The role of BRCA1 and BRCA2 mutations in prostate, pancreatic and stomach cancers
The association of germline mutations in the breast cancer susceptibility gene 1 ( BRCA1 ) and the breast cancer susceptibility gene 2 ( BRCA2 ) with the development of breast and ovarian cancers have been widely researched and recognised. It is known that these genes function at multiple sites in t...
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Published in | Hereditary cancer in clinical practice Vol. 13; no. 1; p. 16 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
01.08.2015
BioMed Central Ltd |
Subjects | |
Online Access | Get full text |
ISSN | 1897-4287 1731-2302 1897-4287 |
DOI | 10.1186/s13053-015-0038-x |
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Summary: | The association of germline mutations in the breast cancer susceptibility gene 1 (
BRCA1
) and the breast cancer susceptibility gene 2 (
BRCA2
) with the development of breast and ovarian cancers have been widely researched and recognised. It is known that these genes function at multiple sites in the body. Research has subsequently evolved into the connection of
BRCA1/2
with cancers at other sites within the body. This review examines the association of
BRCA1/2
germline gene mutations with prostate, pancreatic and stomach cancers. An extensive literature search revealed conflicting findings regarding the association of
BRCA1/2
gene mutations with these cancers. Most studies suggest that there is an association between
BRCA1/2
mutations and carcinoma of the prostate, pancreas and stomach, but some reports propose that such a correlation may be due to factors other than possessing a mutated
BRCA1/2
gene, and other associations may be revealed as further epidemiological information becomes available. The review concludes that as more knowledge arises about the mechanisms of
BRCA1/2
gene mutations, it should pave the way for future screening programmes to be applied effectively. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1897-4287 1731-2302 1897-4287 |
DOI: | 10.1186/s13053-015-0038-x |