IndraLab

Statements



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"In contrast, genetic or chemical inhibition of USP5 leads to CCND1 degradation, thereby resulting in decreased NSCLC cell proliferation and tumor growth."

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"Targeting USP5 suppresses AKT/mTOR/4EBP1 signaling and reduces the proliferation and growth of AML cells."

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"Our experiments further confirmed that USP5 knockdown could suppress ovarian cell proliferation both in vitro and in vivo."

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"The siRNA-induced knockdown of Usp5 inhibited cell proliferation, migration ability and drug resistance."

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"This study showed genetic ablation of USP5 significantly inhibited the viability and proliferation of bladder cancer cells."

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"Down-regulation of USP5 inhibited cell proliferation of ovarian cancer cells."

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"As shown in Figure 3B, NC had little effect on USP5 expression compared to the Control group, and USP5 shRNAs (#1, #2 and #4) reduced USP5 protein expression in both cell lines.Following USP5 shRNAs (#1 and #2) transduction, the proliferation of both cancer cell lines was determined using CCK-8 assays, which showed that down-regulation of USP5 caused profoundly reduced proliferation of both ovarian cancer cell lines (Figure 3C, P<0.001)."

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"Genetic ablation of USP5 markedly inhibited bladder cancer cell proliferation, viability, and migration both in vitro and in vivo."

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"Regarding the proliferative capacity of the cells, the CCK-8 experiments demonstrated that USP5 overexpressing T24 cells had significantly increased proliferation and USP5 knockdown T24 cells had significantly decreased proliferation compared with the control group (P<0.05; Fig. 2D)."

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"A series of phenotypic experiments showed that USP5 overexpression attenuated the inhibition of proliferation and invasion of Huh‐7 and HCC‐LM3 cells in the absence of METTL5 (Supplementary Figure S17)."

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"PTB knockdown causes a decrease in USP5 isoform 2 and an increase in USP5 isoform 1, which further inhibits cell proliferation [ 60 ]."

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"These chalcone derivatives effectively inhibit the activity of DUB, such as USP5, UCH-L3, USP2, UCH-L1, and USP8, leading to irreversible cell cycle arrest in breast, ovarian, and cervical cancer cells (IC50 = 1.5-12.5 µM), as well as inhibiting their proliferation and initiating apoptosis."