A cell culture, chromosomal and quantitative DNA analysis of a metastatic epithelioid sarcoma. Deletion 1p, a possible primary chromosomal abnormality in epithelioid sarcoma

Cancer. 1990 May 1;65(9):2006-13. doi: 10.1002/1097-0142(19900501)65:9<2006::aid-cncr2820650921>3.0.co;2-q.

Abstract

The chromosomal banding pattern and the in vitro growth characteristics of a metastatic epithelioid sarcoma are described. The cultured tumor cells retained growth characteristics as well as ultrastructural and immunohistochemical properties similar to the cells of the primary tumor. Cytogenetic analysis revealed a modal range in the diploid-hypodiploid region, a finding which was corroborated by quantitative DNA determinations of both the primary tumor and a lymph node metastasis. Fourteen different marker chromosomes were identified. The most frequent clonal rearrangement was a 1p-marker resulting from a short arm terminal deletion, i.e., del (1) (p21-22). A similar 1p- marker has previously been observed in an established epithelioid sarcoma cell line. The finding of an apparently identical 1p-marker in two of two analyzed epithelioid sarcomas suggests that this rearrangement may be a primary cytogenetic abnormality in epithelioid sarcoma. An elevated ras p21 expression was demonstrated using immunohistochemical methods. The possible involvement of the N-ras gene and/or a tumor suppressor in the 1p deletion is considered.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Aberrations / genetics*
  • Chromosome Banding
  • Chromosome Deletion*
  • Chromosome Disorders
  • DNA, Neoplasm / analysis*
  • Forearm*
  • Humans
  • Karyotyping
  • Lymphatic Metastasis
  • Male
  • Middle Aged
  • Oncogene Protein p21(ras) / analysis
  • Sarcoma / genetics*
  • Sarcoma / secondary
  • Sarcoma / ultrastructure
  • Tumor Cells, Cultured

Substances

  • DNA, Neoplasm
  • Oncogene Protein p21(ras)