IndraLab

Statements

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"USP39 overexpression deprived miR-133a inhibitor mediated suppression of cell proliferation, suggesting that USP39 is involved in miR-133a-mediated biological role in gastric cancer cell HGC-27 (P < 0.0001) (XREF_FIG)."
29805563
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"Wang et al. [21] also found that USP39 was highly expressed in breast cancer cells, and down-regulation of USP39 could significantly reduce the proliferation and colony formation of breast cancer cells."
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"Knockdown of USP39 significantly inhibited proliferation of TT cells in vitro."
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"Knockdown of USP39 significantly decreased cell proliferation and caused cell cycle arrest at G2/M phase."
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"We further observed that USP39 downregulation inhibits the cell proliferation and migration of A549 and HCC827 cells."
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"USP39 downregulation could inhibit RCC cell proliferation and progression, suggesting that USP39 may prove to be a potential target for inhibiting RCC."
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"Moreover, USP39 depletion inhibits HCC cell proliferation and metastasis by promoting ZEB1 degradation."
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"Furthermore, knockdown of USP39 inhibited VSMC cell proliferation and the expression of cyclin D1 and cyclin-dependent kinase 4, as analyzed via cell counting, MTT assay and western blotting."
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"In addition, it has been reported that overexpression of MGC-803 cells and knockdown of USP39 may inhibit MGC-803 cell proliferation and induce cell cycle arrest."
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"Knockdown of USP39 suppressed the proliferation and cell cycle progression, and induced apoptosis, accompanied by the reduction of EGFR in both mRNA and protein levels in PC-3 and DU145 cells."
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"Knockdown of USP39 remarkably inhibited the cell proliferation of osteosarcoma cells."
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"Down-regulation of USP39 suppresses the proliferation and induces the apoptosis of human colorectal cancer cells [XREF_BIBR]."
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"Down-regulation of USP39 inhibited cell proliferation and colony formation ability of SMMC-7721 cells."
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"The SUMOylation of spliceosome factors USP39 decreases the proliferation enhancing effect of USP39 on prostate cancer cells."
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"Knockdown of USP39 expression in U2OS cell significantly decreased cell proliferation, impaired colony formation ability."
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