Breast Cancer Susceptibility Genes in High Risk Women

Abstract

A positive family history, present in about 30% of breast cancer cases, has been shown to double a woman's risk of breast cancer. The genetic factors responsible are largely unknown, although the autosomal dominant, relatively high penetrant genes BRCA1/2 may account for 3%. It has been hypothesized that susceptibility genes of lower penetrance may also affect breast cancer risk, and a likely group of such genes are those that regulate the production, intracellular transport, and metabolism of estrogen. Previous studies of these susceptibility genes have not been conducted with women with high familial risk. This study is being conducted with identical twins with differing genetic risks (i.e. concordant for breast cancer pairs vs. discordant pairs) as well as unaffected controls. We have chosen to focus on those genes related to estrogen metabolism and carcinogen metabolism. In the estrogen metabolism pathway, polymorphisms have been described related to the CYP17 gene, the CYP 19 gene, the COMT gene, and the HSD17B1 gene. Genes related to carcinogen metabolism which have been linked to breast cancer risk include GSTM1 and Pt and CYP1A1. We will compare the frequency of selected polymorphisms in these genes in 200 breast cancer concordant, 200 discordant, and 200 control women. We currently have tissue or buccal smears and informed consents from 130 concordant, 152 discordant, and 133 control women. Laboratory analyses of the CYP17 gene have shown some inconsistencies with repeat testing and additional testing is being done to assure that the results are accurate. Once the assay method has been validated, additional genes will be tested..

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2003
Accession Number
ADA418351

Entities

People

  • Ann S Hamilton

Organizations

  • University of Southern California

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Breast Cancer
  • Cancer
  • Carcinogens
  • Department Of Defense
  • Diseases And Disorders
  • Estrogens
  • Genetics
  • Health Services
  • Hormones
  • Institutional Review Board
  • Neoplasms
  • New England
  • Public Health
  • Risk Factors
  • Therapy

Fields of Study

  • Medicine

Readers

  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology