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RNA interference-mediated secretory clusterin gene silencing inhibits proliferation and promotes apoptosis of human non-small cell lung cancer cells

机译:RNA干扰介导的分泌簇蛋白基因沉默抑制人非小细胞肺癌细胞增殖并促进其凋亡

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Background/Aims: Non-small cell lung cancer (NSCLC) constitutes around 85% of lung cancer cases and is frequently beyond surgical intervention. Methodology: Secretory clusterin (sCLU) is found in diverse types of human cancers and is unregulated in a variety of cell lines in response to stress, and enhances cancer cell survival. However, the roles of sCLU in NSCLC are still to be elucidated. Results: Here we show that RNA interference (RNAi)-mediated sCLU gene silencing with short interference RNA (siRNA) strongly decreased the sCLU mRNA and protein levels, as well as suppressed cell proliferation and induced cell apoptosis. In addition, sCLU siRNA also blocked the PI3K/AKT signaling pathway, and decreased the AKT phosphorylation level, but no change was found in total AKT level. More importantly, PI3K/AKT signaling pathway inhibitor, LY294002, also reduced tumor cell proliferation, which is similar to the result with or without sCLU siRNA treatment. Conclusions: These results suggest that sCLU plays a positive role in NSCLC cell proliferation, which may be mediated by the PI3K/AKT signaling pathway. Our work in this study demonstrates RNAi-mediated sCLU gene silencing may provide a novel therapeutic strategy in the treatment of NSCLC.
机译:背景/目的:非小细胞肺癌(NSCLC)约占肺癌病例的85%,并且通常超出了手术干预范围。方法:分泌簇蛋白(sCLU)存在于多种类型的人类癌症中,响应压力,在各种细胞系中不受调控,并提高了癌细胞的存活率。然而,仍需阐明sCLU在NSCLC中的作用。结果:在这里,我们表明RNA干扰(RNAi)介导的sCLU基因沉默与短干扰RNA(siRNA)大大降低了sCLU mRNA和蛋白质水平,以及抑制细胞增殖和诱导细胞凋亡。此外,sCLU siRNA还阻断了PI3K / AKT信号通路,并降低了AKT磷酸化水平,但总AKT水平未发现变化。更重要的是,PI3K / AKT信号通路抑制剂LY294002也减少了肿瘤细胞的增殖,这与有或没有sCLU siRNA治疗的结果相似。结论:这些结果表明,sCLU在NSCLC细胞增殖中起积极作用,这可能是由PI3K / AKT信号通路介导的。我们在这项研究中的工作表明,RNAi介导的sCLU基因沉默可能为NSCLC的治疗提供新的治疗策略。

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