Association of XRCC1 polymorphisms with arsenic methylation

被引:0
|
作者
Junko Fujihara
Toshihiro Yasuda
Hisato Iwata
Shinsuke Tanabe
Haruo Takeshita
机构
[1] Shimane University School of Medicine,Department of Legal Medicine
[2] University of Fukui,Division of Medical Genetics and Biochemistry, Faculty of Medical Sciences
[3] Ehime University,Center for Marine Environmental Studies (CMES)
来源
Archives of Toxicology | 2016年 / 90卷
关键词
X-ray repair cross-complementing group 1 (XRCC1); Base excision repair (BER); Single nucleotide polymorphisms (SNPs); 8-Hydroxy-2′-deoxyguanosine (8-OHdG); Arsenic compounds;
D O I
暂无
中图分类号
学科分类号
摘要
The associations of four single nucleotide polymorphisms (p.Arg194Trp, p.Arg280His, p.Pro206Pro, and p.Arg399Gln) in X-ray repair cross-complementing group 1 with urinary arsenic metabolites and 8-hydroxy-2′-deoxyguanosine (8-OHdG) were investigated in a Vietnamese population (n = 100). Individuals with genotype AA in p.Pro206Pro showed significantly higher urinary monomethylarsonic acid (MMAV) and lower dimethylarsinic acid (DMAV)/MMAV ratio than genotype AG. As for p.Arg399Gln, both Arg/Arg homozygous subjects and Arg/Gln heterozygous individuals showed a significantly higher urinary inorganic As percentage and lower 8-OHdG concentrations than Gln/Gln homozygous. Our results suggested that Arg399Gln is a functional SNP that may be related to DNA repair activity.
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页码:1009 / 1012
页数:3
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