No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: A multi-center cohort study

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Timothy R. Rebbeck - , University of Pennsylvania (Autor:in)
  • Antonis C. Antoniou - , University of Cambridge (Autor:in)
  • Trinidad Caldes Llopis - , Hospital Clinico Universitario San Carlos (Autor:in)
  • Heli Nevanlinna - , University of Helsinki (Autor:in)
  • Kristiina Aittomäki - , University of Helsinki (Autor:in)
  • Jacques Simard - , Université Laval (Autor:in)
  • Amanda B. Spurdle - , Queensland Institute of Medical Research (Autor:in)
  • Fergus J. Couch - , Mayo Clinic Rochester, MN (Autor:in)
  • Lutecia H.Mateus Pereira - , National Cancer Institute (NCI), University of Miami (Autor:in)
  • Mark H. Greene - , National Cancer Institute (NCI) (Autor:in)
  • Irene L. Andrulis - , University of Toronto, Cancer Care Ontario (Autor:in)
  • Boris Pasche - , Northwestern University, Breast Cancer Family Registry (Autor:in)
  • Virginia Kaklamani - , Northwestern University, Breast Cancer Family Registry (Autor:in)
  • Ute Hamann - , Deutsches Krebsforschungszentrum (DKFZ) (Autor:in)
  • Csilla Szabo - , Mayo Clinic Rochester, MN (Autor:in)
  • Susan Peock - , University of Cambridge (Autor:in)
  • Margaret Cook - , University of Cambridge (Autor:in)
  • Patricia A. Harrington - , University of Cambridge (Autor:in)
  • Alan Donaldson - , University Hospitals Bristol and Weston NHS Foundation Trust (Autor:in)
  • Allison M. Male - , Great Ormond Street Hospital for Children NHS Trust (Autor:in)
  • Carol Anne Gardiner - , Nottingham University Hospitals NHS Trust (Autor:in)
  • Helen Gregory - , University of Aberdeen (Autor:in)
  • Lucy E. Side - , Churchill Hospital (Autor:in)
  • Anne C. Robinson - , Mid and South Essex NHS Foundation Trust (Autor:in)
  • Louise Emmerson - , Betsi Cadwaladr University Health Board (Autor:in)
  • Ian Ellis - , Alder Hey Children's NHS Foundation Trust (Autor:in)
  • Jean Philippe Peyrat - , Centre Oscar Lambret (Autor:in)
  • Joëlle Fournier - , Centre Oscar Lambret (Autor:in)
  • Philippe Vennin - , Centre Oscar Lambret (Autor:in)
  • Claude Adenis - , Centre Oscar Lambret (Autor:in)
  • Danièle Muller - , Centre Georges-François Leclerc (Autor:in)
  • Jean Pierre Fricker - , Centre Georges-François Leclerc (Autor:in)
  • Michel Longy - , Centre Georges-François Leclerc (Autor:in)
  • Olga M. Sinilnikova - , Universite Claude Bernard Lyon 1 (Autor:in)
  • Dominique Stoppa-Lyonnet - , Institut Curie (Autor:in)
  • Rita K. Schmutzler - , Universität zu Köln (Autor:in)
  • Beatrix Versmold - , Universität zu Köln (Autor:in)
  • Christoph Engel - , Universität Leipzig (Autor:in)
  • Alfons Meindl - , Technische Universität München (Autor:in)
  • Karin Kast - , Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe (Autor:in)
  • Dieter Schaefer - , Johann Wolfgang Goethe-Universität Frankfurt am Main (Autor:in)
  • Ursula G. Froster - , Universität Leipzig (Autor:in)
  • Georgia Chenevix-Trench - , Queensland Institute of Medical Research (Autor:in)
  • Douglas F. Easton - , University of Cambridge (Autor:in)

Abstract

Background The transforming growth factor β-1 gene (TGFB1) is a plausible candidate for breast cancer susceptibility. The L10P variant of TGFB1 is associated with higher circulating levels and secretion of TGF-β, and recent large-scale studies suggest strongly that this variant is associated with breast cancer risk in the general population. Methods To evaluate whether TGFB1 L10P also modifies the risk of breast cancer in BRCA1 or BRCA2 mutation carriers, we undertook a multi-center study of 3,442 BRCA1 and 2,095 BRCA2 mutation carriers. Results We found no evidence of association between TGFB1 L10P and breast cancer risk in either BRCA1 or BRCA2 mutation carriers. The per-allele HR for the L10P variant was 1.01 (95%CI: 0.92-1.11) in BRCA1 carriers and 0.92 (95%CI: 0.81-1.04) in BRCA2 mutation carriers. Conclusions These results do not support the hypothesis that TGFB1 L10P genotypes modify the risk of breast cancer in BRCA1 or BRCA2 mutation carriers.

Details

OriginalspracheEnglisch
Seiten (von - bis)185-192
Seitenumfang8
FachzeitschriftBreast cancer research and treatment
Jahrgang115
Ausgabenummer1
PublikationsstatusVeröffentlicht - 1 Mai 2009
Peer-Review-StatusJa

Externe IDs

PubMed 18523885

Schlagworte

Ziele für nachhaltige Entwicklung

ASJC Scopus Sachgebiete

Schlagwörter

  • BRCA1, BRCA2, Hereditary cancer, Risk modifiers