Molecular biology of pediatric gliomas

J Neurooncol. 1996 May-Jun;28(2-3):121-8. doi: 10.1007/BF00250194.

Abstract

The genes involved in the genesis and progression of adult astrocytic tumors have been an area of considerable investigation. The tumor suppressor gene, p53, has been implicated, as has the epidermal growth factor receptor gene. Additional currently unidentified genes lie on chromosomes 10 and 19. Interestingly, work on pediatric astrocytomas suggests that the genes involved are different. p53 is rarely mutated in pediatric tumors, the epidermal growth factor receptor gene is rarely amplified or mutated, and chromosome 10 deletions are rare. The only pediatric tumor that seems to mimic the findings in adult tumors is brainstem glioma, perhaps explaining the uniformly grim prognosis in this type of tumor. In the pilocytic astrocytoma of childhood, mutations in the neurofibromatosis type I gene have been implicated in tumor development. In this review, the oncogenesis of pediatric gliomas is discussed and compared and contrasted to what is known about tumors.

Publication types

  • Review

MeSH terms

  • Astrocytoma
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / pathology
  • Child
  • Cytogenetics
  • DNA, Neoplasm
  • Genes, Tumor Suppressor*
  • Glioma / genetics*
  • Glioma / pathology
  • Humans
  • Oncogenes

Substances

  • DNA, Neoplasm