Singh Sher, Li Steven Shoei-Lung
Department of Life Science, College of Science, National Taiwan Normal University, Taipei 116, Taiwan.
Graduate Institute of Clinical Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Int J Mol Sci. 2012;13(8):10143-10153. doi: 10.3390/ijms130810143. Epub 2012 Aug 15.
The epigenetic effects on DNA methylation, histone modification, and expression of non-coding RNAs (including microRNAs) of environmental chemicals such as bisphenol A (BPA) and phthalates have expanded our understanding of the etiology of human complex diseases such as cancers and diabetes. Multiple lines of evidence from in vitro and in vivo models have established that epigenetic modifications caused by in utero exposure to environmental toxicants can induce alterations in gene expression that may persist throughout life. Epigenetics is an important mechanism in the ability of environmental chemicals to influence health and disease, and BPA and phthalates are epigenetically toxic. The epigenetic effect of BPA was clearly demonstrated in viable yellow mice by decreasing CpG methylation upstream of the Agouti gene, and the hypomethylating effect of BPA was prevented by maternal dietary supplementation with a methyl donor like folic acid or the phytoestrogen genistein. Histone H3 was found to be trimethylated at lysine 27 by BPA effect on EZH2 in a human breast cancer cell line and mice. BPA exposure of human placental cell lines has been shown to alter microRNA expression levels, and specifically, miR-146a was strongly induced by BPA treatment. In human breast cancer MCF7 cells, treatment with the phthalate BBP led to demethylation of estrogen receptor (ESR1) promoter-associated CpG islands, indicating that altered ESR1 mRNA expression by BBP is due to aberrant DNA methylation. Maternal exposure to phthalate DEHP was also shown to increase DNA methylation and expression levels of DNA methyltransferases in mouse testis. Further, some epigenetic effects of BPA and phthalates in female rats were found to be transgenerational. Finally, the available new technologies for global analysis of epigenetic alterations will provide insight into the extent and patterns of alterations between human normal and diseased tissues. In vitro models such as human embryonic stem cells may be extremely useful in bettering the understanding of epigenetic effects on human development, health and disease, because the formation of embryoid bodies in vitro is very similar to the early stage of embryogenesis.
双酚A(BPA)和邻苯二甲酸盐等环境化学物质对DNA甲基化、组蛋白修饰以及非编码RNA(包括微小RNA)表达的表观遗传效应,拓展了我们对癌症和糖尿病等人类复杂疾病病因的认识。来自体外和体内模型的多条证据表明,子宫内暴露于环境毒物所引起的表观遗传修饰可诱导基因表达改变,而这种改变可能会持续一生。表观遗传学是环境化学物质影响健康和疾病的重要机制,BPA和邻苯二甲酸盐具有表观遗传毒性。BPA对可存活的黄色小鼠的表观遗传效应通过降低刺鼠基因上游的CpG甲基化得以明确证实,而母体饮食中补充叶酸或植物雌激素染料木黄酮等甲基供体可预防BPA的低甲基化效应。在人乳腺癌细胞系和小鼠中,发现BPA通过对EZH2的作用使组蛋白H3在赖氨酸27处发生三甲基化。已表明人胎盘细胞系暴露于BPA会改变微小RNA表达水平,具体而言,BPA处理可强烈诱导miR-146a表达。在人乳腺癌MCF7细胞中,用邻苯二甲酸酯BBP处理导致雌激素受体(ESR1)启动子相关的CpG岛去甲基化,这表明BBP改变ESR1 mRNA表达是由于异常的DNA甲基化。还表明母体暴露于邻苯二甲酸酯DEHP会增加小鼠睾丸中DNA甲基化和DNA甲基转移酶的表达水平。此外,发现BPA和邻苯二甲酸盐对雌性大鼠的一些表观遗传效应具有跨代性。最后,现有的用于表观遗传改变全局分析的新技术将有助于深入了解人类正常组织与患病组织之间改变的程度和模式。诸如人类胚胎干细胞之类的体外模型对于更好地理解表观遗传学对人类发育、健康和疾病的影响可能极其有用,因为体外胚状体的形成与胚胎发生的早期阶段非常相似。