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姜黄素通过 MAPK 通路诱导 MDA-MB-435 人乳腺癌细胞中 EZH2 的下调表达。

Curcumin induces down-regulation of EZH2 expression through the MAPK pathway in MDA-MB-435 human breast cancer cells.

机构信息

State Key Laboratory of Oncology in South China, Cancer Center, Sun Yat-Sen University, Guangzhou, China.

出版信息

Eur J Pharmacol. 2010 Jul 10;637(1-3):16-21. doi: 10.1016/j.ejphar.2010.03.051. Epub 2010 Apr 10.

Abstract

Curcumin, a natural compound isolated from turmeric, may inhibit cell proliferation in various tumor cells through a mechanism that is not fully understood. The enhancer of zeste homolog 2 (EZH2) gene is overexpressed in human breast cancers with poor prognosis. In this study, we observed a dose- and time-dependent down-regulation of expression of EZH2 by curcumin that correlates with decreased proliferation in the MDA-MB-435 breast cancer cell line. The curcumin treatment resulted in an accumulation of cells in the G(1) phase of the cell cycle. Further investigation revealed that curcumin-induced down-regulation of EZH2 through stimulation of three major members of the mitogen-activated protein kinase (MAPK) pathway: c-Jun NH2-terminal kinase (JNK), extracellular signal-regulated kinase (ERK) and p38 kinase. These data suggest that an underlying mechanism of the MAPK pathway mediates the down-regulation of EZH2, thus contributing to the anti-proliferative effects of curcumin against breast cancer.

摘要

姜黄素是从姜黄中分离出来的天然化合物,其可能通过尚未完全阐明的机制抑制多种肿瘤细胞的增殖。在具有不良预后的人类乳腺癌中,EZH2 基因(增强子的锌指蛋白 2)过表达。在本研究中,我们观察到姜黄素可剂量依赖性、时间依赖性地下调 EZH2 的表达,这与 MDA-MB-435 乳腺癌细胞系增殖减少相关。姜黄素处理导致细胞在细胞周期的 G1 期积累。进一步的研究表明,姜黄素通过刺激丝裂原活化蛋白激酶(MAPK)途径的三个主要成员(c-Jun NH2-末端激酶(JNK)、细胞外信号调节激酶(ERK)和 p38 激酶)诱导 EZH2 的下调。这些数据表明,MAPK 途径的潜在机制介导了 EZH2 的下调,从而有助于姜黄素对乳腺癌的抗增殖作用。

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