Format

Send to

Choose Destination
See comment in PubMed Commons below
Genet Mol Biol. 2009 Jul;32(3):437-46. doi: 10.1590/S1415-47572009005000049. Epub 2009 Sep 1.

Genomic rearrangements in BRCA1 and BRCA2: A literature review.

Author information

1
Laboratório de Medicina Genômica, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS Brazil.

Abstract

Women with mutations in the breast cancer genes BRCA1 or BRCA2 have an increased lifetime risk of developing breast, ovarian and other BRCA-associated cancers. However, the number of detected germline mutations in families with hereditary breast and ovarian cancer (HBOC) syndrome is lower than expected based upon genetic linkage data. Undetected deleterious mutations in the BRCA genes in some high-risk families are due to the presence of intragenic rearrangements such as deletions, duplications or insertions that span whole exons. This article reviews the molecular aspects of BRCA1 and BRCA2 rearrangements and their frequency among different populations. An overview of the techniques used to screen for large rearrangements in BRCA1 and BRCA2 is also presented. The detection of rearrangements in BRCA genes, especially BRCA1, offers a promising outlook for mutation screening in clinical practice, particularly in HBOC families that test negative for a germline mutation assessed by traditional methods.

KEYWORDS:

BRCA1; BRCA2; MLPA; breast cancer; genomic rearrangements

PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for PubMed Central
    Loading ...
    Support Center