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首页> 外文期刊>Experimental and therapeutic medicine >Overexpression of microRNA-936 suppresses non-small cell lung cancer cell proliferation and invasion via targeting E2F2
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Overexpression of microRNA-936 suppresses non-small cell lung cancer cell proliferation and invasion via targeting E2F2

机译:MicroRNA-936的过表达抑制了非小细胞肺癌细胞增殖和侵袭靶向E2F2

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摘要

MicroRNA (miR)-936 has been reported to inhibit the cell cycle and glioma cell proliferation. However, the roles of miR-936 in other human tumors remain largely unknown. In the present study, it was indicated that miR-936 was significantly downregulated in non-small cell lung cancer (NSCLC) tissues compared with adjacent normal tissues by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Results also indicated that miR-936 was downregulated in NSCLC cell lines compared with 16HBE cells. Furthermore, it was demonstrated that overexpression of miR-936 significantly inhibited the proliferation, cell cycle progression and invasion of NSCLC cells. Notably, E2F2 was identified as a target gene of miR-936 in NSCLC cells. The results indicated that E2F2 was upregulated in NSCLC tissues and cell lines, and its expression was negatively correlated with that of miR-936 in NSCLC tissues. Overexpression of miR-936 significantly reduced the protein expression levels of E2F2 in NSCLC cells. Furthermore, restoration of E2F2 rescued the proliferation and invasion of NSCLC cells transfected with miR-936 mimics. To the best of our knowledge, the present findings demonstrated for the first time that miR-936 suppressed NSCLC progression by directly targeting E2F2.
机译:据报道,MicroRNA(miR)-936抑制细胞周期和胶质瘤细胞增殖。然而,MIR-936在其他人类肿瘤中的作用仍然很大程度上是未知的。在本研究中,表明,通过逆转录定量聚合酶链反应(RT-QPCR)与相邻的正常组织相比,在非小细胞肺癌(NSCLC)组织中,MIR-936显着下调。结果还表明,与16HBE细胞相比,MIR-936在NSCLC细胞系中下调。此外,证明MIR-936的过表达显着抑制了NSCLC细胞的增殖,细胞周期进展和侵袭。值得注意的是,E2F2被鉴定为NSCLC细胞中miR-936的靶基因。结果表明,E2F2在NMSCLC组织和细胞系中升高,其表达与NSCLC组织中的miR-936的表达呈负相关。 miR-936的过表达显着降低了NSCLC细胞中E2F2的蛋白质表达水平。此外,E2F2的恢复救出了用miR-936模仿转染的NSCLC细胞的增殖和侵袭。据我们所知,本研究结果首次证明了MIR-936通过直接靶向E2F2来抑制NSCLC进展。

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