首页> 外文期刊>Anti-cancer drugs >Artesunate induces G0/G1 cell cycle arrest and iron-mediated mitochondrial apoptosis in A431 human epidermoid carcinoma cells
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Artesunate induces G0/G1 cell cycle arrest and iron-mediated mitochondrial apoptosis in A431 human epidermoid carcinoma cells

机译:青蒿琥酯诱导A431人表皮样癌细胞中G0 / G1细胞周期阻滞和铁介导的线粒体凋亡

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摘要

The anticancer effects of artesunate (ART) have been well documented. However, its potential against skin cancer has not been explored yet. Herein we reported that 60 μmol/l ART effectively inhibited A431 (human epidermoid carcinoma cells) growth but not that of HaCaT (normal human keratinocyte cells). Our results revealed that ART induced cell cycle arrest at G0/G1 phase through the downregulation of cyclin A1, cyclin B, cyclin D1, Cdk2, Cdk4, and Cdk6. This correlated with the upregulation of p21 and p27. The 5-bromodeoxyuridine incorporation assay also indicated that ART treatment reduced DNA synthesis in a time-dependent manner. Furthermore, ART induced mitochondrial apoptosis, as evidenced by annexin V/propidium iodide staining and western blot analysis. Interestingly, ART-induced apoptosis diminished under iron-deficient conditions but intensified under iron-overload conditions. Taken together, these findings demonstrated the potential of ART in treating skin cancer through the induction of G0/G1 cell cycle arrest and iron-mediated mitochondrial apoptosis and supported further investigations in other test systems.
机译:青蒿琥酯(ART)的抗癌作用已得到充分证明。但是,尚未发现其抗皮肤癌的潜力。本文中我们报道了60μmol/ l ART有效抑制A431(人表皮样癌细胞)的生长,但不能抑制HaCaT(正常人角质形成细胞)的生长。我们的结果表明,ART通过下调细胞周期蛋白A1,细胞周期蛋白B,细胞周期蛋白D1,Cdk2,Cdk4和Cdk6诱导G0 / G1期细胞周期停滞。这与p21和p27的上调相关。 5-溴脱氧尿苷掺入测定还表明,ART处理以时间依赖性方式减少了DNA的合成。此外,如膜联蛋白V /碘化丙啶染色和蛋白质印迹分析所证明,ART诱导线粒体凋亡。有趣的是,在铁缺乏的条件下,ART诱导的凋亡减少,但在铁超载的条件下,凋亡加剧。综上所述,这些发现证明了ART通过诱导G0 / G1细胞周期停滞和铁介导的线粒体细胞凋亡治疗皮肤癌的潜力,并支持其他测试系统的进一步研究。

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