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Genome-wide diet-gene interaction analyses for risk of colorectal cancer.
Figueiredo, Jane C; Hsu, Li; Hutter, Carolyn M; Lin, Yi; Campbell, Peter T; Baron, John A; Berndt, Sonja I; Jiao, Shuo; Casey, Graham; Fortini, Barbara; Chan, Andrew T; Cotterchio, Michelle; Lemire, Mathieu; Gallinger, Steven; Harrison, Tabitha A; Le Marchand, Loic; Newcomb, Polly A; Slattery, Martha L; Caan, Bette J; Carlson, Christopher S; Zanke, Brent W; Rosse, Stephanie A; Brenner, Hermann; Giovannucci, Edward L; Wu, Kana; Chang-Claude, Jenny; Chanock, Stephen J; Curtis, Keith R; Duggan, David; Gong, Jian; Haile, Robert W; Hayes, Richard B; Hoffmeister, Michael; Hopper, John L; Jenkins, Mark A; Kolonel, Laurence N; Qu, Conghui; Rudolph, Anja; Schoen, Robert E; Schumacher, Fredrick R; Seminara, Daniela; Stelling, Deanna L; Thibodeau, Stephen N; Thornquist, Mark; Warnick, Greg S; Henderson, Brian E; Ulrich, Cornelia M; Gauderman, W James; Potter, John D; White, Emily.
Afiliação
  • Figueiredo JC; Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
  • Hsu L; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Hutter CM; Division of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, Maryland, United States of America.
  • Lin Y; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Campbell PT; Epidemiology Research Program, American Cancer Society, Atlanta, Georgia, United States of America.
  • Baron JA; Department of Medicine, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Berndt SI; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America.
  • Jiao S; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Casey G; Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
  • Fortini B; Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
  • Chan AT; Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts; Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
  • Cotterchio M; Cancer Care Ontario, Toronto, Ontario, Canada.
  • Lemire M; Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
  • Gallinger S; Department of Surgery, University Health Network Toronto General Hospital, Toronto, Ontario, Canada.
  • Harrison TA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Le Marchand L; Epidemiology Program, University of Hawaii Cancer Center, Honolulu, Hawaii, United States of America.
  • Newcomb PA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Slattery ML; Department of Internal Medicine, University of Utah Health Sciences Center, Salt Lake City, Utah, United States of America.
  • Caan BJ; Division of Research, Kaiser Permanente Medical Care Program, Oakland, California, United States of America.
  • Carlson CS; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Zanke BW; Division of Hematology, Faculty of Medicine, The University of Ottawa, Ottawa, Ontario, Canada.
  • Rosse SA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Brenner H; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany.
  • Giovannucci EL; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts, United States of America.
  • Wu K; Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, United States of America.
  • Chang-Claude J; Division of Cancer Epidemiology, German Cancer Research Center, Heidelberg, Germany.
  • Chanock SJ; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America.
  • Curtis KR; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Duggan D; Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Gong J; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Haile RW; Stanford Cancer Institute, Palo Alto, California, United States of America.
  • Hayes RB; Division of Epidemiology, New York University School of Medicine, New York, New York, United States of America.
  • Hoffmeister M; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany.
  • Hopper JL; Melbourne School of Population Health, The University of Melbourne, Melbourne, Australia.
  • Jenkins MA; Melbourne School of Population Health, The University of Melbourne, Melbourne, Australia.
  • Kolonel LN; Epidemiology Program, University of Hawaii Cancer Center, Honolulu, Hawaii, United States of America.
  • Qu C; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Rudolph A; Division of Cancer Epidemiology, German Cancer Research Center, Heidelberg, Germany.
  • Schoen RE; Department of Medicine and Epidemiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States of America.
  • Schumacher FR; Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
  • Seminara D; Division of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, Maryland, United States of America.
  • Stelling DL; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Thibodeau SN; Departments of Laboratory Medicine and Pathology and Laboratory Genetics, Mayo Clinic, Rochester, Minnesota, United States of America.
  • Thornquist M; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Warnick GS; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Henderson BE; Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
  • Ulrich CM; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America; Division of Preventive Oncology, National Center for Tumor Diseases and German Cancer Research Center, Heidelberg, Germany.
  • Gauderman WJ; Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
  • Potter JD; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America; Centre for Public Health Research, Massey University, Wellington, New Zealand.
  • White E; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
PLoS Genet ; 10(4): e1004228, 2014 Apr.
Article em En | MEDLINE | ID: mdl-24743840
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Dieta Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Dieta Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article