4.5 Article

Gene-Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci

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CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
卷 23, 期 9, 页码 1824-1833

出版社

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1055-9965.EPI-14-0062

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资金

  1. National Cancer Institute, NIH, U.S. Department of Health and Human Services [U01 CA137088, R01 CA059045]
  2. NIH [R01 CA60987, CA-95-011, R01 CA48998, P01 CA 055075, UM1 CA167552, R01 137178, P50 CA 127003, R37 CA54281, P01 CA033619, R01 CA63464, U01 CA074783, U01 HG004446, GEI U01 HG 004438, R01 CA076366]
  3. National Cancer Institute, NIH [U01 CA122839, R25CA94880, T32CA009001]
  4. NIH: Australasian Colorectal Cancer Family Registry [U01 CA097735]
  5. Ontario Registry for Studies of Familial Colorectal Cancer [U01 CA074783]
  6. Seattle Colorectal Cancer Family Registry [U01 CA074794]
  7. German Research Council (Deutsche Forschungsgemeinschaft) [BR 1704/6-1, BR 1704/6-3, BR 1704/6-4, CH 117/1-1]
  8. German Federal Ministry of Education and Research [01KH0404, 01ER0814]
  9. NHS by the NIH [P50 CA 127003, R01 CA137178, P01 CA 087969]
  10. PHS by the NIH [CA42182]
  11. Ontario Research Fund
  12. Canadian Institutes of Health Research
  13. Ontario Institute for Cancer Research
  14. Ontario Ministry of Research and Innovation
  15. Intramural Research Program of the Division of Cancer Epidemiology and Genetics
  16. Division of Cancer Prevention
  17. National Cancer Institute
  18. DHHS
  19. Genes
  20. Environment and Health Initiative (GEI) [Z01 CP 010200]
  21. NIH from the National Cancer Institute and Office of Dietary Supplements
  22. National Heart, Lung, and Blood Institute, NIH, U.S. Department of Health and Human Services [HHSN268201100046C, HHSN268201100001C, HHSN268201100002C, HHSN268201100003C, HHSN268201100004C, HHSN271201100004C]
  23. ACS
  24. GECCO [R01 CA059045]

向作者/读者索取更多资源

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.

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