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砷暴露与表观遗传改变:基于 Illumina 450K DNA 甲基化芯片的最新发现。

Arsenic Exposure and Epigenetic Alterations: Recent Findings Based on the Illumina 450K DNA Methylation Array.

机构信息

Division of Epidemiology and Biostatistics, School of Public Health, University of Illinois at Chicago, 1603 West Taylor Street, MC923, Chicago, IL, 60612, USA,

出版信息

Curr Environ Health Rep. 2015 Jun;2(2):137-44. doi: 10.1007/s40572-015-0052-1.

Abstract

Arsenic is a major public health concern worldwide. While it is an established carcinogen and associated with a number of other adverse health outcomes, the molecular mechanisms underlying arsenic toxicity are not completely clarified. There is mounting evidence from human studies suggesting that arsenic exposure is associated with epigenetic alterations, including DNA methylation. In this review, we summarize several recent human studies that have evaluated arsenic exposure using the Illumina HumanMethylation 450K BeadChip, which interrogates more than 485,000 methylation sites across the genome. Many of these studies have observed novel regions of the genome associated with arsenic exposure. However, few studies have evaluated the biological and functional relevance of these DNA methylation changes, which are still needed. We emphasize the need for future studies to replicate the identified DNA methylation signals as well as assess whether these markers are associated with risk of arsenic-related diseases.

摘要

砷是全球主要的公共卫生关注点。虽然它是一种已确定的致癌物质,并与许多其他不良健康后果有关,但砷毒性的分子机制尚未完全阐明。越来越多的来自人类研究的证据表明,砷暴露与表观遗传改变有关,包括 DNA 甲基化。在这篇综述中,我们总结了几项最近的人类研究,这些研究使用了 Illumina HumanMethylation 450K BeadChip 来评估砷暴露,该芯片检测了基因组中超过 485000 个甲基化位点。其中许多研究观察到了与砷暴露相关的基因组新区域。然而,很少有研究评估这些 DNA 甲基化变化的生物学和功能相关性,这仍然是必要的。我们强调需要未来的研究来复制已确定的 DNA 甲基化信号,并评估这些标记是否与砷相关疾病的风险相关。

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