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Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.
Nan, Hongmei; Hutter, Carolyn M; Lin, Yi; Jacobs, Eric J; Ulrich, Cornelia M; White, Emily; Baron, John A; Berndt, Sonja I; Brenner, Hermann; Butterbach, Katja; Caan, Bette J; Campbell, Peter T; Carlson, Christopher S; Casey, Graham; Chang-Claude, Jenny; Chanock, Stephen J; Cotterchio, Michelle; Duggan, David; Figueiredo, Jane C; Fuchs, Charles S; Giovannucci, Edward L; Gong, Jian; Haile, Robert W; Harrison, Tabitha A; Hayes, Richard B; Hoffmeister, Michael; Hopper, John L; Hudson, Thomas J; Jenkins, Mark A; Jiao, Shuo; Lindor, Noralane M; Lemire, Mathieu; Le Marchand, Loic; Newcomb, Polly A; Ogino, Shuji; Pflugeisen, Bethann M; Potter, John D; Qu, Conghui; Rosse, Stephanie A; Rudolph, Anja; Schoen, Robert E; Schumacher, Fredrick R; Seminara, Daniela; Slattery, Martha L; Thibodeau, Stephen N; Thomas, Fridtjof; Thornquist, Mark; Warnick, Greg S; Zanke, Brent W; Gauderman, W James.
Afiliação
  • Nan H; Department of Epidemiology, Richard M. Fairbanks School of Public Health, Indiana University, Indianapolis2Indiana University Melvin and Bren Simon Cancer Center, Indianapolis.
  • Hutter CM; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
  • Lin Y; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Jacobs EJ; Epidemiology Research Program, American Cancer Society, Atlanta, Georgia.
  • Ulrich CM; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington6Huntsman Cancer Institute, University of Utah, Salt Lake City.
  • White E; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington7Department of Epidemiology, University of Washington School of Public Health, Seattle.
  • Baron JA; Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill.
  • Berndt SI; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Brenner H; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany11German Cancer Consortium (DKTK), Heidelberg, Germany.
  • Butterbach K; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Caan BJ; Division of Research, Kaiser Permanente Medical Care Program of Northern California, Oakland.
  • Campbell PT; Epidemiology Research Program, American Cancer Society, Atlanta, Georgia.
  • Carlson CS; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Casey G; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles.
  • Chang-Claude J; Division of Cancer Epidemiology, German Cancer Research Center, Heidelberg, Germany.
  • Chanock SJ; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Cotterchio M; Prevention and Cancer Control, Cancer Care Ontario, Toronto, Ontario, Canada.
  • Duggan D; Genetic Basis of Human Disease Division, Translational Genomics Research Institute (TGen), Phoenix, Arizona.
  • Figueiredo JC; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles.
  • Fuchs CS; Department of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
  • Giovannucci EL; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massacusetts.
  • Gong J; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Haile RW; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles.
  • Harrison TA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Hayes RB; Division of Epidemiology, Department of Population Health, New York University School of Medicine, New York, New York.
  • Hoffmeister M; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Hopper JL; Melbourne School of Population Health, University of Melbourne, Victoria, Australia.
  • Hudson TJ; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada22Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
  • Jenkins MA; Melbourne School of Population Health, University of Melbourne, Victoria, Australia.
  • Jiao S; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Lindor NM; Department of Health Sciences Research, Mayo Clinic, Scottsdale, Arizona.
  • Lemire M; Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
  • Le Marchand L; Epidemiology Program, University of Hawaii Cancer Center, Honolulu.
  • Newcomb PA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Ogino S; Department of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts25Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts26Department of Epidemiology, Harvard School of Public Health, Boston, Masschusetts.
  • Pflugeisen BM; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Potter JD; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington27Centre for Public Health Research, Massey University, Wellington, New Zealand.
  • Qu C; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Rosse SA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • 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.
  • Schumacher FR; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles.
  • Seminara D; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
  • Slattery ML; Department of Internal Medicine, University of Utah Health Sciences Center, Salt Lake City.
  • Thibodeau SN; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota31Department of Medical Genetics, Mayo Clinic, Rochester, Minnesota.
  • Thomas F; Division of Biostatistics and Epidemiology, Department of Preventive Medicine, University of Tennessee Healthy Science Center, Memphis.
  • Thornquist M; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Warnick GS; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Zanke BW; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Gauderman WJ; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles.
JAMA ; 313(11): 1133-42, 2015 Mar 17.
Article em En | MEDLINE | ID: mdl-25781442
IMPORTANCE: Use of aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) is associated with lower risk of colorectal cancer. OBJECTIVE: To identify common genetic markers that may confer differential benefit from aspirin or NSAID chemoprevention, we tested gene × environment interactions between regular use of aspirin and/or NSAIDs and single-nucleotide polymorphisms (SNPs) in relation to risk of colorectal cancer. DESIGN, SETTING, AND PARTICIPANTS: Case-control study using data from 5 case-control and 5 cohort studies initiated between 1976 and 2003 across the United States, Canada, Australia, and Germany and including colorectal cancer cases (n=8634) and matched controls (n=8553) ascertained between 1976 and 2011. Participants were all of European descent. EXPOSURES: Genome-wide SNP data and information on regular use of aspirin and/or NSAIDs and other risk factors. MAIN OUTCOMES AND MEASURES: Colorectal cancer. RESULTS: Regular use of aspirin and/or NSAIDs was associated with lower risk of colorectal cancer (prevalence, 28% vs 38%; odds ratio [OR], 0.69 [95% CI, 0.64-0.74]; P = 6.2 × 10(-28)) compared with nonregular use. In the conventional logistic regression analysis, the SNP rs2965667 at chromosome 12p12.3 near the MGST1 gene showed a genome-wide significant interaction with aspirin and/or NSAID use (P = 4.6 × 10(-9) for interaction). Aspirin and/or NSAID use was associated with a lower risk of colorectal cancer among individuals with rs2965667-TT genotype (prevalence, 28% vs 38%; OR, 0.66 [95% CI, 0.61-0.70]; P = 7.7 × 10(-33)) but with a higher risk among those with rare (4%) TA or AA genotypes (prevalence, 35% vs 29%; OR, 1.89 [95% CI, 1.27-2.81]; P = .002). In case-only interaction analysis, the SNP rs16973225 at chromosome 15q25.2 near the IL16 gene showed a genome-wide significant interaction with use of aspirin and/or NSAIDs (P = 8.2 × 10(-9) for interaction). Regular use was associated with a lower risk of colorectal cancer among individuals with rs16973225-AA genotype (prevalence, 28% vs 38%; OR, 0.66 [95% CI, 0.62-0.71]; P = 1.9 × 10(-30)) but was not associated with risk of colorectal cancer among those with less common (9%) AC or CC genotypes (prevalence, 36% vs 39%; OR, 0.97 [95% CI, 0.78-1.20]; P = .76). CONCLUSIONS AND RELEVANCE: In this genome-wide investigation of gene × environment interactions, use of aspirin and/or NSAIDs was associated with lower risk of colorectal cancer, and this association differed according to genetic variation at 2 SNPs at chromosomes 12 and 15. Validation of these findings in additional populations may facilitate targeted colorectal cancer prevention strategies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Anti-Inflamatórios não Esteroides / Aspirina / Polimorfismo de Nucleotídeo Único / Interação Gene-Ambiente Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: JAMA Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Anti-Inflamatórios não Esteroides / Aspirina / Polimorfismo de Nucleotídeo Único / Interação Gene-Ambiente Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: JAMA Ano de publicação: 2015 Tipo de documento: Article