학술논문

Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO)
Document Type
Academic Journal
Source
Breast Cancer Research and Treatment. December 1, 2011, Vol. 130 Issue 3, p927, 12 p.
Subject
Gene mutations -- Health aspects
Nuclear radiation -- Health aspects
Drinking of alcoholic beverages -- Health aspects
Breast cancer -- Genetic aspects -- Risk factors -- Health aspects
Language
English
ISSN
0167-6806
Abstract
Germline mutations in BRCA1/2 confer a high risk of breast cancer (BC), but the magnitude of this risk varies according to various factors. Although controversial, there are data to support the hypothesis of allelic-risk heterogeneity. We assessed variation in BC risk according to the location of mutations recorded in the French study GENEPSO. Since the women in this study were selected from high-risk families, oversampling of affected women was eliminated by using a weighted Cox-regression model. Women were censored at the date of diagnosis when affected by any cancer, or the date of interview when unaffected. A total of 990 women were selected for the analysis: 379 were classified as affected, 611 as unaffected. For BRCA1, there was some evidence of a central region where the risk of BC is lower (codons 374-1161) (HR = 0.59, P = 0.04). For BRCA2, there was a strong evidence for a region at decreased risk (codons 957-1827) (HR = 0.35, P = 0.005) and for one at increased risk (codons 2546-2968) (HR = 3.56, P = 0.01). Moreover, we found an important association between radiation exposure from chest X-rays and BC risk (HR = 4.29, P < [10.sup.-3]) and a positive association between smoking more than 21 pack-years and BC risk (HR = 2.09, P = 0.04). No significant variation in BC risk associated with chest X-ray exposure, smoking, and alcohol consumption was found according to the location of the mutation in BRCA1 and BRCA2. Our findings are consistent with those suggesting that the risk of BC is lower in the central regions of BRCA1/2. A new high-risk region in BRCA2 is described. Taking into account environmental and lifestyle modifiers, the location of mutations might be important in the clinical management of BRCA mutation carriers. Keywords Breast cancer * Risk factor * Genotype-phenotype correlation * BRCA1 * BRCA2 * Interaction
Introduction Carriers of mutations in the BRCA1 and BRCA2 genes are at very high risk of developing breast cancer (BC) and ovarian cancer. Estimates of the lifetime risk of developing [...]