首页> 外文期刊>Cancer biology & therapy >Downregulation of XIAP and induction of apoptosis by the synthetic cyclin-dependent kinase inhibitor GW8510 in non-small cell lung cancer cells.
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Downregulation of XIAP and induction of apoptosis by the synthetic cyclin-dependent kinase inhibitor GW8510 in non-small cell lung cancer cells.

机译:非小细胞肺癌细胞中XIAP的下调和合成细胞周期蛋白依赖性激酶抑制剂GW8510诱导的凋亡。

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摘要

Small-molecule inhibitors of cyclin-dependent kinases (CDKs) are known to induce cell cycle arrest and apoptosis in certain cancer cells. In order to evaluate the antitumor activity of one such inhibitor, GW8510, against human lung cancers, we analyzed the effects of GW8510 on six nonsmall cell lung cancer (NSCLC) cell lines (A549, H1299, H460, H226, H358 and H322) and normal human fibroblast (NHFB). We treated the cells with GW8510 at concentrations of 0-10 microM, and found that it suppressed cell growth in vitro in all the lung cancer cells but not in NHFB. Subsequent study showed that GW8510 induced apoptosis and cell cycle arrest in the A549, H1299 and H460 cells in a time- and dose-dependent manner. Western blot analysis showed that GW8510 downregulated the expression of X-linked inhibitor of apoptosis (XIAP) but had no detectable effect on the expression of Bax, Bak, or Bcl2. GW8510 also downregulated XIAP mRNA level, suggesting that downregulation of XIAP expression occurs at the transcriptional level. Moreover, ectopic XIAP expression diminished growth inhibition and apoptosis induction by GW8510. Importantly, GW8510 was not capable of inducing apoptosis of NHFB cells. These results suggest that GW8510 might provide a treatment strategy for human NSCLC and XIAP is an important target for GW8510-induced apoptosis of NSCLC cells that occurs through inhibition of XIAP mRNA transcription.
机译:已知细胞周期蛋白依赖性激酶(CDK)的小分子抑制剂在某些癌细胞中诱导细胞周期停滞和凋亡。为了评估一种这样的抑制剂GW8510对人肺癌的抗肿瘤活性,我们分析了GW8510对六种非小细胞肺癌(NSCLC)细胞系(A549,H1299,H460,H226,H358和H322)的作用,并正常人成纤维细胞(NHFB)。我们用浓度为0-10 microM的GW8510处理细胞,发现它在所有肺癌细胞中均能抑制细胞生长,但在NHFB中却不能。随后的研究表明,GW8510以时间和剂量依赖性方式诱导A549,H1299和H460细胞凋亡和细胞周期停滞。蛋白质印迹分析表明,GW8510下调了X连锁凋亡抑制剂(XIAP)的表达,但对Bax,Bak或Bcl2的表达没有可检测的影响。 GW8510还下调XIAP mRNA水平,表明XIAP表达下调发生在转录水平。此外,异位XIAP表达减少了GW8510的生长抑制和凋亡诱导。重要的是,GW8510不能诱导NHFB细胞凋亡。这些结果表明,GW8510可能为人类NSCLC提供治疗策略,而XIAP是GW8510诱导的通过抑制XIAP mRNA转录而引起的NSCLC细胞凋亡的重要靶标。

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