Expression of MATH1, a marker of cerebellar granule cell progenitors, identifies different medulloblastoma sub-types

Neurosci Lett. 2004 Nov 11;370(2-3):180-5. doi: 10.1016/j.neulet.2004.08.053.

Abstract

In order to look for genetic markers helpful for the biological risk stratification of medulloblastomas (MBs) we assayed by real-time PCR expression levels of the following genes: MATH1, encoding a critical transcription factor for the differentiation of cerebellar granular cells (CGCs); PEDF, that encodes a trophic factor for CGCs and is located in a region of frequent allelic imbalance in MBs; and BIRC5, encoding the antiapoptotic protein survivin, usually overexpressed in malignancies. Expression levels of TRKC, higher in MBs with a more favorable prognosis, were also studied. Twenty-three patients were considered: MATH1 expression was strong in 14/23 and undetectable in the others. PEDF was up-regulated in 8/23, TRKC in 9/23, and BIRC5 in 23/23. MATH1 expression was significantly correlated with adult age (p < 0.0001), tumor location in hemispheres rather than the vermis (p < 0.0004), and PEDF and TRKC up-regulation (p < 0.008 and p < 0.04, respectively). During development MATH1 is selectively expressed in the external germinal layer (EGL) of the cerebellum. Thus, MATH1 expression identifies a subgroup of MBs that derive from the EGL and arise during adult age into cerebellar hemispheres. MATH1 mRNA-positive MBs express high levels of PEDF and show a trend towards longer survival, in agreement with increased expression of TRKC. BIRC5 expression, which is strong in all MBs and absent in normal cerebellum, lacks any prognostic value but could be explored for selective targeting of therapeutic factors to MBs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Basic Helix-Loop-Helix Transcription Factors
  • Biomarkers
  • Cell Differentiation / physiology
  • Cerebellum / cytology*
  • Cerebellum / metabolism
  • Eye Proteins / genetics
  • Eye Proteins / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Male
  • Medulloblastoma / classification*
  • Medulloblastoma / metabolism
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Middle Aged
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism
  • Neurons / metabolism*
  • RNA, Messenger / biosynthesis
  • Receptor, trkC / genetics
  • Receptor, trkC / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Serpins / genetics
  • Serpins / metabolism
  • Stem Cells / metabolism*
  • Survivin
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Atoh1 protein, mouse
  • BIRC5 protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • Biomarkers
  • Eye Proteins
  • Inhibitor of Apoptosis Proteins
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Nerve Growth Factors
  • RNA, Messenger
  • Serpins
  • Survivin
  • Transcription Factors
  • pigment epithelium-derived factor
  • Receptor, trkC