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Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics
Authors:Garcia-Closas Montserrat  Hall Per  Nevanlinna Heli  Pooley Karen  Morrison Jonathan  Richesson Douglas A  Bojesen Stig E  Nordestgaard Børge G  Axelsson Christen K  Arias Jose I  Milne Roger L  Ribas Gloria  González-Neira Anna  Benítez Javier  Zamora Pilar  Brauch Hiltrud  Justenhoven Christina  Hamann Ute  Ko Yon-Dschun  Bruening Thomas  Haas Susanne  Dörk Thilo  Schürmann Peter  Hillemanns Peter  Bogdanova Natalia  Bremer Michael  Karstens Johann Hinrich  Fagerholm Rainer  Aaltonen Kirsimari  Aittomäki Kristiina  von Smitten Karl  Blomqvist Carl  Mannermaa Arto  Uusitupa Matti  Eskelinen Matti  Tengström Maria
Affiliation:Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Marylan, United States of America. montse@nih.gov
Abstract:A three-stage genome-wide association study recently identified single nucleotide polymorphisms (SNPs) in five loci (fibroblast growth receptor 2 (FGFR2), trinucleotide repeat containing 9 (TNRC9), mitogen-activated protein kinase 3 K1 (MAP3K1), 8q24, and lymphocyte-specific protein 1 (LSP1)) associated with breast cancer risk. We investigated whether the associations between these SNPs and breast cancer risk varied by clinically important tumor characteristics in up to 23,039 invasive breast cancer cases and 26,273 controls from 20 studies. We also evaluated their influence on overall survival in 13,527 cases from 13 studies. All participants were of European or Asian origin. rs2981582 in FGFR2 was more strongly related to ER-positive (per-allele OR (95%CI) = 1.31 (1.27–1.36)) than ER-negative (1.08 (1.03–1.14)) disease (P for heterogeneity = 10−13). This SNP was also more strongly related to PR-positive, low grade and node positive tumors (P = 10−5, 10−8, 0.013, respectively). The association for rs13281615 in 8q24 was stronger for ER-positive, PR-positive, and low grade tumors (P = 0.001, 0.011 and 10−4, respectively). The differences in the associations between SNPs in FGFR2 and 8q24 and risk by ER and grade remained significant after permutation adjustment for multiple comparisons and after adjustment for other tumor characteristics. Three SNPs (rs2981582, rs3803662, and rs889312) showed weak but significant associations with ER-negative disease, the strongest association being for rs3803662 in TNRC9 (1.14 (1.09–1.21)). rs13281615 in 8q24 was associated with an improvement in survival after diagnosis (per-allele HR = 0.90 (0.83–0.97). The association was attenuated and non-significant after adjusting for known prognostic factors. Our findings show that common genetic variants influence the pathological subtype of breast cancer and provide further support for the hypothesis that ER-positive and ER-negative disease are biologically distinct. Understanding the etiologic heterogeneity of breast cancer may ultimately result in improvements in prevention, early detection, and treatment.
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