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 × 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.

Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk / Gaudet MM;Kuchenbaecker KB;Vijai J;Klein RJ;Kirchhoff T;McGuffog L;Barrowdale D;Dunning AM;Lee A;Dennis J;Healey S;Dicks E;Soucy P;Sinilnikova OM;Pankratz VS;Wang X;Eldridge RC;Tessier DC;Vincent D;Bacot F;Hogervorst FB;Peock S;Stoppa-Lyonnet D;Peterlongo P;Schmutzler RK;Nathanson KL;Piedmonte M;Singer CF;Thomassen M;Hansen Tv;Neuhausen SL;Blanco I;Greene MH;Garber J;Weitzel JN;Andrulis IL;Goldgar DE;D'Andrea E;Caldes T;Nevanlinna H;Osorio A;van Rensburg EJ;Arason A;Rennert G;van den Ouweland AM;van der Hout AH;Kets CM;Aalfs CM;Wijnen JT;Ausems MG;Frost D;Ellis S;Fineberg E;Platte R;Evans DG;Jacobs C;Adlard J;Tischkowitz M;Porteous ME;Damiola F;Golmard L;Barjhoux L;Longy M;Belotti M;Ferrer SF;Mazoyer S;Spurdle AB;Manoukian S;Barile M;Genuardi M;Arnold N;Meindl A;Sutter C;Wappenschmidt B;Domchek SM;Pfeiler G;Friedman E;Jensen UB;Robson M;Shah S;Lazaro C;Mai PL;Benitez J;Southey MC;Schmidt MK;Fasching PA;Peto J;Humphreys MK;Wang Q;Michailidou K;Sawyer EJ;Burwinkel B;Guénel P;Bojesen SE;Milne RL;Brenner H;Lochmann M;Aittomäki K;Dörk T;Margolin S;Mannermaa A;Lambrechts D;Chang-Claude J;Radice P;Giles GG;Haiman CA;Winqvist R;Devillee P;García-Closas M;Schoof N;Hooning MJ;Cox A;Pharoah PD;Jakubowska A;Orr N;González-Neira A;Pita G;Alonso MR;Hall P;Couch FJ;Simard J;Altshuler D;Easton DF;Chenevix-Trench G;Antoniou AC;Offit K;KConFab Investigators;Ontario Cancer Genetics Network;HEBON;EMBRACE;GEMO Study Collaborators;GENICA Network. - In: PLOS GENETICS. - ISSN 1553-7390. - ELETTRONICO. - 9:(2013), pp. 0-0. [10.1371/journal.pgen.1003173]

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

GENUARDI, MAURIZIO;
2013

Abstract

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 × 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.
2013
9
0
0
Gaudet MM;Kuchenbaecker KB;Vijai J;Klein RJ;Kirchhoff T;McGuffog L;Barrowdale D;Dunning AM;Lee A;Dennis J;Healey S;Dicks E;Soucy P;Sinilnikova OM;Pankratz VS;Wang X;Eldridge RC;Tessier DC;Vincent D;Bacot F;Hogervorst FB;Peock S;Stoppa-Lyonnet D;Peterlongo P;Schmutzler RK;Nathanson KL;Piedmonte M;Singer CF;Thomassen M;Hansen Tv;Neuhausen SL;Blanco I;Greene MH;Garber J;Weitzel JN;Andrulis IL;Goldgar DE;D'Andrea E;Caldes T;Nevanlinna H;Osorio A;van Rensburg EJ;Arason A;Rennert G;van den Ouweland AM;van der Hout AH;Kets CM;Aalfs CM;Wijnen JT;Ausems MG;Frost D;Ellis S;Fineberg E;Platte R;Evans DG;Jacobs C;Adlard J;Tischkowitz M;Porteous ME;Damiola F;Golmard L;Barjhoux L;Longy M;Belotti M;Ferrer SF;Mazoyer S;Spurdle AB;Manoukian S;Barile M;Genuardi M;Arnold N;Meindl A;Sutter C;Wappenschmidt B;Domchek SM;Pfeiler G;Friedman E;Jensen UB;Robson M;Shah S;Lazaro C;Mai PL;Benitez J;Southey MC;Schmidt MK;Fasching PA;Peto J;Humphreys MK;Wang Q;Michailidou K;Sawyer EJ;Burwinkel B;Guénel P;Bojesen SE;Milne RL;Brenner H;Lochmann M;Aittomäki K;Dörk T;Margolin S;Mannermaa A;Lambrechts D;Chang-Claude J;Radice P;Giles GG;Haiman CA;Winqvist R;Devillee P;García-Closas M;Schoof N;Hooning MJ;Cox A;Pharoah PD;Jakubowska A;Orr N;González-Neira A;Pita G;Alonso MR;Hall P;Couch FJ;Simard J;Altshuler D;Easton DF;Chenevix-Trench G;Antoniou AC;Offit K;KConFab Investigators;Ontario Cancer Genetics Network;HEBON;EMBRACE;GEMO Study Collaborators;GENICA Network
File in questo prodotto:
File Dimensione Formato  
journal.pgen.1003173.pdf

accesso aperto

Tipologia: Pdf editoriale (Version of record)
Licenza: Creative commons
Dimensione 865.45 kB
Formato Adobe PDF
865.45 kB Adobe PDF

I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/822446
Citazioni
  • ???jsp.display-item.citation.pmc??? 68
  • Scopus 95
  • ???jsp.display-item.citation.isi??? 90
social impact