IndraLab

Statements

USP37 activates Neoplasm Invasiveness. 16 / 16
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"XREF_BIBR Therefore, it is possible that IH mediated miR-320b reduction in lung cancer cells resulted in the upregulation of USP37, which further promoted cancer cell proliferation, invasion, and survival."
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"Further studies indicated that USP37 knockdown could inhibit the stemness, cell invasion and EMT in breast cancer via downregulation of Hh pathway."
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"The knockdown of USP37 could inhibit the stemness, cell invasion and EMT via downregulation of Hedgehog pathway."
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"Moreover, we found that knockdown of USP37 suppressed cell migration and invasion in breast cancer cells."
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"We previously demonstrated that ubiquitin carboxyl-terminal hydrolase 37 (UCH37), a member of the DUBs, promoted invasion and postoperative recurrence of HCC, and pre-mRNA processing factor 19 (Prp19) may function as its downstream effecter [XREF_BIBR]."
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"USP37 knockdown suppresses breast cancer cell migration and invasion by promoting mesenchymal-epithelial transition."
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"On the contrary, upregulation of USP37 promoted EMT, migration and invasion."
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"In contrast , USP37 upregulation promotes EMT , migration , and invasion [ 39 ] ."
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"Furthermore, upregulation of USP37 markedly promoted invasion and migration of breast cancer cells (Fig. 3k and l)."
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"In contrast, USP37 upregulation promotes EMT, migration, and invasion [39]."
| PMC
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"On the contrary , upregulation of USP37 promoted EMT , migration and invasion ."
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"USP37 in breast cancer was reported to increase cell stemness, epithelial‐mesenchymal transition (EMT), and invasion, while to decrease the sensitivity to cisplatin."
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"USP37 knockdown suppresses breast cancer cell migration and invasion by promoting mesenchymal-epithelial transition Currently , the underlying biological mechanism accounting for the elevated expression of USP37 in breast tumors remains unclear ."
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"USP37-activated SALL4 might enhance keloid fibroblast growth, invasion, migration, ECM accumulation and glycolysis via activating PI3K/AKT pathway."
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"USP37 up-regulation promoted the proliferation, cell cycle progression, apoptosis inhibition, migration, invasion, epithelial mesenchymal transition (EMT) and stemness of CRC cells; moreover, USP37 facilitated the angiogenesis of human umbilical vein endothelial cells (HUVECs)."
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"Accumulating evidence has demonstrated that USP37 promotes lung cancer cell proliferation, migration, and invasion XREF_BIBR but inhibits lung cancer cell apoptosis in a deubiquitination dependent manner."
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