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Over-expression of DNA-PKcs in renal cell carcinoma regulates mTORC2 activation HIF-2α expression and cell proliferation

机译:DNA-PKcs在肾细胞癌中的过表达调节mTORC2激活HIF-2α表达和细胞增殖

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摘要

Here, we demonstrated that DNA-PKcs is over-expressed in multiple human renal cell carcinoma (RCC) tissues and in primary/established human RCCs. Pharmacological or genetic inhibition of DNA-PKcs suppressed proliferation of RCC cells. DNA-PKcs was in the complex of mTOR and SIN1, mediating mTORC2 activation and HIF-2α expression in RCC cells. Inhibiting or silencing DNA-PKcs suppressed AKT Ser-473 phosphorylation and HIF-2α expression. In vivo, DNA-PKcs knockdown or oral administration of the DNA-PKcs inhibitor NU-7441 inhibited AKT Ser-473 phosphorylation, HIF-2α expression and 786-0 RCC xenograft growth in nude mice. We showed that miRNA-101 level was decreased in RCC tissues/cells, which could be responsible for DNA-PKcs overexpression and DNA-PKcs mediated oncogenic actions in RCC cells. We show that DNA-PKcs over-expression regulates mTORC2-AKT activation, HIF-2α expression and RCC cell proliferation.
机译:在这里,我们证明了DNA-PKcs在多种人肾细胞癌(RCC)组织和原发/已建立的人RCC中过表达。 DNA-PKcs的药理或遗传抑制作用抑制了RCC细胞的增殖。 DNA-PKcs在mTOR和SIN1的复合物中,介导RCC细胞中mTORC2激活和HIF-2α表达。抑制或沉默DNA-PKcs可抑制AKT Ser-473磷酸化和HIF-2α表达。在体内,敲除DNA-PKcs抑制剂NU-7441或口服给予DNA-PKcs抑制裸鼠体内AKT Ser-473磷酸化,HIF-2α表达和786-0 RCC异种移植的生长。我们表明,miRNA-101水平在RCC组织/细胞中降低,这可能是RCC细胞中DNA-PKcs过表达和DNA-PKcs介导的致癌作用的原因。我们表明DNA-PKcs的过度表达调节mTORC2-AKT激活,HIF-2α表达和RCC细胞增殖。

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