IndraLab

Statements

SIRT7 activates USP39. 6 / 6
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"Besides, SIRT7 promotes autophagy and inhibits oxidative stress in cervical squamous cell carcinoma cells by regulating the USP39/FOXM1 axis [23]."
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"SIRT7 promotes USP39 protein stability via deacetylation at the site K428, and USP39 facilitates the splicing efficacy of FOXM1 to elevate FOXM1 expression."
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"Moreover, SIRT7 has been demonstrated to deacetylate USP39, increasing the stability, and promoting the oncogenic activity of USP39 in hepatocellular carcinoma development [24]."
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"These results indicate that SIRT7 promotes the stability of USP39 via deacetylation."
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"In the above experiment, we have shown that SIRT7 interacts with USP39 and enhance protein stability of USP39 via deacetylation and that USP39 regulates SIRT7 expression."
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"Furthermore, SIRT7 increases the stability of USP39 by means of direct deacetylation."
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