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PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3).


ABSTRACT: Genes involved in the inflammation pathway have been associated with cancer risk. Genetic variants in the interleukin-6 (IL6) and prostaglandin-endoperoxide synthase-2 (PTGS2, encoding for the COX-2 enzyme) genes, in particular, have been related to several cancer types, including breast and prostate cancers. We conducted a study within the Breast and Prostate Cancer Cohort Consortium to examine the association between IL6 and PTGS2 polymorphisms and breast and prostate cancer risk. Twenty-seven polymorphisms, selected by pairwise tagging, were genotyped on 6292 breast cancer cases and 8135 matched controls and 8008 prostate cancer cases and 8604 matched controls. The large sample sizes and comprehensive single nucleotide polymorphism tagging in this study gave us excellent power to detect modest effects for common variants. After adjustment for multiple testing, none of the associations examined remained statistically significant at P = 0.01. In analyses not adjusted for multiple testing, one IL6 polymorphism (rs6949149) was marginally associated with breast cancer risk (TT versus GG, odds ratios (OR): 1.32; 99% confidence intervals (CI): 1.00-1.74, P(trend) = 0.003) and two were marginally associated with prostate cancer risk (rs6969502-AA versus rs6969502-GG, OR: 0.87, 99% CI: 0.75-1.02; P(trend) = 0.002 and rs7805828-AA versus rs7805828-GG, OR: 1.11, 99% CI: 0.99-1.26; P(trend) = 0.007). An increase in breast cancer risk was observed for the PTGS2 polymorphism rs7550380 (TT versus GG, OR: 1.38, 99% CI: 1.04-1.83). No association was observed between PTGS2 polymorphisms and prostate cancer risk. In conclusion, common genetic variation in these two genes might play at best a limited role in breast and prostate cancers.

SUBMITTER: Dossus L 

PROVIDER: S-EPMC2832545 | biostudies-literature | 2010 Mar

REPOSITORIES: biostudies-literature

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PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3).

Dossus Laure L   Kaaks Rudolf R   Canzian Federico F   Albanes Demetrius D   Berndt Sonja I SI   Boeing Heiner H   Buring Julie J   Chanock Stephen J SJ   Clavel-Chapelon Francoise F   Feigelson Heather Spencer HS   Gaziano John M JM   Giovannucci Edward E   Gonzalez Carlos C   Haiman Christopher A CA   Hallmans Göran G   Hankinson Susan E SE   Hayes Richard B RB   Henderson Brian E BE   Hoover Robert N RN   Hunter David J DJ   Khaw Kay-Tee KT   Kolonel Laurence N LN   Kraft Peter P   Ma Jing J   Le Marchand Loic L   Lund Eiliv E   Peeters Petra H M PH   Stampfer Meir M   Stram Dan O DO   Thomas Gilles G   Thun Michael J MJ   Tjonneland Anne A   Trichopoulos Dimitrios D   Tumino Rosario R   Riboli Elio E   Virtamo Jarmo J   Weinstein Stephanie J SJ   Yeager Meredith M   Ziegler Regina G RG   Cox David G DG  

Carcinogenesis 20091204 3


Genes involved in the inflammation pathway have been associated with cancer risk. Genetic variants in the interleukin-6 (IL6) and prostaglandin-endoperoxide synthase-2 (PTGS2, encoding for the COX-2 enzyme) genes, in particular, have been related to several cancer types, including breast and prostate cancers. We conducted a study within the Breast and Prostate Cancer Cohort Consortium to examine the association between IL6 and PTGS2 polymorphisms and breast and prostate cancer risk. Twenty-seven  ...[more]

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