Gene-Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci

被引:42
|
作者
Kantor, Elizabeth D. [1 ,2 ,3 ]
Hutter, Carolyn M. [4 ]
Minnier, Jessica [2 ,5 ]
Berndt, Sonja I. [6 ]
Brenner, Hermann [7 ,8 ]
Caan, Bette J. [9 ]
Campbell, Peter T. [10 ]
Carlson, Christopher S. [2 ,3 ]
Casey, Graham [11 ]
Chan, Andrew T. [12 ,13 ,14 ]
Chang-Claude, Jenny [15 ]
Chanock, Stephen J. [6 ]
Cotterchio, Michelle [16 ]
Du, Mengmeng [2 ,3 ,13 ,14 ]
Duggan, David [17 ]
Fuchs, Charles S. [13 ,14 ,18 ]
Giovannucci, Edward L. [19 ]
Gong, Jian [2 ]
Harrison, Tabitha A. [2 ]
Hayes, Richard B. [20 ]
Henderson, Brian E. [21 ]
Hoffmeister, Michael [7 ]
Hopper, John L. [22 ]
Jenkins, Mark A. [22 ]
Jiao, Shuo [2 ]
Kolonel, Laurence N. [23 ]
Le Marchand, Loic [23 ]
Lemire, Mathieu [24 ]
Ma, Jing [13 ,14 ]
Newcomb, Polly A. [2 ,3 ]
Ochs-Balcom, Heather M. [25 ]
Pflugeisen, Bethann M. [2 ]
Potter, John D. [2 ,3 ,26 ]
Rudolph, Anja [27 ]
Schoen, Robert E. [28 ]
Seminara, Daniela [4 ]
Slattery, Martha L. [29 ]
Stelling, Deanna L. [2 ]
Thomas, Fridtjof [30 ]
Thornquist, Mark [2 ]
Ulrich, Cornelia M. [2 ,3 ,31 ,32 ]
Warnick, Greg S. [2 ]
Zanke, Brent W. [33 ]
Peters, Ulrike [2 ,3 ]
Hsu, Li [2 ,34 ]
White, Emily [2 ,3 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA
[3] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98195 USA
[4] NCI, Div Canc Control & Populat Sci, NIH, Bethesda, MD 20892 USA
[5] Oregon Hlth & Sci Univ, Dept Publ Hlth & Prevent Med, Portland, OR 97201 USA
[6] NCI, Div Canc Epidemiol & Genet, NIH, Bethesda, MD 20892 USA
[7] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Heidelberg, Germany
[8] German Canc Consortium DKTK, Heidelberg, Germany
[9] Kaiser Permanente Med Care Program, Div Res, Oakland, CA 94611 USA
[10] Amer Canc Soc, Epidemiol Res Program, Atlanta, GA 30329 USA
[11] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA 90033 USA
[12] Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA 02114 USA
[13] Harvard Univ, Sch Med, Boston, MA USA
[14] Brigham & Womens Hosp, Channing Div Network Med, Boston, MA 02115 USA
[15] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany
[16] Canc Care Ontario, Toronto, ON, Canada
[17] Translat Genom Res Inst, Phoenix, AZ USA
[18] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[19] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[20] NYU, Sch Med, Dept Populat Hlth, Div Epidemiol, New York, NY USA
[21] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[22] Univ Melbourne, Melbourne Sch Populat Hlth, Melbourne, Vic 3010, Australia
[23] Univ Hawaii, Ctr Canc, Program Epidemiol, Honolulu, HI 96822 USA
[24] Ontario Inst Canc Res, Toronto, ON, Canada
[25] SUNY Buffalo, Dept Social & Prevent Med, Buffalo, NY 14260 USA
[26] Massey Univ, Ctr Publ Hlth Res, Wellington, New Zealand
[27] German Canc Res Ctr, Unit Genet Epidemiol, Div Canc Epidemiol, Heidelberg, Germany
[28] Univ Pittsburgh, Med Ctr, Dept Med & Epidemiol, Pittsburgh, PA USA
[29] Univ Utah, Hlth Sci Ctr, Dept Internal Med, Salt Lake City, UT USA
[30] Univ Tennessee, Hlth Sci Ctr, Dept Prevent Med, Memphis, TN USA
[31] Natl Ctr Tumor Dis, Div Prevent Oncol, Heidelberg, Germany
[32] German Canc Res Ctr, Heidelberg, Germany
[33] Ottawa Hosp, Res Inst, Clin Epidemiol Program, Ottawa, ON, Canada
[34] Univ Washington, Sch Publ Hlth, Dept Biostat, Seattle, WA 98195 USA
基金
加拿大健康研究院;
关键词
GENOME-WIDE ASSOCIATION; DOSE-RESPONSE METAANALYSIS; RISK LOCUS; VARIANTS; SCAN; BIAS; 1Q41; 8Q24;
D O I
10.1158/1055-9965.EPI-14-0062
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Genome-wide association studies have identified several single nucleotide polymorphisms (SNPs) that are associated with risk of colorectal cancer. Prior research has evaluated the presence of gene-environment interaction involving the first 10 identified susceptibility loci, but little work has been conducted on interaction involving SNPs at recently identified susceptibility loci, including: rs10911251, rs6691170, rs6687758, rs11903757, rs10936599, rs647161, rs1321311, rs719725, rs1665650, rs3824999, rs7136702, rs11169552, rs59336, rs3217810, rs4925386, and rs2423279. Methods: Data on 9,160 cases and 9,280 controls from the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) and Colon Cancer Family Registry (CCFR) were used to evaluate the presence of interaction involving the above-listed SNPs and sex, body mass index (BMI), alcohol consumption, smoking, aspirin use, postmenopausal hormone (PMH) use, as well as intake of dietary calcium, dietary fiber, dietary folate, red meat, processed meat, fruit, and vegetables. Interaction was evaluated using a fixed effects meta-analysis of an efficient Empirical Bayes estimator, and permutation was used to account for multiple comparisons. Results: None of the permutation-adjusted P values reached statistical significance. Conclusions: The associations between recently identified genetic susceptibility loci and colorectal cancer are not strongly modified by sex, BMI, alcohol, smoking, aspirin, PMH use, and various dietary factors. Impact: Results suggest no evidence of strong gene-environment interactions involving the recently identified 16 susceptibility loci for colorectal cancer taken one at a time. (C) 2014 AACR.
引用
收藏
页码:1824 / 1833
页数:10
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