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茶黄素-3,3'-双没食子酸酯诱导表皮生长因子受体下调。

Theaflavin-3, 3'-digallate induces epidermal growth factor receptor downregulation.

作者信息

Mizuno Hideya, Cho Yong-Yeon, Zhu Feng, Ma Wei-Ya, Bode Ann M, Yang Chung S, Ho Chi-Tang, Dong Zigang

机构信息

Hormel Institute, University of Minnesota, Austin, Minnesota 55912, USA.

出版信息

Mol Carcinog. 2006 Mar;45(3):204-12. doi: 10.1002/mc.20174.

Abstract

Black tea is one of the most popular beverages worldwide and especially in Western nations. Theaflavins, a mixture of theaflavin (TF-1), theaflavin-3-gallate (TF-2a), theaflavin-3'-gallate (TF-2b), and theaflavin-3,3'-digallate (TF-3) are the major components of black tea. Among these black tea components, theaflavin is generally considered to be the more effective component for the inhibition of carcinogenesis. Recently, TF-3 has been shown to have an antiproliferative effect on tumor cells, but the mechanism is not clear. In this study, we showed that TF-3-induced internalization and downregulation of the epidermal growth factor receptor (EGFR). These results suggested that TF-3 induces EGFR endocytosis and degradation. We further showed that TF-3 stimulated EGFR ubiquitination and tyrosine kinase activation. Interestingly, TF-3-induced EGFR downregulation is inhibited by the proteasome inhibitor, MG132, but not by the EGFR-specific receptor tyrosine kinase inhibitor, AG1478. Furthermore, pretreatment with TF-3 inhibited EGF-induced EGFR autophosphorylation, ERKs phosphorylation and AP-1 activation in JB6 Cl41 cells. In addition, TF-3 inhibited EGF-induced anchorage-independent cell transformation. Overall, our results indicate that TF-3 might exert chemopreventive effects through the downregulation of the EGFR.

摘要

红茶是全球尤其是西方国家最受欢迎的饮品之一。茶黄素是红茶的主要成分,它是由茶黄素(TF-1)、茶黄素-3-没食子酸酯(TF-2a)、茶黄素-3'-没食子酸酯(TF-2b)和茶黄素-3,3'-双没食子酸酯(TF-3)组成的混合物。在这些红茶成分中,茶黄素通常被认为是抑制致癌作用更有效的成分。最近,TF-3已被证明对肿瘤细胞具有抗增殖作用,但其机制尚不清楚。在本研究中,我们发现TF-3可诱导表皮生长因子受体(EGFR)的内化和下调。这些结果表明TF-3诱导EGFR内吞和降解。我们进一步发现TF-3刺激EGFR泛素化和酪氨酸激酶激活。有趣的是,蛋白酶体抑制剂MG132可抑制TF-3诱导的EGFR下调,但EGFR特异性受体酪氨酸激酶抑制剂AG1478则不能。此外,用TF-3预处理可抑制EGF诱导的JB6 Cl41细胞中EGFR的自磷酸化、ERK的磷酸化和AP-1的激活。此外,TF-3抑制EGF诱导的非贴壁依赖性细胞转化。总体而言,我们的结果表明TF-3可能通过下调EGFR发挥化学预防作用。

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