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Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

Author:
  • Timothy R. Rebbeck
  • Tara M. Friebel
  • Nandita Mitra
  • Fei Wan
  • Stephanie Chen
  • Irene L. Andrulis
  • Paraskevi Apostolou
  • Norbert Arnold
  • Banu K. Arun
  • Daniel Barrowdale
  • Javier Benitez
  • Raanan Berger
  • Pascaline Berthet
  • Åke Borg
  • Saundra S. Buys
  • Trinidad Caldes
  • Jonathan Carter
  • Jocelyne Chiquette
  • Kathleen B M Claes
  • Fergus J. Couch
  • Cezary Cybulski
  • Mary B. Daly
  • Miguel de la Hoya
  • Orland Diez
  • Susan M. Domchek
  • Katherine L. Nathanson
  • Katarzyna Durda
  • Steve Ellis
  • D. Gareth Evans
  • Lenka Foretova
  • Eitan Friedman
  • Debra Frost
  • Patricia A. Ganz
  • Judy Garber
  • Gord Glendon
  • Andrew K. Godwin
  • Mark H. Greene
  • Jacek Gronwald
  • Eric Hahnen
  • Emily Hallberg
  • Ute Hamann
  • Thomas V O Hansen
  • Evgeny N. Imyanitov
  • Claudine Isaacs
  • Anna Jakubowska
  • Ramunas Janavicius
  • Katarzyna Jaworska-Bieniek
  • Esther M. John
  • Beth Y. Karlan
  • Bella Kaufman
  • Ava Kwong
  • Yael Laitman
  • Christine Lasset
  • Conxi Lazaro
  • Jenny Lester
  • Niklas Loman
  • Jan Lubinski
  • Siranoush Manoukian
  • Gillian Mitchell
  • Marco Montagna
  • Susan L. Neuhausen
  • Heli Nevanlinna
  • Dieter Niederacher
  • Robert L. Nussbaum
  • Kenneth Offit
  • Edith Olah
  • Olufunmilayo I. Olopade
  • Sue Kyung Park
  • Marion Piedmonte
  • Paolo Radice
  • Christine Rappaport-Fuerhauser
  • Matti A. Rookus
  • Caroline Seynaeve
  • Jacques Simard
  • Christian F. Singer
  • Penny Soucy
  • Melissa Southey
  • Dominique Stoppa-Lyonnet
  • Grzegorz Sukiennicki
  • Csilla I. Szabo
  • Mariella Tancredi
  • Manuel R. Teixeira
  • Soo Hwang Teo
  • Mary Beth Terry
  • Mads Thomassen
  • Laima Tihomirova
  • Marc Tischkowitz
  • Amanda Ewart Toland
  • Aleksandra Toloczko-Grabarek
  • Nadine Tung
  • Elizabeth J. van Rensburg
  • Danylo Villano
  • Shan Wang-Gohrke
  • Barbara Wappenschmidt
  • Jeffrey N. Weitzel
  • Jamal Zidan
  • Kristin K. Zorn
  • Lesley McGuffog
  • Douglas Easton
  • Georgia Chenevix-Trench
  • Antonis C. Antoniou
  • Susan J. Ramus
Publishing year: 2016-11-11
Language: English
Publication/Series: Breast Cancer Research
Volume: 18
Issue: 1
Document type: Journal article
Publisher: BioMed Central

Abstract english

Background: Most BRCA1 or BRCA2 mutation carriers have inherited a single (heterozygous) mutation. Transheterozygotes (TH) who have inherited deleterious mutations in both BRCA1 and BRCA2 are rare, and the consequences of transheterozygosity are poorly understood. Methods: From 32,295 female BRCA1/2 mutation carriers, we identified 93 TH (0.3 %). "Cases" were defined as TH, and "controls" were single mutations at BRCA1 (SH1) or BRCA2 (SH2). Matched SH1 "controls" carried a BRCA1 mutation found in the TH "case". Matched SH2 "controls" carried a BRCA2 mutation found in the TH "case". After matching the TH carriers with SH1 or SH2, 91 TH were matched to 9316 SH1, and 89 TH were matched to 3370 SH2. Results: The majority of TH (45.2 %) involved the three common Jewish mutations. TH were more likely than SH1 and SH2 women to have been ever diagnosed with breast cancer (BC; p = 0.002). TH were more likely to be diagnosed with ovarian cancer (OC) than SH2 (p = 0.017), but not SH1. Age at BC diagnosis was the same in TH vs. SH1 (p = 0.231), but was on average 4.5 years younger in TH than in SH2 (p < 0.001). BC in TH was more likely to be estrogen receptor (ER) positive (p = 0.010) or progesterone receptor (PR) positive (p = 0.013) than in SH1, but less likely to be ER positive (p < 0.001) or PR positive (p = 0.012) than SH2. Among 15 tumors from TH patients, there was no clear pattern of loss of heterozygosity (LOH) for BRCA1 or BRCA2 in either BC or OC. Conclusions: Our observations suggest that clinical TH phenotypes resemble SH1. However, TH breast tumor marker characteristics are phenotypically intermediate to SH1 and SH2.

Keywords

  • Cancer and Oncology
  • Medical Genetics
  • BRCA1
  • BRCA2
  • Hereditary breast and ovarian cancer
  • Transheterozygosity

Other

Published
  • Familial Breast Cancer
  • ISSN: 1465-5411
Åke Borg
Åke Borg
E-mail: ake [dot] borg [at] med [dot] lu [dot] se

Principal investigator

Oncology and Pathology, MV

+46 46 275 25 52

MV 404 C21B2

90

Project manager

Familial Breast Cancer

90

Professor

Oncology and Pathology, MV

MV 404 C21C2

90