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Inhibition of autophagy potentiates the proliferation inhibition activity of microRNA-7 in human hepatocellular carcinoma cells

机译:抑制自噬可增强microRNA-7在人肝癌细胞中的增殖抑制活性

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摘要

MicroRNAs (miRNAs/miRs) are important molecules that are able to regulate multiple cellular processes in cancer cells. miR-7 has been previously identified as a tumor suppressive miRNA in several types of cancer. The aim of the present study was to investigate whether miR-7 is able to regulate autophagy in hepatocellular carcinoma (HCC) cells. It was identified that miR-7 was significantly downregulated in tumor tissues compared with adjacent normal tissues. Overexpression of miR-7 inhibited cell proliferative activity, which was partially reversed by miR-7 inhibitor. In addition, overexpression of miR-7 significantly induced an increasen in autophagic activity, and luciferase activity assay and western blot analysis identified that mammalian target of rapamycin (mTOR) was a direct target of miR-7. In addition, inhibition of autophagy by 3-methyladenine resulted in a marked enhancement of the proliferation inhibition effect of miR-7. In conclusion, miR-7 was identified to induce proliferation inhibition and autophagy in HCC cells by targeting mTOR, and inhibition of autophagy may be utilized to enhance the antitumor activity of miR-7.
机译:微小RNA(miRNA / miRs)是重要的分子,能够调节癌细胞中的多个细胞过程。 miR-7先前已被鉴定为几种类型癌症中的抑癌miRNA。本研究的目的是研究miR-7是否能够调节肝细胞癌(HCC)细胞中的自噬。已确定与邻近的正常组织相比,miR-7在肿瘤组织中显着下调。 miR-7的过表达抑制细胞增殖活性,miR-7抑制剂可部分逆转该增殖活性。此外,miR-7的过表达显着诱导了自噬活性的增加,荧光素酶活性测定和Western blot分析表明,哺乳动物雷帕霉素靶标(mTOR)是miR-7的直接靶标。此外,3-甲基腺嘌呤抑制自噬导致miR-7的增殖抑制作用显着增强。总之,已确定通过靶向mTOR来诱导miR-7诱导HCC细胞的增殖抑制和自噬,并且可以利用对自噬的抑制来增强miR-7的抗肿瘤活性。

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