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PMID: 8550241 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Risk modifiers in carriers of BRCA1 mutations.

International journal of cancer ·Vol. 64 ·No. 6 ·1995-12-20 ·Pages 394-8

Narod SA, Goldgar D, Cannon-Albright L, Weber B, Moslehi R, Ives E, Lenoir G, Lynch H

Abstract

The majority of, but not all, women with mutations in the BRCA1 gene will be affected with breast or ovarian cancer by the age of 70. To establish whether known risk factors modify susceptibility to cancer in these women, we have studied the reproductive histories of 333 North American women who were found by haplotype analysis to carry BRCA1 mutations. An increased risk for breast cancer was associated with low parity and with recent birth cohort. The risk of ovarian cancer decreased with increasing age at last childbirth; however, in contrast to the case for sporadic cancer, the risk of ovarian cancer in BRCA1 carriers was found to increase significantly with increasing parity.

MeSH Terms
Adult BRCA1 Protein Breast Neoplasms/etiology,genetics Female Genetic Markers Heterozygote Humans Middle Aged Mutation Neoplasm Proteins/genetics Ovarian Neoplasms/etiology,genetics Predictive Value of Tests Risk Factors Transcription Factors/genetics
Chemicals
BRCA1 Protein Genetic Markers Neoplasm Proteins Transcription Factors
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Narod S A
Department of Medicine, McGill University, Montreal, Canada.
Goldgar D
Cannon-Albright L
Weber B
Moslehi R
Ives E
Lenoir G
Lynch H
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1995-12-20
Pages
394-8
Language
English
Region
United States
NLM ID
0042124
Subset
IM
Grants
NCI NIH HHS · 1R01 CA 63678-01 · United States
NCI NIH HHS · CA-57601 · United States
NCI NIH HHS · CA-61231 · United States
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