Epigenetic Targets of Arsenic: Emphasis on Epigenetic Modifications During Carcinogenesis

被引:23
作者
Roy, Ram Vinod
Son, Young-Ok
Pratheeshkumar, Poyil
Wang, Lei
Hitron, John Andrew
Divya, Sasidharan Padmaja
Rakesh, D.
Kim, Donghern
Yin, Yuanqin
Zhang, Zhuo
Shi, Xianglin [1 ]
机构
[1] Univ Kentucky, Ctr Res Environm Dis, Lexington, KY 40536 USA
基金
美国国家卫生研究院;
关键词
epigenetics; DNA methylation; histone modification; chromatin; miRNAs; transgenerational; intergeneration; arsenic; carcinogenesis; epigenome; prenatal exposure; INDUCED MALIGNANT-TRANSFORMATION; ENDOCRINE DISRUPTOR VINCLOZOLIN; DE-NOVO METHYLATION; DNA METHYLATION; DRINKING-WATER; GENE-EXPRESSION; TRANSGENERATIONAL ACTIONS; HISTONE MODIFICATIONS; TRANSCRIPTION FACTOR; DOWN-REGULATION;
D O I
10.1615/JEnvironPatholToxicolOncol.2014012066
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
DNA methylation and histone modification promote opening and closure of chromatin structure, which affects gene expression without altering the DNA sequence. Epigenetic markers regulate the dynamic nature of chromatin structure at different levels: DNA, histone, noncoding RNAs, as well as the higher-order chromatin structure. Accumulating evidence strongly suggests that arsenic-induced carcinogenesis involves frequent changes in the epigenetic marker. However, progress in identifying arsenic-induced epigenetic changes has already been made using genome-wide approaches; the biological significance of these epigenetic changes remains unknown. Moreover, arsenic-induced changes in the chromatin state alter gene expression through the epigenetic mechanism. The current review provides a summary of recent literature regarding epigenetic changes caused by arsenic in carcinogenesis. We highlight the transgenerational studies needed to explicate the biological significance and toxicity of arsenic over a broad spectrum.
引用
收藏
页码:63 / 84
页数:22
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