A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma

Cancer Res. 1995 Jun 15;55(12):2494-6.

Abstract

Karyotypic and molecular data indicate that genetic alterations of the long arm of chromosome 11 (11q) may be involved in malignant melanoma. To test this we analyzed 5 polymorphic microsatellite repeats on 11q using a PCR-based assay for loss of heterozygosity in normal and tumor tissues from 24 individuals with cutaneous malignant melanoma of various stages. Our findings indicate that a tumor suppressor gene that plays a role in malignant melanoma is located on the long arm of chromosome 11, likely within a 51 cM region at 11q23. Its loss appears to be a late event in tumor progression and may serve as an indicator for a less favorable clinical outcome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Chromosome Banding
  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 11*
  • DNA / blood
  • DNA, Neoplasm / analysis
  • Genetic Markers
  • Humans
  • Lymphocytes / pathology
  • Melanoma / blood
  • Melanoma / genetics*
  • Melanoma / pathology
  • Middle Aged
  • Neoplasm Staging
  • Predictive Value of Tests
  • Skin Neoplasms / blood
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology

Substances

  • DNA, Neoplasm
  • Genetic Markers
  • DNA