BRCA1 and BRCA2 as ovarian cancer susceptibility genes.

Abstract:

:Individuals carrying germline mutations in one allele of the BRCA1 or BRCA2 genes are at significantly increased risk of developing cancer. Although the increased risk of breast cancer is often highlighted, cancer at several other sites is also considerably more common in these individuals. Here, we discuss existing knowledge of the role of BRCA1 and BRCA2 mutation in pre-disposition to ovarian cancer. The risk of an individual with a mutation developing cancer of the ovary appears to be influenced by the position of the mutation within the BRCA gene, the presence of allelic variants of modifying genes and the hormonal exposure of the carrier. Once cancer has developed, the pathology and clinical behaviour of BRCA-associated tumours is distinct from sporadic cases. Comparison of the pathogenesis of breast and ovarian cancers caused by BRCA mutation provides insight into the function of BRCA proteins as tumour suppressors in different cellular environments.

journal_name

Carcinogenesis

journal_title

Carcinogenesis

authors

Sowter HM,Ashworth A

doi

10.1093/carcin/bgi136

keywords:

subject

Has Abstract

pub_date

2005-10-01 00:00:00

pages

1651-6

issue

10

eissn

0143-3334

issn

1460-2180

pii

bgi136

journal_volume

26

pub_type

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