Arsenic and the Epigenome: Interindividual Differences in Arsenic Metabolism Related to Distinct Patterns of DNA Methylation

被引:96
作者
Bailey, Kathryn A. [1 ]
Wu, Michael C. [2 ]
Ward, William O. [3 ]
Smeester, Lisa [1 ]
Rager, Julia E. [1 ]
Garcia-Vargas, Gonzalo [4 ]
Del Razo, Luz-Maria [5 ]
Drobna, Zuzana [6 ]
Styblo, Miroslav [1 ]
Fry, Rebecca C. [1 ]
机构
[1] Univ N Carolina, Dept Environm Sci & Engn, UNC Gillings Sch Global Publ Hlth, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Biostat, UNC Gillings Sch Global Publ Hlth, Chapel Hill, NC 27599 USA
[3] US EPA, Natl Hlth & Environm Effects Res Lab, Off Res & Dev, Res Triangle Pk, NC 27711 USA
[4] Juarez Univ Durango State, Fac Med, Durango, CO, Mexico
[5] IPN, Dept Toxicol, CINVESTAV, Mexico City 07738, DF, Mexico
[6] Univ N Carolina, Dept Nutr, UNC Gillings Sch Global Publ Hlth, Chapel Hill, NC 27599 USA
关键词
Arsenic; Epigenome; DNA Methylation; Arsenic biotransformation; SIGNAL-TRANSDUCTION PATHWAYS; DOSE-RESPONSE RELATIONSHIPS; TNF RECEPTORS 1; DRINKING-WATER; INSULIN-RESISTANCE; OXIDATIVE STRESS; CHRONIC EXPOSURE; ASSOCIATION; CELLS; MECHANISMS;
D O I
10.1002/jbt.21462
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Biotransformation of inorganic arsenic (iAs) is one of the factors that determines the character and magnitude of the diverse detrimental health effects associated with chronic iAs exposure, but it is unknown how iAs biotransformation may impact the epigenome. Here, we integrated analyses of genome-wide, gene-specific promoter DNA methylation levels of peripheral blood leukocytes with urinary arsenical concentrations of subjects from a region of Mexico with high levels of iAs in drinking water. These analyses revealed dramatic differences in DNA methylation profiles associated with concentrations of specific urinary metabolites of arsenic (As). The majority of individuals in this study had positive indicators of As-related disease, namely pre-diabetes mellitus or diabetes mellitus (DM). Methylation patterns of genes with known associations with DM were associated with urinary concentrations of specific iAs metabolites. Future studies will determine whether these DNA methylation profiles provide mechanistic insight into the development of iAs-associated disease, predict disease risk, and/or serve as biomarkers of iAs exposure in humans. (c) 2012 Wiley Periodicals, Inc. J BiochemMol Toxicol 27:106-115, 2013; View this article online at wileyonlinelibrary.com. DOI 10.1002/jbt.21462
引用
收藏
页码:106 / 115
页数:10
相关论文
共 75 条
[1]
Amer Diabet Assoc, 2012, DIABETES CARE, V35, pS64, DOI [10.2337/dc19-S002, 10.2337/dc12-S064, 10.2337/dc23-S002, 10.2337/dc09-S062, 10.2337/dc18-S002]
[2]
[Anonymous], 2015, GUIDELINES DRINKING
[3]
Aronoff SL., 2004, Diabetes Spect, V17, P183, DOI DOI 10.2337/DIASPECT.17.3.183
[4]
A feat of metabolic proportions: Pdx 1 orchestrates islet development and function in the maintenance of glucose homeostasis [J].
Babu, Daniella A. ;
Deering, Tye G. ;
Mirmira, Raghavendra G. .
MOLECULAR GENETICS AND METABOLISM, 2007, 92 (1-2) :43-55
[5]
Bailey K.A., 2012, TOXICOLOGY EPIGENETI, P149
[6]
Baumgartener James W., 2003, Current Drug Targets - Immune Endocrine and Metabolic Disorders, V3, P291, DOI 10.2174/1568008033340144
[7]
TNFRSF1B in genetic predisposition to clinical neuropathy and effect on HDL cholesterol and glycosylated hemoglobin in type 2 diabetes [J].
Benjafield, AV ;
Glenn, CL ;
Wang, XL ;
Colagiuri, S ;
Morris, BJ .
DIABETES CARE, 2001, 24 (04) :753-757
[8]
CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[9]
Protein kinase Cδ participates in insulin-induced activation of PKB via PDK1 [J].
Brand, Chagit ;
Cipok, Michal ;
Attali, Veronique ;
Bak, Asia ;
Sampson, Sanford R. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 349 (03) :954-962
[10]
Deletion of protein kinase Cδ in mice modulates stability of inflammatory genes and protects against cytokine-stimulated beta cell death in vitro and in vivo [J].
Cantley, J. ;
Boslem, E. ;
Laybutt, D. R. ;
Cordery, D. V. ;
Pearson, G. ;
Carpenter, L. ;
Leitges, M. ;
Biden, T. J. .
DIABETOLOGIA, 2011, 54 (02) :380-389