USP33
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1
Arrestin affects USP33
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1
reach
"For instance, USP33 has been shown to be negatively regulated by p97, the p97 is responsible for HERC2-mediated polyubiquitination of USP33 (Chan et al. 2014), highlighting the HERC2-p97-axis-mediated ubiquitin-proteasome system (UPS) may be a potential target for USP33 degradation, which needs further investigation."
USP33 affects β
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1
USP33 affects β ‐adrenergic receptors
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1
USP33 affects β -AR recycling
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1
USP33 affects vasopressin receptor
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1
USP33 activates vasopressin receptor. 1 / 1
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1
USP33 affects vasodilation
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1
USP33 activates vasodilation. 1 / 1
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1
USP33 affects type 2 deiodinase
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1
USP33 affects stability cellular ATF3 protein
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1
USP33 affects selenium atom
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1
USP33 binds selenium atom. 1 / 1
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1
USP33 affects proteolysis
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1
USP33 inhibits proteolysis. 1 / 1
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1
USP33 affects post-endocytic sorting receptor endosomes autophagosomes
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1
USP33 affects polyubiquitination
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1
USP33 affects pVHL-E3 ligase
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1
USP33 affects p-SMAD2/3
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1
USP33 affects neuron migration
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1
USP33 activates neuron migration. 1 / 1
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1
USP33 affects microtubule polymerization
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1
USP33 activates microtubule polymerization. 1 / 1
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1
USP33 affects miR-365a-3p
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1
USP33 affects iodothyronine deiodinase
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1
USP33 activates iodothyronine deiodinase. 1 / 1
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1
USP33 affects invasion metastasis cells
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1
USP33 affects hydroxyurea
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1
USP33 inhibits hydroxyurea. 1 / 1
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1
USP33 affects glioblastoma multiforme cancer stem cell
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1
USP33 affects docetaxel anhydrous
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1
USP33 inhibits docetaxel anhydrous. 1 / 1
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1
USP33 affects colorectal57 breast58 cancer cell migration
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1
USP33 affects cellular component biogenesis
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1
USP33 activates cellular component biogenesis. 1 / 1
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1
USP33 affects c-Myc ubiquitination
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1
USP33 affects c-Myc protein
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1
USP33 affects beta2AR
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1
USP33 affects beta-Arr2
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1
USP33 affects arrestin
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1
USP33 affects Ubiquitination
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1
USP33 inhibits Ubiquitination. 1 / 1
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1
reach
"Among these proteins, ubiquitin‐specific peptidase 33 (USP33) removes K63‐linked ubiquitin chains, destabilizing Parkin and suppressing mitophagy [33], Conversely, USP8 is capable of removing the K6‐linked ubiquitination from Parkin, thus stabilizing the protein and promoting mitophagy [51], Thus, targeting distinct Parkin ubiquitination modifications yields different outcomes."
USP33 affects USP33-CBX2
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1
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
USP33 affects TGFBP2
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1
USP33 affects Slit Robo signaling pathway
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1
USP33 affects SCF cyclin
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1
USP33 affects Roundabout signaling pathway
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1
USP33 inhibits Roundabout signaling pathway. 1 / 1
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1
USP33 affects Robo
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1
USP33 affects ROBO1 receptor
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1
USP33 affects ROBO
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1
USP33 affects RNA binding protein
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1
USP33 affects Phosphatase
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1
USP33 deubiquitinates Phosphatase. 1 / 1
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1
USP33 affects KO cells
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1
USP33 affects ISG65
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1
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
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1
USP33 activates Esophageal Squamous Cell Carcinoma. 1 / 1
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1
USP33 affects E3 ubiquitin
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1
USP33 affects DUSP1 domain
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1
USP33 affects DNA Damage
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1
USP33 activates DNA Damage. 1 / 1
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1
USP33 affects ARs
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1
USP33 affects 7TMR
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1
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
USP20 affects ARs
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1
USP inhibitor affects USP33
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1
TGFBR2 affects DUSP1 domain
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1
RT-qPCR affects USP33
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1
RNA binding protein affects USP33
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1
Infections affects USP33
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1
Infections decreases the amount of USP33. 1 / 1
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1
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
DUSP1 domain affects USP33
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1
reach
"DIO2 works as a dimer that associates with Hedgehog inducible ubiquitin ligase WD repeat and SOCS box containing 1 (WSB-1) [XREF_BIBR], ubiquitin conjugases UBC6 and UBC-7 [XREF_BIBR], and DIO2 specific deubiquitinating enzymes ubiquitin specific peptidase 20 (USP20), and ubiquitin specific peptidase 33 (USP33) [XREF_BIBR]."
Class A receptor affects USP33
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1
reach
"The association of USP33 and beta-arrestin 2 itself appears to be dependent on the class of 7TMR as activation of the beta2-adrenergic receptor (beta2AR), a Class A receptor known to have a transient interaction with beta-arrestins, enhances the association of beta-arrestin 2 with USP33 [XREF_BIBR]."
CQ affects USP33
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1
Arrestins affects USP33
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1
ARs affects USP33
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1
ARRB affects 7TMR
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1
AD-VDU1 f affects USP33
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1
7TMR affects USP33
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1
(R)-noradrenaline affects USP33
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1
(R)-noradrenaline activates USP33. 1 / 1
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1