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THE EFFECT OF EXPOSURE TO CARCINOGENIC METALS ON HISTONE TAIL MODIFICATIONS AND GENE EXPRESSION IN HUMAN SUBJECTS

机译:致癌物质暴露于人体受试者组蛋白尾改性和基因表达的影响

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摘要

The precise mechanisms for the carcinogenesis of nickel and arsenic compounds are not completely understood. In recent years, alterations of epigenetic mechanisms have been implicated in the carcinogenesis of these two metal compounds. In vitro exposure to nickel or arsenic induces changes in both DNA methylation patterns, as well as, in the levels of posttranslational modifications of histone tails. Changes in DNA methylation patterns have been reported in human subjects exposed to arsenic. Here we review our recent reports on the alterations in global levels of posttranslational histone modifications in peripheral blood mononuclear cells (PBMCs) of subjects with occupational exposure to nickel and subjects exposed to arsenic in their drinking water. Occupational exposure to nickel was associated with an increase in H3K4me3 and decrease in H3K9me2. A global increase in H3K9me2 and decrease in H3K9ac was found in subjects exposed to arsenic. Additionally, exposure to arsenic resulted in opposite changes in a number of histone modifications in males compared to females. The results of these two studies suggest that exposure to nickel or arsenic compounds, and possibly other carcinogenic metal compounds, can induce changes in global levels of posttranslational histone modifications in peripheral blood mononuclear cells.
机译:不完全理解镍和砷化合物的致癌物的精确机制。近年来,表观遗传机制的改变涉及这两个金属化合物的致癌作用。体外暴露于镍或砷,诱导DNA甲基化模式的变化,以及在组蛋白尾部的后期改变后的水平中。在暴露于砷的人受试者中报道了DNA甲基化模式的变化。在这里,我们审查了我们最近关于在其饮用水中暴露于砷的镍和受试者的受试者外周血单核细胞(PBMC)在外周血单核细胞(PBMC)中的全球后期血液单核细胞(PBMC)的改变的报告。职业暴露于镍与H3K4ME3的增加和H3K9ME2的增加有关。在暴露于砷的受试者中发现了H3K9ME2的全局增加和H3K9Ac的降低。另外,与女性相比,暴露于砷导致雄性中许多组蛋白修饰的相反变化。这两项研究的结果表明,暴露于镍或砷化合物,以及可能的其他致癌金属化合物,可以诱导外周血单核细胞中的全球性组蛋白修饰的全球水平的变化。

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