4.6 Article

Genome-Wide Diet-Gene Interaction Analyses for Risk of Colorectal Cancer

Journal

PLOS GENETICS
Volume 10, Issue 4, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1004228

Keywords

-

Funding

  1. GECCO: National Cancer Institute, National Institutes of Health, U.S. Department of Health and Human Services [U01 CA137088, R01 CA059045, R01 CA120582]
  2. CCFR: National Institutes of Health (RFA) [CA-95-011]
  3. National Cancer Institute, National Institutes of Health [U01 CA122839]
  4. National Institutes of Health: Australasian Colorectal Cancer Family Registry [U01 CA097735]
  5. National Institutes of Health: Seattle Colorectal Cancer Family Registry [U01 CA074794]
  6. National Institutes of Health: Ontario Registry for Studies of Familial Colorectal Cancer [U01 CA074783]
  7. DACHS: 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. DALS: National Institutes of Health [R01 CA48998]
  10. National Institutes of Health [P01 CA 055075, UM1 CA167552, R01 137178, P50 CA 127003]
  11. NHS by the National Institutes of Health [R01 137178, P50 CA 127003, P01 CA 087969]
  12. OFCCR: National Institutes of Health [U01 CA074783]
  13. Ontario Research Fund
  14. Canadian Institutes of Health Research
  15. Cancer Risk Evaluation (CaRE) Program grant from the Canadian Cancer Society Research Institute
  16. Ontario Institute for Cancer Research through Ontario Ministry of Research and Innovation. PLCO: Intramural Research Program of the Division of Cancer Epidemiology and Genetics
  17. Division of Cancer Prevention, National Cancer Institute, NIH, DHHS

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Dietary factors, including meat, fruits, vegetables and fiber, are associated with colorectal cancer; however, there is limited information as to whether these dietary factors interact with genetic variants to modify risk of colorectal cancer. We tested interactions between these dietary factors and approximately 2.7 million genetic variants for colorectal cancer risk among 9,287 cases and 9,117 controls from ten studies. We used logistic regression to investigate multiplicative gene-diet interactions, as well as our recently developed Cocktail method that involves a screening step based on marginal associations and gene-diet correlations and a testing step for multiplicative interactions, while correcting for multiple testing using weighted hypothesis testing. Per quartile increment in the intake of red and processed meat were associated with statistically significant increased risks of colorectal cancer and vegetable, fruit and fiber intake with lower risks. From the case-control analysis, we detected a significant interaction between rs4143094 (10p14/near GATA3) and processed meat consumption (OR = 1.17; p = 8.7E-09), which was consistently observed across studies (p heterogeneity = 0.78). The risk of colorectal cancer associated with processed meat was increased among individuals with the rs4143094-TG and -TT genotypes (OR = 1.20 and OR = 1.39, respectively) and null among those with the GG genotype (OR = 1.03). Our results identify a novel gene-diet interaction with processed meat for colorectal cancer, highlighting that diet may modify the effect of genetic variants on disease risk, which may have important implications for prevention.

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