IndraLab

Statements



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"Proliferation inhibition by loss of USP10 depends on SKP2 functional status."

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"HDAC7 promotes NSCLC proliferation and metastasis via stabilization by deubiquitinase USP10 and activation of β-catenin-FGF18 pathway."

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"Interesting, Spautin‐1 imposed minimal effect on the cell proliferation (Fig. S5C), suggesting that under our experimental conditions, USP10 mainly modulated cell migration rather than cell proliferation, through the regulatory effect on Smad4."

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"USP10 regulates Musashi-2 stability via deubiquitination and promotes tumour proliferation in colon cancer."

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"We found that loss of USP10 consequently suppressed the proliferation of CML cells and induced G0/G1 phase arrest in all CML cell lines examined, suggesting that USP10 is critical to CML cell proliferation."

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"Targeting USP10 by shRNA inhibited CRC proliferation and metastasis, and this effect was reversed by overexpression of NLRP7."

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"As shown in XREF_FIG, downregulation of USP10 increased cancer cell proliferation in p53 +/+ cells, while USP10 expression levels have no apparent effect on proliferation in cells lacking p53."

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"Moreover, inhibition of USP10 significantly suppresses the proliferation of both imatinib sensitive and imatinib resistant CML cells, which likely depends on SKP2 status."

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"Paradoxically, USP10 could promote cancer cell proliferation in mutant p53 background."

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"Moreover, we have also experimentally demonstrated that both pharmacological and genetic inhibition of USP10 are capable of, in a SKP2-depednet manner, suppressing the proliferation of both IM sensitive and IM resistant CML cells in cell cultures and in mouse xenograft models."

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"Two independent USP10 short hairpin RNAs (shRNAs) both promoted cell proliferation of HCCLM3 and HUH7 cells."

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"In vitro data showed that USP10 deficiency reduced proliferation and migration of rat thoracic aorta smooth muscle cells (A7r5) and human aortic smooth muscle cells (HASMCs)."

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"Indeed, downregulation of USP10 decreases p53 stability and increases cancer cell proliferation XREF_BIBR, thus projecting a role as a tumor suppressor."

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"In conclusion, these results suggest that USP10 promotes proliferation and migration and inhibits apoptosis of endometrial stromal cells in endometriosis through activating the Raf-1/MEK/ERK pathway."

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"USP10 promotes proliferation and migration and inhibits apoptosis of endometrial stromal cells in endometriosis through activating the Raf-1/MEK/ERK pathway."

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"For example, in hepatocellular carcinoma, Zhu et al. reported that USP10 promotes proliferation [XREF_BIBR], whereas Lu et al. found that USP10 suppresses tumor progression by inhibiting mTOR activation [XREF_BIBR]."

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"Specifically, USP10 activates PTEN by preventing its K63 linked polyubiquitination mediated by TRIM25 and suppresses the AKT and mTOR signaling pathway thereby inhibiting NSCLC proliferation, indicating that it may be a potential drug target for cancer treatment."

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"USP10 overexpression promoted ectopic endometrial stromal cell migration and proliferation, suppressed cell apoptosis, and activated MEK and ERK signaling that is a critical downstream target of the serine/threonine protein kinase Raf-1, which was significantly blocked by PD98059."

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"For example, in p53-mutant RCC cells, increased USP10 expression promotes cell proliferation via deubiquitinating and stabilizing the mutant p53 [27]."

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"In RCC cell lines that have mutant p53, USP10 promotes cancer cell proliferation, and downregulation of USP10 would be beneficial for the inhibition of cancer growth."