Accumulation of chromosomal changes in human glioma progression. A cytogenetic study of 50 cases

Cancer Genet Cytogenet. 1995 Nov;85(1):61-7. doi: 10.1016/0165-4608(95)00129-8.

Abstract

Cytogenetic studies of 50 human gliomas, including three oligodendrogliomas, 16 grade I-III astrocytomas, and 31 glioblastomas multiforme, were performed using the short-term tissue culture method. The most common numerical chromosome aberrations were +7, -9, -10, -14, and loss of a sex chromosome. Structural changes involved predominantly the following chromosome arms: 1q, 2q, 6q, 7q, 9p, 14q, 17p, and 18p. Losses of chromosomes 9, 10, and 14, often occurring simultaneously and in polyploid clones, were observed almost exclusively in high-grade gliomas, and appear to constitute important events during glioma progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Astrocytoma / genetics
  • Brain Neoplasms / genetics*
  • Child
  • Child, Preschool
  • Chromosome Aberrations*
  • Female
  • Glioblastoma / genetics
  • Glioma / genetics*
  • Humans
  • Karyotyping
  • Male
  • Middle Aged
  • Oligodendroglioma / genetics
  • Tumor Cells, Cultured