Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.

Gaudet Mia M,Kuchenbaecker Karoline B,Vijai Joseph,Klein Robert J,Kirchhoff Tomas,McGuffog Lesley,Barrowdale Daniel,Dunning Alison M,Lee Andrew,Dennis Joe,Healey Sue,Dicks Ed,Soucy Penny,Sinilnikova Olga M,Pankratz Vernon S,Wang Xianshu,Eldridge Ronald C,Tessier Daniel C,Vincent Daniel,Bacot Francois,Hogervorst Frans B L,Peock Susan,Stoppa-Lyonnet Dominique, Null Null,Peterlongo Paolo,Schmutzler Rita K,Nathanson Katherine L,Piedmonte Marion,Singer Christian F,Thomassen Mads, Null Null,Hansen Thomas v O,Neuhausen Susan L,Blanco Ignacio,Greene Mark H, Garber Judith,Weitzel Jeffrey N,Andrulis Irene L,Goldgar David E,D'Andrea Emma,Caldes Trinidad,Nevanlinna Heli,Osorio Ana,van Rensburg Elizabeth J,Arason Adalgeir,Rennert Gad,van den Ouweland Ans M W,van der Hout Annemarie H,Kets Carolien M,Aalfs Cora M,Wijnen Juul T,Ausems Margreet G E M, Null Null,Frost Debra,Ellis Steve,Fineberg Elena, Platte Radka,Evans D Gareth,Jacobs Chris,Adlard Julian,Tischkowitz Marc,Porteous Mary E,Damiola Francesca, Null Null,Golmard Lisa,Barjhoux Laure,Longy Michel,Belotti Muriel,Ferrer Sandra Fert,Mazoyer Sylvie,Spurdle Amanda B,Manoukian Siranoush,Barile Monica,Genuardi Maurizio,Arnold Norbert,Meindl Alfons,Sutter Christian,Wappenschmidt Barbara,Domchek Susan M,Pfeiler Georg,Friedman Eitan,Jensen Uffe Birk,Robson Mark,Shah Sohela,Lazaro Conxi,Mai Phuong L,Benitez Javier,Southey Melissa C,Schmidt Marjanka K,Fasching Peter A,Peto Julian,Humphreys Manjeet K,Wang Qin,Michailidou Kyriaki,Sawyer Elinor J,Burwinkel Barbara,Guénel Pascal,Bojesen Stig E,Milne Roger L,Brenner Hermann,Lochmann Magdalena, Null Null,Aittomäki Kristiina,Dörk Thilo,Margolin Sara,Mannermaa Arto,Lambrechts Diether,Chang-Claude Jenny,Radice Paolo,Giles Graham G,Haiman Christopher A,Winqvist Robert,Devillee Peter,García-Closas Montserrat,Schoof Nils,Hooning Maartje J,Cox Angela,Pharoah Paul D P,Jakubowska Anna,Orr Nick,González-Neira Anna,Pita Guillermo,Alonso M Rosario,Hall Per,Couch Fergus J,Simard Jacques,Altshuler David,Easton Douglas F,Chenevix-Trench Georgia,Antoniou Antonis C,Offit Kenneth

PLOS GENETICS(2013)

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摘要
Common genetic variants contribute to the observed variation in breast cancer risk for BRCA2 mutation carriers; those known to date have all been found through population-based genome-wide association studies (GWAS). To comprehensively identify breast cancer risk modifying loci for BRCA2 mutation carriers, we conducted a deep replication of an ongoing GWAS discovery study. Using the ranked P-values of the breast cancer associations with the imputed genotype of 1.4 M SNPs, 19,029 SNPs were selected and designed for inclusion on a custom Illumina array that included a total of 211,155 SNPs as part of a multi-consortial project. DNA samples from 3,881 breast cancer affected and 4,330 unaffected BRCA2 mutation carriers from 47 studies belonging to the Consortium of Investigators of Modifiers of BRCA1/2 were genotyped and available for analysis. We replicated previously reported breast cancer susceptibility alleles in these BRCA2 mutation carriers and for several regions (including FGFR2, MAP3K1, CDKN2A/B, and PTHLH) identified SNPs that have stronger evidence of association than those previously published. We also identified a novel susceptibility allele at 6p24 that was inversely associated with risk in BRCA2 mutation carriers (rs9348512; per allele HR = 0.85, 95% CI 0.80-0.90, P = 3.9 x 10(-8)). This SNP was not associated with breast cancer risk either in the general population or in BRCA1 mutation carriers. The locus lies within a region containing TFAP2A, which encodes a transcriptional activation protein that interacts with several tumor suppressor genes. This report identifies the first breast cancer risk locus specific to a BRCA2 mutation background. This comprehensive update of novel and previously reported breast cancer susceptibility loci contributes to the establishment of a panel of SNPs that modify breast cancer risk in BRCA2 mutation carriers. This panel may have clinical utility for women with BRCA2 mutations weighing options for medical prevention of breast cancer.
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关键词
mutation,molecular epidemiology,genome wide association studies,genotype,genotyping,genome wide association study,heterozygote,breast cancer,genetics,population,alleles,biology,genetic loci,risk factors,genome wide association
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