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PMID: 20346647 Published · ppublish English Journal Article Review

Discovering moderate-risk breast cancer susceptibility genes.

Current opinion in genetics & development ·Vol. 20 ·No. 3 ·2010-06-00 ·Pages 268-76

Hollestelle A, Wasielewski M, Martens JW, Schutte M

Abstract

To date, five moderate-risk breast cancer susceptibility genes have been convincingly identified: CHEK2, ATM, BRIP1, PALB2, and NBS1. Moderate-risk breast cancer alleles confer increased breast cancer risks of two to fourfold compared to the 10% risk in the general population. In contrast to the high-risk BRCA1 and BRCA2 genes, moderate-risk genes typically have a limited number of variants that confer breast cancer risks. The prevalence of the variants usually varies widely among different geographical or ethnic populations, ranging from essentially absent up to 1.5% (i.e. 'rare' variants). Since moderate-risk breast cancer alleles are clinically not recognizable when inherited as single mutant, one usually encounters them in a polygenic setting and consequently in incomplete cosegregation with the breast cancer phenotype. As a result, discovery of moderate-risk breast cancer genes requires conclusive statistical evidence from association studies of hundreds of breast cancer cases and population-matched controls.

MeSH Terms
Ataxia Telangiectasia Mutated Proteins Breast Neoplasms/genetics Cell Cycle Proteins/genetics Checkpoint Kinase 2 DNA-Binding Proteins/genetics Fanconi Anemia Complementation Group N Protein Fanconi Anemia Complementation Group Proteins Female Genetic Predisposition to Disease/genetics Humans Nuclear Proteins/genetics Protein Serine-Threonine Kinases/genetics RNA Helicases/genetics Risk Factors Tumor Suppressor Proteins/genetics
Chemicals
Cell Cycle Proteins DNA-Binding Proteins Fanconi Anemia Complementation Group N Protein Fanconi Anemia Complementation Group Proteins NBN protein, human Nuclear Proteins PALB2 protein, human Tumor Suppressor Proteins Checkpoint Kinase 2 ATM protein, human Ataxia Telangiectasia Mutated Proteins CHEK2 protein, human Protein Serine-Threonine Kinases BRIP1 protein, human RNA Helicases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hollestelle Antoinette
Department of Medical Oncology, Josephine Nefkens Institute, Erasmus University Medical Center, Rotterdam, The Netherlands. [email protected]
Wasielewski Marijke
Martens John W M
Schutte Mieke
Article Info
Journal
Current opinion in genetics & development
Abbr.
Curr Opin Genet Dev
ISSN
1879-0380
Published
2010-06-00
Epub
2010-00-24
Pages
268-76
Language
English
Region
England
NLM ID
9111375
Subset
IM
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