Association of ESR1 gene tagging SNPs with breast cancer risk

Research output: Contribution to journalJournal articleResearchpeer-review

  • Alison M Dunning
  • Catherine S Healey
  • Caroline Baynes
  • Ana-Teresa Maia
  • Serena Scollen
  • Ana Vega
  • Raquel Rodríguez
  • Nuno L Barbosa-Morais
  • Bruce A J Ponder
  • SEARCH
  • Yen-Ling Low
  • Sheila Bingham
  • EPIC
  • Christopher A Haiman
  • Loic Le Marchand
  • MEC
  • Annegien Broeks
  • Marjanka K Schmidt
  • ABCS
  • John Hopper
  • Melissa Southey
  • ABCFS
  • Matthias W Beckmann
  • Peter A Fasching
  • BBCC
  • Julian Peto
  • Nichola Johnson
  • BBCS
  • Bojesen, Stig Egil
  • Nordestgaard, Børge
  • CGPS
  • Roger L Milne
  • Javier Benitez
  • CNIO-BCS
  • Ute Hamann
  • Yon Ko
  • GENICA
  • Rita K Schmutzler
  • Barbara Burwinkel
  • GC-HBOC
  • Peter Schürmann
  • Thilo Dörk
  • HABCS
  • Tuomas Heikkinen
  • Heli Nevanlinna
  • HEBCS
  • Annika Lindblom
  • Sara Margolin
  • KARBAC
  • Arto Mannermaa
  • Veli-Matti Kosma
  • KBCS
  • Xiaoqing Chen
  • Amanda Spurdle
  • kConFab and the AOCS Management Group
  • Jenny Change-Claude
  • Dieter Flesch-Janys
  • MARIE
  • Fergus J Couch
  • Janet E Olson
  • for MCBCS
  • Gianluca Severi
  • Laura Baglietto
  • MCCS
  • Anne-Lise Børresen-Dale
  • Vessela Kristensen
  • NBCS
  • David J Hunter
  • Susan E Hankinson
  • NHS
  • Peter Devilee
  • ORIGO
  • PBCS
  • SASBAC
  • SEBCS
  • TWBCS
  • UCIBCS
  • USRTS
  • BCAC
We have conducted a three-stage, comprehensive single nucleotide polymorphism (SNP)-tagging association study of ESR1 gene variants (SNPs) in more than 55,000 breast cancer cases and controls from studies within the Breast Cancer Association Consortium (BCAC). No large risks or highly significant associations were revealed. SNP rs3020314, tagging a region of ESR1 intron 4, is associated with an increase in breast cancer susceptibility with a dominant mode of action in European populations. Carriers of the c-allele have an odds ratio (OR) of 1.05 [95% Confidence Intervals (CI) 1.02-1.09] relative to t-allele homozygotes, P = 0.004. There is significant heterogeneity between studies, P = 0.002. The increased risk appears largely confined to oestrogen receptor-positive tumour risk. The region tagged by SNP rs3020314 contains sequence that is more highly conserved across mammalian species than the rest of intron 4, and it may subtly alter the ratio of two mRNA splice forms.
Original languageEnglish
JournalHuman Molecular Genetics
Volume18
Issue number6
Pages (from-to)1131-9
Number of pages9
ISSN0964-6906
DOIs
Publication statusPublished - 2009

Bibliographical note

Keywords: Breast Neoplasms; Estrogen Receptor alpha; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Neoplasm Staging; Polymorphism, Single Nucleotide; RNA, Neoplasm

ID: 20569302