IndraLab

Statements



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"Our results revealed that knockdown of OTUD6B significantly impaired the viability, clonal expansion, and proliferation of LUAD cells (Fig. 2C–G)."

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"One study found that OTUD6B drives the G1/S transition and promotes the proliferation of multiple myeloma cells by suppressing microRNA biogenesis via LIN28B stabilization [ 11 ]."

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"Using nude mice and AMC–HN–8 as the representative cell lines, we explored how OTUD6B modulated in vivo proliferation of the tumor cells."

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"In CCA cells, OTUD6B knockdown reduced CCA cell proliferation and promoted apoptosis."

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"In the current study, using AMC–HN–8 and TU177 cells as representative LSCC models, we confirmed that OTUD6B overexpression enhanced the proliferation of LSCC in vitro and in vivo ."

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"In addition, lung cancer cell lines with OTUD6B knockdown significantly inhibited proliferation and invasion ability of lung cancer cells."

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"It is also obvious that OTUD6B silencing inhibited the proliferation, migration, and invasion of A549 and Pc9 cells ( Figures 10C–E )."

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"OTUD6B knockdown inhibited the proliferation of LUAD cells and enhanced apoptosis and inhibited metastasis in LUAD cells suppressed."

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"We found that activation of Otud6b expression with rOtud6b increased endothelial cell inflammation and apoptosis, smooth muscle cells inflammation and proliferation."

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"OTUD6B knockdown inhibited the proliferation of LUAD cells."

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"OTUD6B depletion also led to a G1/S arrest and reduced proliferation in cancer cells of epithelial origin such as A549 lung adenocarcinoma cells, suggesting a more general role of OTUD6B in promoting cell cycle progression (Fig EV2A–C)."