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Docetaxel inhibits SMMC-7721 human hepatocellular carcinoma cells growth and induces apoptosis

机译:多西紫杉醇抑制SMMC-7721人肝癌细胞的生长并诱导细胞凋亡

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AIM: To investigate the in vitro anti-hepatocellular carcinoma (HCC) activity of docetaxel against SMMC-7721 HCC cells and its possible mechanism. METHODS: The HCC cells were given different concentrations of docetaxel and their growth was measured by colony forming assay. Cell cycle and apoptosis were analyzed by flow cytometry and fluorescence microscopy (acridine orange/ethidium bromide double staining, AO/EB), as well as electronic microscopy. The SMMC-7721 HCC cell reactive oxygen species (ROS) and glutathione (GSH) were measured after given docetaxel. RESULTS: Docetaxel inhibited the hepatocellular carcinoma cells growth in a concentration dependent manner with IC_(50)5x10~(-10) M. Marked cell apoptosis and G2/M phase arrest were observed after treatment with docetaxel ≥10~(-8)M. Docetaxel promoted SMMC-7721 HCC cells ROS generation and GSH deletion. CONCLUSION: Docetaxel suppressed the growth of SMMC-7721 HCC cells in vitro by causing apoptosis and G2/M phase arrest of the human hepatoma cells, and ROS and GSH may play a key role in the inhibition of growth and induction of apoptosis.
机译:目的:探讨多西紫杉醇对SMMC-7721 HCC细胞的体外抗肝癌活性及其可能的机制。方法:给肝癌细胞给予不同浓度的多西他赛,并通过集落形成法测定其生长。通过流式细胞术和荧光显微镜(ac啶橙/溴化乙锭双染色,AO / EB)以及电子显微镜分析细胞周期和凋亡。给予多西他赛后,测量SMMC-7721 HCC细胞的活性氧(ROS)和谷胱甘肽(GSH)。结果:多西他赛以IC_(50)5x10〜(-10)M浓度依赖性抑制肝癌细胞的生长。多西他赛≥10〜(-8)M处理后观察到明显的细胞凋亡和G2 / M期阻滞。 。多西他赛可促进SMMC-7721 HCC细胞的ROS生成和GSH缺失。结论:多西紫杉醇可通过诱导人肝癌细胞凋亡和G2 / M期阻滞而抑制SMMC-7721 HCC细胞的生长,ROS和GSH可能在抑制其生长和诱导细胞凋亡中起关键作用。

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