Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium.

Publication Type:

Journal Article

Authors:

Gaudet, Mia M; Milne, Roger L; Cox, Angela; Camp, Nicola J; Goode, Ellen L; Humphreys, Manjeet K; Dunning, Alison M; Morrison, Jonathan; Giles, Graham G; Severi, Gianluca; Baglietto, Laura; English, Dallas R; Couch, Fergus J; Olson, Janet E; Wang, Xianshu; Chang-Claude, Jenny; Flesch-Janys, Dieter; Abbas, Sascha; Salazar, Ramona; Mannermaa, Arto; Kataja, Vesa; Kosma, Veli-Matti; Lindblom, Annika; Margolin, Sara; Heikkinen, Tuomas; Kämpjärvi, Kati; Aaltonen, Kirsimari; Nevanlinna, Heli; Bogdanova, Natalia; Coinac, Irina; Schürmann, Peter; Dörk, Thilo; Bartram, Claus R; Schmutzler, Rita K; Tchatchou, Sandrine; Burwinkel, Barbara; Brauch, Hiltrud; Torres, Diana; Hamann, Ute; Justenhoven, Christina; Ribas, Gloria; Arias, José I; Benitez, Javier; Bojesen, Stig E; Nordestgaard, Børge G; Flyger, Henrik L; Peto, Julian; Fletcher, Olivia; Johnson, Nichola; dos Santos Silva, Isabel; Fasching, Peter A; Beckmann, Matthias W; Strick, Reiner; Ekici, Arif B; Broeks, Annegien; Schmidt, Marjanka K; van Leeuwen, Flora E; Van't Veer, Laura J; Southey, Melissa C; Hopper, John L; Apicella, Carmel; Haiman, Christopher A; Henderson, Brian E; Le Marchand, Loic; Kolonel, Laurence N; Kristensen, Vessela; Grenaker Alnaes, Grethe; Hunter, David J; Kraft, Peter; Cox, David G; Hankinson, Susan E; Seynaeve, Caroline; Vreeswijk, Maaike P G; Tollenaar, Rob A E M; Devilee, Peter; Chanock, Stephen; Lissowska, Jolanta; Brinton, Louise; Peplonska, Beata; Czene, Kamila; Hall, Per; Li, Yuqing; Liu, Jianjun; Balasubramanian, Sabapathy; Rafii, Saeed; Reed, Malcolm W R; Pooley, Karen A; Conroy, Don; Baynes, Caroline; Kang, Daehee; Yoo, Keun-Young; Noh, Dong-Young; Ahn, Sei-Hyun; Shen, Chen-Yang; Wang, Hui-Chun; Yu, Jyh-Cherng; Wu, Pei-Ei; Anton-Culver, Hoda; Ziogoas, Argyrios; Egan, Kathleen; Newcomb, Polly A; Titus-Ernstoff, Linda; Trentham Dietz, Amy; Sigurdson, Alice J; Alexander, Bruce H; Bhatti, Parveen; Allen-Brady, Kristina; Cannon-Albright, Lisa A; Wong, Jathine; Chenevix-Trench, Georgia; Spurdle, Amanda B; Beesley, Jonathan; Pharoah, Paul D P; Easton, Doug F; Garcia-Closas, Montserrat

Source:

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Volume 18, Issue 5, p.1610-6 (2009)

Keywords:

2009, Alleles, BH3 Interacting Domain Death Agonist Protein, Breast Neoplasms, Case-Control Studies, Caspase 10, Center-Authored Paper, DNA-Binding Proteins, Europe, Female, Genetic Predisposition to Disease, Genotype, Humans, Intracellular Signaling Peptides and Proteins, Logistic Models, Nuclear Proteins, Polymorphism, Single Nucleotide, Public Health Sciences Division, RISK, Tumor Necrosis Factor-alpha

Abstract:

Previous studies have suggested that minor alleles for ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 may influence breast cancer risk, but the evidence is inconclusive due to their small sample size. These polymorphisms were genotyped in more than 30,000 breast cancer cases and 30,000 controls, primarily of European descent, from 30 studies in the Breast Cancer Association Consortium. We calculated odds ratios (OR) and 95% confidence intervals (95% CI) as a measure of association. We found that the minor alleles for these polymorphisms were not related to invasive breast cancer risk overall in women of European descent: ECCR4 per-allele OR (95% CI) = 0.99 (0.97-1.02), minor allele frequency = 27.5%; TNF 1.00 (0.95-1.06), 5.0%; CASP10 1.02 (0.98-1.07), 6.5%; PGR 1.02 (0.99-1.06), 15.3%; and BID 0.98 (0.86-1.12), 1.7%. However, we observed significant between-study heterogeneity for associations with risk for single-nucleotide polymorphisms (SNP) in CASP10, PGR, and BID. Estimates were imprecise for women of Asian and African descent due to small numbers and lower minor allele frequencies (with the exception of BID SNP). The ORs for each copy of the minor allele were not significantly different by estrogen or progesterone receptor status, nor were any significant interactions found between the polymorphisms and age or family history of breast cancer. In conclusion, our data provide persuasive evidence against an overall association between invasive breast cancer risk and ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 genotypes among women of European descent.