Suppr超能文献

茶多酚对人癌细胞系生长的抑制及凋亡诱导作用

Inhibition of growth and induction of apoptosis in human cancer cell lines by tea polyphenols.

作者信息

Yang G Y, Liao J, Kim K, Yurkow E J, Yang C S

机构信息

Laboratory for Cancer Research, College of Pharmacy, Rutgers University, Piscataway, NJ 08855-0789, USA.

出版信息

Carcinogenesis. 1998 Apr;19(4):611-6. doi: 10.1093/carcin/19.4.611.

Abstract

In order to study the biological activities of tea preparations and purified tea polyphenols, their growth inhibitory effects were investigated using four human cancer cell lines. Growth inhibition was measured by [3H]thymidine incorporation after 48 h of treatment. The green tea catechins (-)-epigallocatechin-3-gallate (EGCG) and (-)-epigallocatechin (EGC) displayed strong growth inhibitory effects against lung tumor cell lines H661 and H1299, with estimated IC50 values of 22 microM, but were less effective against lung cancer cell line H441 and colon cancer cell line HT-29 with IC50 values 2- to 3-fold higher. (-)-Epicatechin-3-gallate, had lower activities, and (-)-epicatechin was even less effective. Preparations of green tea polyphenols and theaflavins had higher activities than extracts of green tea and decaffeinated green tea. The results suggest that the growth inhibitory activity of tea extracts is caused by the activities of different tea polyphenols. Exposure of H661 cells to 30 microM EGCG, EGC or theaflavins for 24 h led to the induction of apoptosis as determined by an annexin V apoptosis assay, showing apoptosis indices of 23, 26 and 8%, respectively; with 100 microM of these compounds, the apoptosis indices were 82, 76 and 78%, respectively. Incubation of H661 cells with EGCG also induced a dose-dependent formation of H2O2. Addition of H2O2 to H661 cells caused apoptosis in a manner similar to that caused by EGCG. The EGCG-induced apoptosis in H661 cells was completely inhibited by exogenously added catalase (50 units/ml). These results suggest that tea polyphenol-induced production of H2O2 may mediate apoptosis and that this may contribute to the growth inhibitory activities of tea polyphenols in vitro.

摘要

为了研究茶制剂和纯化茶多酚的生物活性,使用四种人类癌细胞系研究了它们的生长抑制作用。处理48小时后,通过[3H]胸苷掺入法测量生长抑制情况。绿茶儿茶素(-)-表没食子儿茶素-3-没食子酸酯(EGCG)和(-)-表没食子儿茶素(EGC)对肺癌细胞系H661和H1299表现出强烈的生长抑制作用,估计IC50值为22 microM,但对肺癌细胞系H441和结肠癌细胞系HT-29效果较差,IC50值高2至3倍。(-)-表儿茶素-3-没食子酸酯活性较低,(-)-表儿茶素效果更差。绿茶多酚和茶黄素制剂的活性高于绿茶提取物和脱咖啡因绿茶提取物。结果表明,茶提取物的生长抑制活性是由不同茶多酚的活性引起的。用30 microM的EGCG、EGC或茶黄素处理H661细胞24小时,通过膜联蛋白V凋亡检测法测定,导致细胞凋亡的诱导,凋亡指数分别为23%、26%和8%;使用100 microM的这些化合物时,凋亡指数分别为82%、76%和78%。用EGCG孵育H661细胞也诱导了剂量依赖性的H2O2形成。向H661细胞中添加H2O2以类似于EGCG引起细胞凋亡的方式导致细胞凋亡。外源性添加过氧化氢酶(50单位/毫升)可完全抑制EGCG诱导的H661细胞凋亡。这些结果表明,茶多酚诱导产生H2O2可能介导细胞凋亡,这可能有助于茶多酚在体外的生长抑制活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验