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

机译:抑制自噬增强了人肝细胞癌细胞中microRNA-7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:MicroRNA(miRNA / mirs)是能够调节癌细胞中多种细胞过程的重要分子。 MiR-7之前已被鉴定为若干类型的癌症中的肿瘤抑制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。与相邻的正常组织相比,鉴定了MIR-7在肿瘤组织中显着下调。 MIR-7的过度表达抑制细胞增殖活性,其由miR-7抑制剂部分反转。此外,MIR-7的过表达显着诱导在自噬活性方面增加,并且荧光素酶活性测定和蛋白质污染物分析鉴定出哺乳动物的哺乳动物毒素(MTOR)的靶标是miR-7的直接靶标。此外,通过3-甲基腺嘌呤抑制自噬导致miR-7的增殖抑制效果明显增强。总之,通过靶向MTOR鉴定MIR-7以诱导HCC细胞中的增殖抑制和自噬,并且可以利用自噬抑制来增强miR-7的抗肿瘤活性。

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