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大豆植物雌激素与17β-雌二醇对前列腺癌细胞系中一组24个基因DNA甲基化的比较作用。

Comparative effects of soy phytoestrogens and 17β-estradiol on DNA methylation of a panel of 24 genes in prostate cancer cell lines.

作者信息

Adjakly Mawussi, Ngollo Marjolaine, Lebert André, Dagdemir Aslihan, Penault-Llorca Frédérique, Boiteux Jean-Paul, Bignon Yves-Jean, Guy Laurent, Bernard-Gallon Dominique

机构信息

a Centre Jean Perrin, Department of Oncogenetics, CBRV, Clermont-Ferrand, France and ERTICA, EA 4677 , University of Auvergne , Clermont-Ferrand , France.

出版信息

Nutr Cancer. 2014;66(3):474-82. doi: 10.1080/01635581.2014.884236. Epub 2014 Mar 18.

Abstract

Major phytoestrogens genistein and daidzein have been reported to have the ability to reverse DNA methylation in cancer cell lines. The mechanism by which genistein and daidzein have an inhibiting action on DNA methylation is not well understood. The aim of this study was to investigate the effects of soy phytoestrogens and the natural estrogen 17β-estradiol (E2) to determine whether one of the estrogen receptors is mobilized for the action of these compounds on DNA methylation. We also made a comparative study with a DNA methylation inhibitor (5-azacytidine) and a DNA methylation activator (budesonide). Three prostate cell lines, PC-3, DU-145, and LNCaP, were treated with 40 μM genistein, 110 μM daidzein, 2 μM budesonide, 2 μM 5-azacytidine, and 10 μM E2. In these 3 human prostate cancer cell lines, we performed methylation quantification using methyl-profiler-DNA-methylation analysis. Soy phytoestrogens and E2 induced a demethylation of all the promoter regions studied except for those that were unmethylated in control cells. Our results showed that E2 induces, like soy phytoestrogen, a decrease in DNA methylation in prostate cancer cell lines. This action may be mediated through ERβ.

摘要

据报道,主要的植物雌激素染料木黄酮和大豆苷元能够使癌细胞系中的DNA甲基化发生逆转。染料木黄酮和大豆苷元对DNA甲基化产生抑制作用的机制尚未完全明确。本研究的目的是调查大豆植物雌激素和天然雌激素17β-雌二醇(E2)的作用,以确定这些化合物对DNA甲基化的作用是否通过其中一种雌激素受体介导。我们还与DNA甲基化抑制剂(5-氮杂胞苷)和DNA甲基化激活剂(布地奈德)进行了对比研究。用40μM染料木黄酮、110μM大豆苷元、2μM布地奈德、2μM 5-氮杂胞苷和10μM E2处理三种前列腺癌细胞系PC-3、DU-145和LNCaP。在这三种人类前列腺癌细胞系中,我们使用甲基化分析器-DNA甲基化分析进行甲基化定量。大豆植物雌激素和E2诱导了所有研究的启动子区域的去甲基化,对照细胞中未甲基化的区域除外。我们的结果表明,E2与大豆植物雌激素一样,能诱导前列腺癌细胞系中DNA甲基化的降低。这种作用可能是通过ERβ介导的。

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