Genetic abnormalities in oligodendroglial and ependymal tumours

J Neurol. 2001 Dec;248(12):1030-5. doi: 10.1007/s004150170021.

Abstract

Oligodendroglial and ependymal tumours are not the most common glial neoplasms; however, they are important subtypes of gliomas with different tumour biologies. Cytogenetic information has suggested that losses of chromosomes 1 p and 19 q are the most frequent genetic alterations in oligodendroglial tumours. Combined loss of these chromosomes has been associated with better chemotherapeutic response and prolonged overall survival. Loss of chromosome 22 is a well defined abnormality in ependymomas. In addition, deletion of chromosome 6 q may be another frequent chromosomic aberration in paediatric ependymomas.

Publication types

  • Review

MeSH terms

  • Brain Neoplasms / genetics*
  • Brain Neoplasms / pathology
  • Chromosomes / genetics
  • Chromosomes / ultrastructure
  • Ependymoma / genetics*
  • Ependymoma / pathology
  • Humans
  • Oligodendroglioma / genetics*
  • Oligodendroglioma / pathology