IndraLab

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USP43 activates cell population proliferation. 21 / 21
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"For instance, USP43 promoted cell proliferation, migration and invasion of colorectal cancer [12]."
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"USP43 could promote the proliferation, migration, and invasion of colorectal cancer."
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"USP43 promotes proliferation of colorectal cancer cells in vitro."
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"For cell proliferation analysis, USP43 knockdown in SW480 cells could significantly reduce cell proliferation compared with those in normal SW480 cells on days 2, 3, 4, 5 (P < 0.01)."
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"Overexpression of TAZ reversed the inhibitory effects of USP43 silencing on CC cell proliferation, migration, invasion and EMT CONCLUSION: USP43 promotes CC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) by activating the Hippo/TAZ pathway."
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"USP43 overexpression promoted EOC cell proliferation, enhanced the ability of migration and invasion, decreased cisplatin sensitivity and inhibited apoptosis."
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"USP43 could promote cell proliferation , invasion , and migration in colorectal cancer by regulating ZEB1 ubiquitylation degradation ."
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"USP43 promoted cell proliferation, migration, invasion and chemoresistance of EOC."
38087046
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"Overexpression of USP43 significantly increased cell proliferation (Fig. 3D and F)."
38087046
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"USP43 overexpression promoted PANC-1 cell proliferation (P = 0.0018), but USP43 knockdown decreased PANC02 cell proliferation (P < 0.001)."
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"Furthermore, USP43 was highly expressed in colorectal cancer (CRC) and increased CRC cell proliferation, invasion, and migration [23]."
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"In EOC, USP43 promotes the proliferation and impairs cisplatin sensitivity."
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"Silencing of USP43 reduced cell proliferation, migration, invasion, and the epithelial-mesenchymal transition (EMT) process."
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"However, USP43 overexpression in DLD1 cells could significantly promote cell proliferation compared with those in vector treated DLD1 cells on days 2, 3, 4, 5 (P < 0.05)."
33391437
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"USP43 knockdown in SW480 cells could significantly reduce cell proliferation."
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"Meanwhile, USP43 overexpression in DLD1 cells could significantly promote cell proliferation in vitro."
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"Meanwhile, Figure XREF_FIG C and XREF_FIG D suggested that knockdown and over-expression treatment of ZEB1 gene treatments could effectively inhibit and promote cell proliferation caused by USP43 overexpression and knockdown treatments, respectively."
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"USP43 promotes the proliferation of epithelial ovarian cancer (EOC) and impairs its cisplatin sensitivity."
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"High USP43 Expression Promote Proliferation of PDAC."
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"The study delves into the tumor-promoting impact in EOC, showing that USP43 enhances the proliferation, invasion, and migration of EOC, and facilitates EOC cells to enter the cell cycle’s proliferation phase.Cisplatin is a primary chemotherapeutic treatment for EOC."
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"Experiments in vitro established that USP43 enhanced the proliferation of PDAC and that the overexpression or knockdown of USP43 promoted or inhibited the proliferation of PDAC, respectively."
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