IndraLab

Statements


USP27X activates HYCC1. 8 / 8
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"We also found that the levels of SETD3 and USP27 increased significantly in HCC than those in the relevant adjacent tissues."

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"These results indicate that depletion of USP27 also inhibited HCC cell growth in vivo."

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"Furthermore, evidence from in vitro and in vivo studies revealed that depletion of USP27 inhibited HCC cell proliferation, invasion, metastasis and tumorigenesis, and that overexpression of SETD3 rescued this phenotype."

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"USP27 knockdown inhibits HCC cell growth in vivo."

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"In vivo studies confirmed that USP27 knockdown suppresses HCC growth and metastasis."

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"In conclusion, USP27X‐AS1 upregulated AKT protein expression by recruiting USP7 to deubiquitinate AKT.3.6 USP27X-AS1 promoted HCC progression by regulating AKT."

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"To verify whether USP27X‐AS1 promoted HCC progression via AKT, we transfected Flag‐AKT into USP27X‐AS1 knockdown cells and used AKT‐siRNA to interfere with AKT expression in USP27X‐AS1 overexpressed cells."

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"To unravel the mechanism by which USP27X‐AS1 promotes HCC, we conducted RNA‐seq on HLF cells with USP27X‐AS1 overexpression and the control counterparts."