...
首页> 外文期刊>Journal of digestive diseases >Effect of parthenolide on proliferation and apoptosis in gastric cancer cell line SGC7901.
【24h】

Effect of parthenolide on proliferation and apoptosis in gastric cancer cell line SGC7901.

机译:疗效对胃癌细胞系SGC7901中增殖和凋亡的影响。

获取原文
获取原文并翻译 | 示例

摘要

OBJECTIVE: To investigate the effect of parthenolide (PAR) on proliferation and apoptosis in gastric cancer cell line SGC7901. METHODS: Human gastric cancer cell line SGC7901 cells were incubated with various concentration of PAR. After various periods of incubation, the proliferation of SGC7901 cells was assessed by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide methyl thiazolyl tetrazolium (MTT) assay. Apoptosis was measured by the annexin V-fluorescein isothiocyanate fluoresceine isothiocyanate (FITC)/propidium iodide (PI) double labeled staining method and the morphology of the cell was observed under a fluorescent microscope. Mitochondrial potential was measured by flow cytometry after Rhodamine 123 staining. The expressions of cytochrome C and the Bcl-2 family of proteins, including Bcl-2, Bax, Bid and tBid were measured by Western blot. Caspase 3 and 8 activities were measured by enzyme-linked immunosorbent assay. RESULTS: Treatment with PAR induced apoptosis as confirmed by annexin V-FITC/PI assay. PAR-induced apoptosis was associated with intracellular events including the decline of mitochondrial potential, increased release of cytochrome C from the mitochondria, decreased expression of Bcl-2, increased expression of Bax, Bid and tBid and activation of caspase 3 and 8. CONCLUSION: These results suggest that possibly via activation of the mitochondrial pathway, PAR causes mitochondrial damage leading to the release of cytochrome C and by regulating the expression of the Bcl-2 family of proteins and activating caspases which leads to results in apoptotic cell death in SGC7901 cells. Our results might be helpful in formulating new therapeutic approaches using Chinese herbal medicine.
机译:目的:探讨疗法(Par)对胃癌细胞系SGC7901中增殖和细胞凋亡的影响。方法:将人胃癌细胞系SGC7901细胞与各种浓度的均培育。孵育各种时期后,通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴铵(MTT)测定评估SGC7901细胞的增殖。通过膜蛋白V-荧光素异硫氰酸酯荧光胺异硫氰酸酯(FITC)/碘化乙酸苯甲酸苯(PI)双标记染色方法和细胞的形态测量细胞凋亡,并在荧光显微镜下观察细胞的形态。通过流式细胞术在罗丹明123染色后通过流式细胞术测量线粒体电位。通过蛋白质印迹测量细胞色素C和Bcl-2蛋白质的蛋白质系列的表达,包括Bcl-2,Bax,Bid和Tbid。通过酶联免疫吸附测定法测量Caspase 3和8活性。结果:通过膜蛋白V-FITC / PI测定进行诱导细胞凋亡治疗。诱导的细胞凋亡与细胞内事件有关,包括线粒体潜力下降,从线粒体释放细胞色素C的释放,降低了Bcl-2的表达,增加了Bax,Bid和Tbid的表达和Caspase 3和8的活化。结论:这些结果表明,可能通过线粒体途径的激活,PAR导致线粒体损伤导致细胞色素C的释放,并通过调节Bcl-2蛋白的表达和激活胱天蛋白酶,这导致SGC7901细胞中的凋亡细胞死亡导致凋亡细胞死亡。我们的结果可能有助于使用中草药制定新的治疗方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号