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Rare germline mutations in PALB2 and breast cancer risk: A population‐based study
Author(s) -
Tischkowitz Marc,
Capanu Marinela,
Sabbaghian Nelly,
Li Lili,
Liang Xiaolin,
Vallée Maxime P.,
Tavtigian Sean V.,
Concan Patrick,
Foulkes William D.,
Bernstein Leslie,
Bernstein Jonine L.,
Begg Colin B.
Publication year - 2012
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.22022
Subject(s) - palb2 , breast cancer , germline mutation , missense mutation , biology , genetics , population , germline , oncology , cancer , medicine , mutation , gene , environmental health
Abstract Germline mutations in the PALB2 gene are associated with an increased risk of developing breast cancer but little is known about the frequencies of rare variants in PALB2 and the nature of the variants that influence risk. We selected participants recruited to the Women's Environment, Cancer, and Radiation Epidemiology (WECARE) Study and screened lymphocyte DNA from cases with contralateral breast cancer ( n = 559) and matched controls with unilateral breast cancer ( n = 565) for PALB2 mutations. Five pathogenic PALB2 mutations were identified among the cases (0.9%) versus none among the controls ( P = 0.04). The first‐degree female relatives of these five carriers demonstrated significantly higher incidence of breast cancer than relatives of noncarrier cases, indicating that pathogenic PALB2 mutations confer an estimated 5.3‐fold increase in risk (95% CI: 1.8–13.2). The frequency of rare (<1% MAF) missense mutations was similar in both groups (23 vs. 21). Our findings confirm in a population‐based study setting of women with breast cancer the strong risk associated with truncating mutations in PALB2 that has been reported in family studies. Conversely, there is no evidence from this study that rare PALB2 missense mutations strongly influence breast cancer risk. Hum Mutat 33:674–680, 2012. © 2012 Wiley Periodicals, Inc.

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