Defining the Smallest Common Region of Chromosome 17p that is Deleted in Sporadic Breast Tumors.

Abstract

Germline mutations in breast cancer susceptibility genes account for 8% of all breast cancer cases. BRCA1 on 17q12 and BRCA2 on 13q12-13 are implicated in 50%-60% of breast cancer families, and they are both likely to also have an impact in sporadic breast cancer cases. Recently defined loci on chromosome 8p 12-22 are frequently lost in sporadic breast cancers and there is evidence for families with linkage to these loci. We propose to ascertain 8 ethically diverse (non-Caucasian) families linked to putative BRCA3 loci on chromosome 8p, and to investigate whether a recently isolated prostate cancer metastases suppressor gene, KAII, is involved in the genetic alterations of inflammatory breast cancer, a particularly aggressive form of breast cancer which accounts for 15% of all cases.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1996
Accession Number
ADA322215

Entities

People

  • Max S. Wicha
  • Sofia D Merajver

Organizations

  • University of Michigan

Tags

DTIC Thesaurus Topics

  • African Americans
  • Breast Cancer
  • Chromosomes
  • Diseases And Disorders
  • Genes
  • Genetic Phenomena
  • Genetic Structures
  • Genetics
  • Health Services
  • Materials
  • Medical Personnel
  • Minority Groups
  • Mutations
  • Neoplasms
  • Oncology
  • Physicians
  • Suppressors

Readers

  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology