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首页> 外文期刊>International journal of oncology >Tanshinone IIA induces cytochrome?c-mediated caspase cascade apoptosis in A549 human lung cancer cells via the JNK pathway
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Tanshinone IIA induces cytochrome?c-mediated caspase cascade apoptosis in A549 human lung cancer cells via the JNK pathway

机译:丹参酮IIA通过JNK途径诱导A549人肺癌细胞中细胞色素c介导的caspase级联凋亡

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Tanshinone?IIA (TSIIA), a natural diterpene quinone in the traditional Chinese medicinal herb Dan-Shen (Salvia?miltiorrhiza), has extensively exerted antitumor activity in cellular and animal models. However, the molecular mechanisms underlying the antitumor effects of TSIIA remain largely unknown. The in?vitro effects of TSIIA on apoptosis were investigated in A549 non-small cell lung cancer (NSCLC) cells. The data showed that TSIIA significantly suppressed the proliferation of A549 cells in a dose-dependent manner, with IC50 values of 16.0±3.7 and 14.5±3.3?μM at 48?h as determined by Cell Counting Kit-8 (CCK-8) assay and clone formation assay, respectively. The change of mitochondrial morphology and the loss of mitochondrial membrane potential (MMP) were observed during the induction. Furthermore, TSIIA induced A549 cell apoptosis as confirmed by typical morphological changes, with cytochrome?c release from the mitochondria and Bax translocation to the mitochondria. Caspase activity data indicated that TSIIA activated caspase-9 and caspase-3 of mitochondria-mediated apoptosis, but not caspase-8 of receptor-mediated apoptosis, which could be largely rescued by SP600125 (JNK inhibitor). Taken together, these findings provide the first evidence that TSIIA inhibits growth of NSCLC A549 cells, induces activation of JNK signaling and triggers caspase cascade apoptosis mediated by the release of cytochrome?c, which provides a better understanding of the molecular mechanisms of TSIIA on lung cancer.
机译:丹参酮IIA(TSIIA)是传统中草药丹参(Salvia?miltiorrhiza)中的天然二萜醌,已在细胞和动物模型中广泛发挥抗肿瘤活性。然而,TSIIA的抗肿瘤作用的分子机制仍是未知之数。在A549非小细胞肺癌(NSCLC)细胞中研究了TSIIA对细胞凋亡的体外作用。数据显示TSIIA以剂量依赖性方式显着抑制A549细胞的增殖,通过细胞计数试剂盒8(CCK-8)测定,在48?h时IC50值为16.0±3.7和14.5±3.3?μM。和克隆形成试验。诱导过程中观察到线粒体形态的变化和线粒体膜电位(MMP)的损失。此外,TSIIA诱导了A549细胞凋亡,这一点已通过典型的形态学改变得到证实,细胞色素从线粒体中释放出来,并且Bax易位到线粒体中。 Caspase活性数据表明,TSIAA激活了线粒体介导的凋亡的caspase-9和caspase-3,但没有激活受体介导的凋亡的caspase-8,这可以通过SP600125(JNK抑制剂)大量挽救。综上所述,这些发现提供了第一个证据,TSIIA抑制NSCLC A549细胞的生长,诱导JNK信号的激活,并触发由细胞色素?c释放介导的半胱天冬酶级联凋亡,从而更好地了解了TSIIA在肺部的分子机制。癌症。

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