Rearrangement of chromosome 1 is a frequent finding in endometrial carcinoma. An in situ hybridization study in nine endometrial carcinomas

Cancer Genet Cytogenet. 1995 Jun;81(2):109-14. doi: 10.1016/0165-4608(94)00226-2.

Abstract

Nine endometrial carcinomas were examined for numerical aberrations of the chromosomes 1,7, and X by fluorescence in situ hybridization using highly repetitive chromosome-specific probes. In addition, a combination of a centromeric and a telomeric chromosome 1 probe was applied to detect structural chromosome 1 aberrations. Chromosome aberrations were found in six tumors. In four of these, an imbalance between 1q12 and 1p36 was detected, indicating the presence of an extra 1p- chromosome. In regard to the chromosomes 7 and X, monosomies and trisomies were found. Intratumoral genetic heterogeneity in endometrial carcinomas was detectable by FISH and flow cytometry. In conclusion, our findings confirm that chromosome 1 is frequently involved in structural chromosome changes, indicating chromosome 1 to be of importance in the evolution of endometrial carcinoma.

MeSH terms

  • Adenocarcinoma / genetics*
  • Aged
  • Aged, 80 and over
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 1 / genetics*
  • Chromosomes, Human, Pair 7 / genetics
  • DNA Probes
  • Endometrial Neoplasms / genetics*
  • Female
  • Flow Cytometry
  • Gene Rearrangement / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Middle Aged
  • X Chromosome

Substances

  • DNA Probes