BRCA2, but not BRCA1, mutations account for familial ovarian cancer in Iceland: a population-based study
A single founder mutation in each of the BRCA genes has been identified in Iceland. The frequency of the BRCA1 G5193A and BRCA2 999del5 mutations in all ovarian cancer patients diagnosed over the period 1991–2000 was determined. Mutation status was correlated with family history, tumour morphology a...
Saved in:
Published in: | European journal of cancer (1990) Vol. 40; no. 18; pp. 2788 - 2793 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford
Elsevier Ltd
01-12-2004
Elsevier |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | A single founder mutation in each of the BRCA genes has been identified in Iceland. The frequency of the
BRCA1 G5193A and
BRCA2 999del5 mutations in all ovarian cancer patients diagnosed over the period 1991–2000 was determined. Mutation status was correlated with family history, tumour morphology and age at diagnosis. Samples from 86% of cases (179 carcinomas and 74 borderline tumours) were available. In the carcinomas,
BRCA1 and
BRCA2 mutations were present in 1.2% and 6% of cases, respectively. No BRCA mutations were found in the borderline tumours. Odds Ratio (OR) of developing ovarian cancer was 20.65 for
BRCA2 carriers. Family history of breast/ovarian cancer was present for 70% of
BRCA2 carriers and approximately 14% for non-carriers with carcinoma. In conclusion,
BRCA2 999del5 is present in 6% of ovarian cancer cases in Iceland and is associated with a 20-fold increase in the risk of the disease. The
BRCA1 G5193A mutation is too rare to contribute significantly to ovarian cancer in Iceland. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0959-8049 1879-0852 |
DOI: | 10.1016/j.ejca.2004.09.008 |