Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma

Cancer Genet Cytogenet. 1992 Jul 15;61(2):193-6. doi: 10.1016/0165-4608(92)90085-m.

Abstract

Although ependymomas comprise 5-10% of pediatric brain tumors, consistent cytogenetic aberrations have not been identified in these neoplasms. We report karyotypes for two ependymomas. A predominantly well-differentiated ependymoma contained several numerical chromosome aberrations, including monosomy 22. In contrast, an anaplastic ependymoma had a more complex karyotype that included loss of one chromosome 22 homologue and a balanced translocation at q13.3 in the remaining 22 homologue. These findings suggest the location of an ependymoma tumor suppressor gene on the long arm of chromosome 22.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Brain Neoplasms / genetics*
  • Cerebral Ventricle Neoplasms / genetics*
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 22*
  • Ependymoma / genetics*
  • Genes, Tumor Suppressor / genetics*
  • Humans
  • Male
  • Monosomy
  • Translocation, Genetic / genetics*