IndraLab
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USP22 activates epithelial to mesenchymal transition. 26 / 26
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"These results suggested that overexpression USP22 induced EMT in lung adenocarcinoma cells.Moreover it is well known that TGF-beta1 stimulates the EMT in lung cancer cells [43]."
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"Previous studies have also shown that USP22 can promote tumor progression and induce EMT in various tumors [ 13 , 23 ] ."
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"A more recently published report indicates that USP22 may promote tumor progression and induce EMT in colorectal carcinoma patients [ 13 ] ."
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"These findings indicate that USP22 promotes CRC invasion and metastasis by inducing EMT via AP4 activation."
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"According to the results of previous studies, USP22 can induce EMT by regulating TGF-beta1 in lung cancer cells [XREF_BIBR], and elevated USP22 expression can promote EMT by up-regulating ZEB1 and Snail in pancreatic cancer cells though a process that involves focal adhesion kinase (FAK) signaling [XREF_BIBR]."
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"In vitro study revealed that USP22 can regulate proliferation and invasive properties, and induce EMT of lung adenocarcinoma cells."
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"In vitro, USP22 overexpression promoted the EMT process of NRK-52E cells stimulated by HG and further increased the levels of extracellular matrix (ECM) components such as fibronectin, Collagen I, and Collagen Ⅳ."
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"These results suggested that overexpression USP22 may cause EMT in lung adenocarcinoma cells."
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"USP22 overexpression enhanced the extracellular acidification rate, proliferation, spheroid number, CD44+/CD24- cell number, and the expression of stemness genes and EMT-related markers in TNBC/DDP cells, while these effects were restrained by glycolysis inhibitors."
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"Therefore, USP22 silencing impairs ATC cell migration and invasion by ablating EMT."
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"In the context of EMT induction, miR-30e is an important EMT inhibitor that works by targeting ITGB1, TUSC3, USP22, and SOX9 mRNAs, which reportedly induce EMT by activating transcription factors including SNAIL, SLUG, TWIST, and ZEB1/2 [XREF_BIBR, XREF_BIBR, XREF_BIBR, XREF_BIBR]."
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"Subsequent experiments showed that USP22 knockdown resulting from up-regulation of miR-30e-5p could inhibit proliferation, invasion, migration, and EMT in 5-8F cells."
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"Moreover, we evaluated whether USP22 could induce EMT in cultured lung cancer cells."
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"In addition, we present evidence that USP22 promotes Bel/Fu cell growth, migration, invasion, EMT and chemoresistance."
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"Taken together, these results indicate that USP22 increases cell migration and invasion by inducing EMT by binding to the promoter of AP4 to activate its transcription."
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"To explore the role of AP4 in the promotion of EMT by USP22, we knocked down AP4 in USP22-down-regulated cells to detect the changes in the expression levels of key factors involved in EMT."
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"These results indicate that USP22 increases CRC cell migration and invasion abilities by promoting EMT."
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"Our in-depth examination demonstrated that AP4 acts as a downstream molecule of USP22 and is required for the promotion of EMT by USP22 and the increased migration and invasion of CRC cells."
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"USP22 Contributes to Chemoresistance, Stemness, and EMT Phenotype of Triple-Negative Breast Cancer Cells by egulating the Warburg Effect via c-Myc Deubiquitination."
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"Moreover, USP22 overexpression can promote EMT and TGF-beta expression, whereas USP22 knockdown can reverse EMT and reduce the metastasis of lung adenocarcinomas."
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"The present study has revealled an additional novel mechanism by which USP22 induces EMT."
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"Aberrant USP22 expression can promote tumor progression and induce EMT in lung ADC [16, 19]."
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"USP22 downregulation inhibited OS cell proliferation , invasion , and epithelial-mesenchymal transition ( EMT ) in vitro ."
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"However, the functional role of USP22 as a DUB may also be a critical contributor to the process of USP22 induced EMT via epigenetic regulation, emphasizing the need to explore the epigenetic functions of USP22 in CRC metastasis."