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抑制人乳腺癌细胞中儿茶酚-O-甲基转移酶的活性增强了绿茶多酚(-)-EGCG 的生物学效应。

Inhibition of catechol-Omicron-methyltransferase activity in human breast cancer cells enhances the biological effect of the green tea polyphenol (-)-EGCG.

机构信息

Department of Pathology, Barbara Ann Karmanos Cancer Institute, School of Medicine, Wayne State University, Detroit, MI 48201, USA.

出版信息

Oncol Rep. 2010 Aug;24(2):563-9. doi: 10.3892/or_00000893.

Abstract

Tea is one of the most popular beverages in the world and has been studied extensively as a health-promoting beverage that may act to prevent a number of chronic diseases and cancers. (-)-Epigallocatechin gallate [(-)-EGCG], a major component in green tea, is unstable under physiological conditions and methylation of (-)-EGCG by catechol-Omicron-methyltransferase (COMT) is a modification that reduces the biological activity of (-)-EGCG. In the current study, we hypothesized that suppression of COMT activity in human breast cancer cells could increase the proteasome-inhibitory potency of (-)-EGCG and therefore enhance its tumor cell growth-inhibitory activity. We first determined the COMT genotype and basal levels of COMT activity in various human breast cancer cell lines. Furthermore, when breast cancer MDA-MB-231 cells containing high COMT activity were tested, the diminished COMT activity apparently increased the effectiveness of (-)-EGCG via augmented proteasome inhibition and apoptosis induction. This study supplements the previous findings that methylated (-)-EGCG is less bioactive and supports the notion that COMT inhibition may increase the anti-cancer properties of tea polyphenols and the combination may serve as a novel approach or supplemental treatment for breast cancer chemotherapy.

摘要

茶是世界上最受欢迎的饮料之一,作为一种促进健康的饮料,它已经被广泛研究,可能有助于预防多种慢性疾病和癌症。(-)-表没食子儿茶素没食子酸酯[(-)-EGCG]是绿茶的主要成分之一,在生理条件下不稳定,儿茶酚-O-甲基转移酶(COMT)对(-)-EGCG 的甲基化是一种降低(-)-EGCG 生物活性的修饰。在本研究中,我们假设抑制人乳腺癌细胞中的 COMT 活性可以增加(-)-EGCG 的蛋白酶体抑制效力,从而增强其肿瘤细胞生长抑制活性。我们首先确定了各种人乳腺癌细胞系中的 COMT 基因型和基础 COMT 活性。此外,当含有高 COMT 活性的乳腺癌 MDA-MB-231 细胞进行测试时,明显减少的 COMT 活性通过增强蛋白酶体抑制和诱导细胞凋亡,明显提高了(-)-EGCG 的有效性。本研究补充了先前关于甲基化(-)-EGCG 生物活性较低的发现,并支持了 COMT 抑制可能增加茶多酚抗癌特性的观点,这种联合可能成为乳腺癌化疗的一种新方法或辅助治疗。

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