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首页> 外文期刊>Oncology letters >miR-101 sensitizes A549 NSCLC cell line to CDDP by activating caspase 3-dependent apoptosis
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miR-101 sensitizes A549 NSCLC cell line to CDDP by activating caspase 3-dependent apoptosis

机译:miR-101通过激活caspase 3依赖性凋亡使A549 NSCLC细胞系对CDDP敏感

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MicroRNA-101 (miR-101) is evidently downregulated in several types of cancer, including non-small cell lung cancer (NSCLC), and is crucial in sensitizing cells to chemotherapy drugs. The aim of the present study was to investigate the correlation between miR-101 and chemosensitivity in the A549 NSCLC cell line. Here, we used the human A549 cell line for transfection with an miR-101 overexpressing vector and detected the cytotoxic acticity, proliferation and apoptosis of cis-diaminedichloroplatinum (CDDP) in A549-miR-101 and A549-mock cells. We demonstrated that overexpression of miR-101 sensitized A549 cells to CDDP, one of the most frequently used agents in curing or controlling NSCLC and enhanced CDDP-induced cell death and caspase 3-dependent apoptosis. In addition, miR-101 facilitated the inhibitory role of CDDP in A549 cell colony formation. Overall, the results of the present study demonstrated that miR-101 sensitizes the A549 NSCLC cell line to CDDP via the activation of caspase 3-dependent apoptosis.
机译:MicroRNA-101(miR-101)在包括非小细胞肺癌(NSCLC)在内的几种类型的癌症中明显下调,并且在使细胞对化疗药物敏感方面起着至关重要的作用。本研究的目的是研究miR-101与A549 NSCLC细胞系化学敏感性之间的相关性。在这里,我们使用人类A549细胞系与miR-101过表达载体进行转染,并检测了A549-miR-101和A549-mock细胞中顺式二胺二氯铂(CDDP)的细胞毒作用,增殖和凋亡。我们证明,miR-101的过度表达使A549细胞对CDDP敏感,CDDP是治疗或控制NSCLC的最常用药物之一,并增强了CDDP诱导的细胞死亡和caspase 3依赖性细胞凋亡。另外,miR-101促进了CDDP在A549细胞集落形成中的抑制作用。总体而言,本研究的结果表明,miR-101通过激活caspase 3依赖性细胞凋亡使A549 NSCLC细胞系对CDDP敏感。

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