期刊文献+

儿茶素单体EGCG体外诱导胃癌MGC—803细胞凋亡的研究 被引量:1

Induction of apoptosis in human gastric cancer cell line by EGCG
下载PDF
导出
摘要 目的:探讨表没食子儿茶素酸酯(Epigallatechin—3—gallate,EGCG)体外诱导胃癌MGC—803细胞凋亡作用。方法:以不同浓度EGCG分别处理MGC—803细胞,用琼脂糖凝胶电泳、荧光显微镜、MTT法观察MGC—803细胞DNA带型、形态和抑制率的变化。结果:琼脂糖凝胶电泳呈典型的DNA“梯状带”,高浓度EGCG(1×10-3M)作用33小时后DNA呈弥散的“膜状带”。荧光显微镜下可见细胞出现染色质浓缩、胞膜吐泡等凋亡现象。MTT法测定不同浓度EGCG对MGC—803细胞生长有明显抑制。结论:EGCG有明显的诱导胃癌MGC—803细胞凋亡作用,高浓度EGCG直接导致细胞坏死。 objective: To study the effect of epigallatechin-3-gallate (EGCG) on the growthand apoptosis of gastric cancer MGC-803 cell line. Methods: Changes in DNA fragment, morphol-ogy and growth inhibition rate of MGC- 803 cell line were evaluated by agrose gel eletrophoresis,fluorescent microscopy and MTT assay. Results:Apoptosis characterization of DNA laddering bandappeared in the MGC- 803 cell after treated with EGCG at 1×10-4 M or 1×10-5 M for 33 hours,but at 1×10-3M DNA fragment was smear band shaped. Condensation of chromosome and bleb-bing of the plasma membrane were found in the apoptotic cells under fluorescent microscopy. MTTassay showed growth inhibition of MGC- 803 cells induced by EGCG. Conclusion: EGCG may in-duce apoptosis of gastric cancer MGC-803 cells significantly, and high concentration EGCG maycause the necrosis of the cells directly.
出处 《武警后勤学院学报(医学版)》 CAS 1999年第4期204-206,209,共4页 Journal of Logistics University of PAP(Medical Sciences)
关键词 表没食子儿茶素酸酯 胃癌MGC—803细胞 细胞凋亡 生长抑制率 Epigallatechin-3-gallate MGC-803 cell Apoptosis Growth inhibition rate
  • 相关文献

参考文献10

二级参考文献15

共引文献223

同被引文献13

  • 1周薇,罗招阳,周秀田,宋颖,曹娟,陈科.表没食子儿茶素没食子酸酯诱导人胃癌MGC-803细胞凋亡及机制[J].中国肿瘤,2005,14(12):811-814. 被引量:14
  • 2ZHIVOTOVSKY B, ORRENIUS S. Carcinogenesis and apoptosis: paradigms and paradoxes [ J ]. Carcinogenesis, 2006, 27 ( 10 ) : 1939-1945.
  • 3HOU Z, LAMBERT J D, CHIN K V, et al. Effects of tea polyphenols on signal transduction pathways related to cancer chemoprevention[J]. Mutat Res, 2004, 555(1/2) : 3-19.
  • 4QANUGO S, DAS M, HALDAR S, et al. Epigallocatechin-3-gallate induces mitochondrial membrane depolarization and caspasedependent apoptosis in pancreatic cancer cells [ J ]. Carcinogenesis,2005, 26(5): 958-967.
  • 5NOGUCHI M, YOKOYAMA M, WATANABE S, et al. Inhibitory effect of the tea polyphenol, ( - )-epigallocatechin gallate, on growth of cervical adenocarcinoma cell lines [ J ]. Carver Lett, 2006, 234(2) : 135-142.
  • 6STUART E C, SCANDLYN M J, ROSENGREN R J. Role of epigallocatechin gallate (EGCG) in the treatment of breast and prostate cancer[ J ]. Life Sci,2006, 79 (25) : 2329-2336.
  • 7HORIE N, HIRABAYASHI N, TAKAHASHI Y, et al. Synergistic effect of green tea catechins on cell growth and apoptosis induction in gastric carcinoma cells[J].Biol Pharm Bull, 2005, 28 (4) : 574-579.
  • 8ROULSTON A, REINHARD C, AMIRI P, et al. Early activation of c-Jun N-terminal protein kinase activation and p38 kinase regulate cell survival in response to tumor necrosis factor alpha[ J ]. J Biol Chem, 1998, 273 ( 17 ) : 10232-10239.
  • 9WU GS. The functional interactions between the p53 and MAPK signaling pathways [ J ]. Cancer Biol Ther, 2004, 3 (2) : 156- 161.
  • 10MIYOSHI N, UCHIDA K, OSAWA T, et al. A link between benzyl isothiocyanate- induced cell cycle arrest and apoptosis: involvement of mitogen-activated protein kinases in the Bcl-2 phosphory-lation[J]. Cancer Res, 2004; 64(6): 2134-2142.

引证文献1

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部