[The genetics of glioma: molecular classification]

Presse Med. 2004 Oct 23;33(18):1268-73. doi: 10.1016/s0755-4982(04)98905-1.
[Article in French]

Abstract

Gliomas result from specific genetic alterations--such as activation of specific oncogenes and/or inactivation of specific tumor suppressor genes. These alterations affect specific pathways involved in either signal transduction or cell cycle control, leading to phenotypic changes such as uncontrolled proliferation, inhibition of apoptosis, genetic instability, invasive properties. Tumoral progression includes multiple molecular pathways of clinical relevance: early alterations (p53 mutations for astrocytomas, 1p and 19q loss for oligodendrogliomas) and late alterations (EGF-R amplification, PTEN and P16/CDKN2A inactivation). Genetic profile is not only of diagnostic--but also prognostic relevance, as shown by 1p associated to 19q loss in oligodendrogliomas which is predictive of better prognosis and higher response rate.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Brain Neoplasms / classification*
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / physiopathology
  • Cell Cycle
  • Cell Transformation, Neoplastic / genetics
  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Genetic Markers*
  • Genetic Predisposition to Disease*
  • Glioma / classification*
  • Glioma / genetics*
  • Glioma / physiopathology
  • Humans
  • Prognosis
  • Signal Transduction

Substances

  • Genetic Markers