IndraLab

Statements

USP10 inhibits Cell Survival. 7 / 7
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"USP10 inhibits NSCLC cell viability, proliferation, and migration."
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"Furthermore, depletion of USP10 in lung cancer cells causes decreased apoptosis and increased cell survival upon treatment with DNA-damaging agents."
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"It has been reported that knockdown of USP10 in lung cancer cells causes increased cell survival and decreased apoptosis upon treatment with a DNA-methylating and antimetabolite agent (13)."
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"As shown in Figure 6A, USP10 prominently decreased NSCLC cell viability as assayed by 3-(4,5-dimethylthylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT)."
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"Biologically, silenced USP10 in lung cancer cells contributes to the elongated cell survival and depressed apoptosis, partially through deubiquitinating the mismatch repair protein MSH2 [XREF_BIBR], or negatively modulating EIF4G1 mediated functions [XREF_BIBR]."
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"Our findings indicated that USP10 depletion, under the condition of lnc-NR3C overexpression, enhanced cell survival following oxidative stress."
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"Their results show that the depletion of USP10 in A549 increased cell survival and decreased apoptosis through destabilizing MSH2 [32]."
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