Source:http://linkedlifedata.com/resource/pubmed/id/12404104
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
11
|
| pubmed:dateCreated |
2002-10-29
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| pubmed:abstractText |
BRCA1/2 mutation carriers are at an increased risk for developing breast and/or ovarian cancer. Yet, the genetic and environmental factors that govern the phenotypic expression of mutant BRCA1/2 alleles remain elusive. The CAG repeat within exon 1 of the androgen receptor (AR) gene is reportedly associated with breast cancer phenotype in BRCA1 mutation carriers. Two hundred and twenty seven BRCA1/2 mutation carriers were genotyped for the polymorphic AR CAG repeat, and allele size was correlated with breast/ovarian cancer morbidity parameters. Of 227 BRCA1/2 carriers, 169 were BRCA1 mutation carriers and 58 carried a BRCA2 mutation, 149 had breast and/or ovarian cancer and 78 were asymptomatic mutation carriers. The mean age at diagnosis in women with either or both neoplasms was 46.7+/-11.2 years, and that of the asymptomatic group - 45.8+/-9.4 years, a statistically insignificant difference. The AR CAG repeat ranged from eight to 28 in all tested women, and the mean number of the repeats were not statistically different between affected (18.3+/-2.4) and asymptomatic mutation carriers (18.6+/-2.1). The AR CAG repeat among patients with early onset (<42 years) breast cancer was significantly shorter (17.5+/-2.3) compared with asymptomatic individuals (18.6+/-2.1) (P<0.01), and the shorter allele - the younger the age at diagnosis. There is no conclusive evidence of association between AR CAG repeat size and breast or ovarian cancer risk in Jewish BRCA1/2 mutation carriers. A small effect of a short AR CAG allele size on breast cancer at early age (<42 years) cannot be excluded.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:month |
Nov
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| pubmed:issn |
1018-4813
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
10
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| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
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| pubmed:pagination |
724-8
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| pubmed:dateRevised |
2004-11-17
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| pubmed:meshHeading |
pubmed-meshheading:12404104-Adult,
pubmed-meshheading:12404104-Breast Neoplasms,
pubmed-meshheading:12404104-Female,
pubmed-meshheading:12404104-Genes, BRCA1,
pubmed-meshheading:12404104-Genes, BRCA2,
pubmed-meshheading:12404104-Genotype,
pubmed-meshheading:12404104-Humans,
pubmed-meshheading:12404104-Israel,
pubmed-meshheading:12404104-Middle Aged,
pubmed-meshheading:12404104-Ovarian Neoplasms,
pubmed-meshheading:12404104-Phenotype,
pubmed-meshheading:12404104-Receptors, Androgen,
pubmed-meshheading:12404104-Trinucleotide Repeats
|
| pubmed:year |
2002
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| pubmed:articleTitle |
Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotype.
|
| pubmed:affiliation |
Institute of Human Genetics, Rambam Medical Center, Haifa, Israel.
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| pubmed:publicationType |
Journal Article
|