Alcohol and DNA Methylation: An Epigenome-Wide Association Study in Blood and Normal Breast Tissue

被引:39
|
作者
Wilson, Lauren E. [1 ,2 ]
Xu, Zongli [1 ]
Harlid, Sophia [1 ,3 ]
White, Alexandra J. [1 ]
Troester, Melissa A. [4 ]
Sandler, Dale P. [1 ]
Taylor, Jack A. [1 ]
机构
[1] NIEHS, Epidemiol Branch, Res Triangle Pk, NC 27709 USA
[2] Duke Univ, Sch Med, Dept Populat Hlth Sci, Durham, NC USA
[3] Umea Univ, Dept Radiat Sci, Oncol, Umea, Sweden
[4] Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC 27515 USA
基金
美国国家卫生研究院;
关键词
alcohol consumption; breast cancer; DNA methylation; epigenome-wide association study; PHOSPHOGLYCERATE DEHYDROGENASE; GLUTAMINE UPTAKE; POOR-PROGNOSIS; HIGH EXPRESSION; CANCER RISK; CELL-GROWTH; CONSUMPTION; PHGDH; SLC1A5; PROLIFERATION;
D O I
10.1093/aje/kwz032
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The biological mechanisms driving associations between alcohol consumption and chronic diseases might include epigenetic modification of DNA methylation. We explored the hypothesis that alcohol consumption is associated with methylation in an epigenome-wide association study of blood and normal breast tissue DNA. Infinium HumanMethylation450 BeadChip (Illumina Inc., San Diego, California) array data on blood DNA methylation was examined in a discovery set of 2,878 non-Hispanic white women from the Sister Study (United States, 2004-2015) who provided detailed questionnaire information on lifetime alcohol use. Robust linear regression modeling was used to identify significant associations (false discovery rate of Q < 0.05) between the number of alcoholic drinks per week and DNA methylation at 5,458 cytosine-phosphate-guanine (CpG) sites. Associations were replicated (P < 0.05) for 677 CpGs in an independent set of 187 blood DNA samples from the Sister Study and for 628 CpGs in an independent set of 171 normal breast DNA samples; 1,207 CpGs were replicated in either blood or normal breast, with 98 CpGs replicated in both tissues. Individual gene effects were notable for phosphoglycerate dehydrogenase (PGHDH), peptidyl-prolyl cis-trans isomerase (PPIF), solute carrier 15 (SLC15), solute carrier family 43 member 1 (SLC43A1), and solute carrier family 7 member 11 (SLC7A11). We also found that high alcohol consumption was associated with significantly lower global methylation as measured by the average of CpGs on the entire array.
引用
收藏
页码:1055 / 1065
页数:11
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