Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

Abstract

Mutations in the BRCA1 gene substantially increase a woman's lifetime risk of breast cancer. However, there is great variation in this increase in risk with several genetic and non-genetic modifiers identified. The BRCA1 protein plays a central role in DNA repair, a mechanism that is particularly instrumental in safeguarding cells against tumorigenesis. We hypothesized that polymorphisms that alter the expression and/or function of BRCA1 carried on the wild-type (non-mutated) copy of the BRCA1 gene would modify the risk of breast cancer in carriers of BRCA1 mutations. A total of 9874 BRCA1 mutation carriers were available in the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) for haplotype analyses of BRCA1. Women carrying the rare allele of single nucleotide polymorphism rs16942 on the wild-type copy of BRCA1 were at decreased risk of breast cancer (hazard ratio 0.86, 95% confidence interval 0.77-0.95, P = 0.003). Promoter in vitro assays of the major BRCA1 haplotypes showed that common polymorphisms in the regulatory region alter its activity and that this effect may be attributed to the differential binding affinity of nuclear proteins. In conclusion, variants on the wild-type copy of BRCA1 modify risk of breast cancer among carriers of BRCA1 mutations, possibly by altering the efficiency of BRCA1 transcription.

Detaljer

Författare
  • David G. Cox
  • Jacques Simard
  • Daniel Sinnett
  • Yosr Hamdi
  • Penny Soucy
  • Manon Ouimet
  • Laure Barjhoux
  • Carole Verny-Pierre
  • Lesley McGuffog
  • Sue Healey
  • Csilla Szabo
  • Mark H. Greene
  • Phuong L. Mai
  • Irene L. Andrulis
  • Mads Thomassen
  • Anne-Marie Gerdes
  • Maria A. Caligo
  • Eitan Friedman
  • Yael Laitman
  • Bella Kaufman
  • Shani S. Paluch
  • Per Karlsson
  • Marie Stenmark Askmalm
  • Gisela Barbany Bustinza
  • Katherine L. Nathanson
  • Susan M. Domchek
  • Timothy R. Rebbeck
  • Javier Benitez
  • Ute Hamann
  • Matti A. Rookus
  • Ans M. W. van den Ouweland
  • Margreet G. E. M. Ausems
  • Cora M. Aalfs
  • Christi J. van Asperen
  • Peter Devilee
  • Hans J. J. P. Gille
  • Susan Peock
  • Debra Frost
  • D. Gareth Evans
  • Ros Eeles
  • Louise Izatt
  • Julian Adlard
  • Joan Paterson
  • Jacqueline Eason
  • Andrew K. Godwin
  • Marie-Alice Remon
  • Virginie Moncoutier
  • Marion Gauthier-Villars
  • Christine Lasset
  • Sophie Giraud
  • Agnes Hardouin
  • Pascaline Berthet
  • Hagay Sobol
  • Francois Eisinger
  • Brigitte Bressac de Paillerets
  • Olivier Caron
  • Capucine Delnatte
  • David Goldgar
  • Alex Miron
  • Hilmi Ozcelik
  • Saundra Buys
  • Melissa C. Southey
  • Mary Beth Terry
  • Christian F. Singer
  • Anne-Catharina Dressler
  • Muy-Kheng Tea
  • Thomas V. O. Hansen
  • Oskar Johannsson
  • Marion Piedmonte
  • Gustavo C. Rodriguez
  • Jack B. Basil
  • Stephanie Blank
  • Amanda E. Toland
  • Marco Montagna
  • Claudine Isaacs
  • Ignacio Blanco
  • Simon A. Gayther
  • Kirsten B. Moysich
  • Rita K. Schmutzler
  • Barbara Wappenschmidt
  • Christoph Engel
  • Alfons Meindl
  • Nina Ditsch
  • Norbert Arnold
  • Dieter Niederacher
  • Christian Sutter
  • Dorothea Gadzicki
  • Britta Fiebig
  • Trinidad Caldes
  • Rachel Laframboise
  • Heli Nevanlinna
  • Xiaoqing Chen
  • Jonathan Beesley
  • Amanda B. Spurdle
  • Susan L. Neuhausen
  • Yuan C. Ding
  • Fergus J. Couch
  • Xianshu Wang
  • Paolo Peterlongo
  • Siranoush Manoukian
  • Loris Bernard
  • Paolo Radice
  • Douglas F. Easton
  • Georgia Chenevix-Trench
  • Antonis C. Antoniou
  • Dominique Stoppa-Lyonnet
  • Sylvie Mazoyer
  • Olga M. Sinilnikova
Enheter & grupper
Externa organisationer
  • Skåne University Hospital
Forskningsområden

Ämnesklassifikation (UKÄ) – OBLIGATORISK

  • Medicinsk genetik
Originalspråkengelska
Sidor (från-till)4732-4747
TidskriftHuman Molecular Genetics
Volym20
Utgivningsnummer23
StatusPublished - 2011
PublikationskategoriForskning
Peer review utfördJa