IndraLab

Statements


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"Functional experimental results showed that USP47 promoted the cell proliferation in vitro and tumor growth in vivo ."

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"Ubiquitin-specific peptidase 47 expression is elevated in many tumors and is involved in multiple expression regulating mechanisms, including transcriptional, post-transcriptional, and post-translational modifications."

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"Furthermore, we identify Snai1 as a deubiquitination target of USP47, explaining USP47-dependent activation of the epithelial-mesenchymal transition pathway and tumor progression."

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"Furthermore, xenograft assays demonstrated that silencing USP47 can inhibit LUSC tumor growth in vivo."

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"Consistent with in vitro results, USP47 knockdown drastically inhibited tumor growth in vivo (Figure 2F and Supplemental Figure 6F)."

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"Conversely, USP47 overexpression markedly accelerated tumor growth, yielding larger tumors and higher weights (Supplemental Figure 7, I and J)."

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"Thus , the findings here indicate that USP47 can promote tumor proliferation by regulating levels of p53 ."

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"Overexpression of USP47 could reduce the tumor inhibition induced by LINC00668 knockout (Hu et al., 2019)."

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"USP47 subsequently stabilizes Snail by deubiquitination and promotes EMT and tumor metastasis (35)."

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"Previous reports indicated that USP47 promotes colorectal cancer EMT and malignancy by stabilizing Snail and activating the Wnt signaling pathway [ 64 ] ."

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"Knockdown of USP47 induces CDC25A accumulation and the inhibition of tumor growth."

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"Yu et al also reported that USP47 and SMURF2 can mediate CC cell proliferation and tumor progression by reversibly manipulating SATB1 ubiquitination."