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首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Induction of Cytotoxicity and Apoptosis in Human Gastric Cancer Cell SGC-7901 by Isovaltrate Acetoxyhydrin Isolated from Patrinia heterophylla Bunge Involves a Mitochondrial Pathway and G2/M Phase Cell Cycle Arrest
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Induction of Cytotoxicity and Apoptosis in Human Gastric Cancer Cell SGC-7901 by Isovaltrate Acetoxyhydrin Isolated from Patrinia heterophylla Bunge Involves a Mitochondrial Pathway and G2/M Phase Cell Cycle Arrest

机译:诱导来自Patrinia heterophylla Bunge的脱钙乙酰氧酰苯丙嗪的人胃癌细胞SGC-7901中的细胞毒性和凋亡涉及线粒体途径和G2 / M期细胞周期滞留

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Background: Our previous study demonstrated cytotoxicity of a crude extract from Patrinia heterophylla Bunge (PHEB). In the present study, we aimed to investigate the effects of isovaltrate acetoxyhydrin (IA) isolated from PHEB on the gastric cancer cell SGC-7901, in order to explore a potential treatment for gastric cancer. Methods: MTT assays were employed to determine the effects of IA on cell vitality and proliferation, with monitoring of cell morphology changes and examination of apoptosis with Annexin V-PI staining. Flow cytometry was used to assess cell cycle progression and mitochondrial membrane potential. The activity of caspase 3, 9 was evaluated by spectrophotometry, and the protein levels of Bax, Bcl2 and Cyclin B1 were analyzed with Western blotting of total proteins extracted from cultured cells. Results: The results demonstrated direct toxicity of IA towards SGC-7901 cells. Evidence of apoptosis included blebbing and chromatin condensation. Annexin V-PI assays revealed early apoptosis, involving rapid depolarization of mitochondrial membranes and activity of caspase 3, 9 signaling pathways. Western blotting showed that Bcl2 and Bax proteins was down- and up-regulated, respectively, and cyclin B1 was up-regulated. Cell cycle analysis further indicated that IA could induce G2/M phase arrest in SGC-7901 cells. Conclusions: In conclusion, we believe that IA induces apoptosis of SGC-7901 cells, therefore providing a potential therapeutic agent for treatment of gastric cancer.
机译:背景:我们以前的研究表明来自Patrinia heterophylla Bunge(Pheb)的粗提物的细胞毒性。在本研究中,我们旨在探讨患有胃癌细胞SGC-7901上Pheb中的异戊酸乙酰氧基氢苯胺(Ia)的作用,以探讨胃癌的潜在治疗方法。方法:采用MTT测定法测定IA对细胞活力和增殖的影响,监测细胞形态变化和吞咽V-PI染色的凋亡检查。流式细胞术用于评估细胞周期进展和线粒体膜电位。通过分光光度法评价Caspase 3,9的活性,并分析Bax,Bcl2和细胞周期蛋白B1的蛋白质水平,并用从培养的细胞中提取的总蛋白质的蛋白质印迹进行分析。结果:结果表明IA对SGC-7901细胞的直接毒性。细胞凋亡的证据包括Blebbing和染色质缩合。膜蛋白V-PI测定显示出早期凋亡,涉及线粒体膜的快速去极化,Caspase 3,9信号传导途径的活性。 Western印迹显示,BCl2和Bax蛋白分别分别下调,并对细胞周期蛋白B1进行上调。细胞循环分析进一步表明IA可以在SGC-7901细胞中诱导G2 / M期捕获。结论:总之,我们认为IA诱导SGC-7901细胞的凋亡,从而提供潜在的治疗剂用于治疗胃癌。

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