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Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy.
- Source :
-
Familial cancer [Fam Cancer] 2012 Mar; Vol. 11 (1), pp. 41-7. - Publication Year :
- 2012
-
Abstract
- Pancreatic adenocarcinoma (PC) is the third most common cancer associated with BRCA mutations. Most notice has been given to BRCA2, while the association between BRCA1 and PC is less widely reported. Recently, PALB2 has been implicated in both PC and breast cancer (BC) susceptibility. We selected 29 Italian PC patients from a case-control study of PC according to their personal and family history of both PC and breast/ovarian cancer (BC/OC) and tested them for presence of germline mutations in BRCA1, BRCA2 and PALB2. We identified no germline mutations or deletions in PALB2, but detected 7 BRCA mutations (4 in BRCA1 and 3 in BRCA2). These findings suggest that PALB2 does not play a major role in PC susceptibility in our population. As we found an almost equal frequency of germline mutations in BRCA1 and BRCA2, germline alterations in either of these genes may explain a subset of Italian families presenting both PC and BC/OC. Moreover, as we began the observation of these families from probands who are affected by PC, we provide here a direct assessment of the role of PALB2 and BRCA mutations in PC susceptibility.
- Subjects :
- Adult
Aged
Aged, 80 and over
Breast Neoplasms genetics
Case-Control Studies
Fanconi Anemia Complementation Group N Protein
Female
Genetic Predisposition to Disease
Humans
Italy
Male
Middle Aged
Ovarian Neoplasms genetics
Pedigree
Adenocarcinoma genetics
BRCA1 Protein genetics
BRCA2 Protein genetics
Gene Deletion
Germ-Line Mutation genetics
Nuclear Proteins genetics
Pancreatic Neoplasms genetics
Tumor Suppressor Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1573-7292
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Familial cancer
- Publication Type :
- Academic Journal
- Accession number :
- 21989927
- Full Text :
- https://doi.org/10.1007/s10689-011-9483-5