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首页> 外文期刊>Cell biochemistry and biophysics >Tegillarca granosa Extract Haishengsu Induces Apoptosis in Human Hepatocellular Carcinoma Cell Line BEL-7402 Via Fas-Signaling Pathways
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Tegillarca granosa Extract Haishengsu Induces Apoptosis in Human Hepatocellular Carcinoma Cell Line BEL-7402 Via Fas-Signaling Pathways

机译:Tegillarca granosa提取物海生素通过Fas信号通路诱导人肝癌细胞BEL-7402凋亡。

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摘要

This study was designed to investigate the apoptosis-inducing properties of Tegillarca granosa extract Haishengsu (HSS) in human hepatocellular carcinoma cell line BEL-7402. Proliferation inhibition of the human hepatocellular carcinoma BEL-7402 cells was determined by the MTT assay, and the cell viability was determined by trypan blue dye exclusion assay. Apoptosis of BEL-7402 cells was demonstrated by fluorescence microscope with flow cytometry with Annexin V-FITC/PI double staining and Hoechst 33258 staining. Western blot analysis and RT-PCR were used to determine the expression levels of Fas. Expressions of caspase-8 and caspase-3 were examined by caspase activity assay and western blot analysis. HSS inhibited the proliferation of human hepatocellular carcinoma BEL-7402 cells in a dose- and time-dependent manner. Our results showed HSS had positive effect on apoptosis through flow cytometry assay and fluorescence microscope. The expressions of Fas protein and mRNA were up-regulated following the treatment. Caspase-8 and caspase-3 were activated in the cells cultured with HSS. In conclusion, HSS induced apoptosis of human hepatocellular carcinoma BEL-7402 cells. The apoptosis was associated with the up-regulation of Fas and the activations of caspase-8 and caspase-3.
机译:本研究旨在研究Tegillarca granosa提取物海生素(HSS)在人肝癌细胞BEL-7402中的凋亡诱导特性。通过MTT测定法测定人肝癌BEL-7402细胞的增殖抑制作用,通过台盼蓝染料排除测定法测定细胞活力。通过流式细胞术,膜联蛋白V-FITC / PI双重染色和Hoechst 33258染色的荧光显微镜证实BEL-7402细胞的凋亡。用蛋白质印迹分析和RT-PCR确定Fas的表达水平。通过胱天蛋白酶活性测定和蛋白质印迹分析检查胱天蛋白酶8和胱天蛋白酶3的表达。 HSS以剂量和时间依赖性的方式抑制人肝癌BEL-7402细胞的增殖。我们的结果表明,HSS通过流式细胞仪和荧光显微镜对细胞凋亡具有积极作用。处理后,Fas蛋白和mRNA的表达上调。在用HSS培养的细胞中激活了Caspase-8和Caspase-3。总之,HSS诱导人肝癌BEL-7402细胞凋亡。凋亡与Fas的上调以及caspase-8和caspase-3的激活有关。

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