N-myc is an essential downstream effector of Shh signaling during both normal and neoplastic cerebellar growth

Cancer Res. 2006 Sep 1;66(17):8655-61. doi: 10.1158/0008-5472.CAN-06-1621.

Abstract

We examined the genetic requirements for the Myc family of oncogenes in normal Sonic hedgehog (Shh)-mediated cerebellar granule neuronal precursor (GNP) expansion and in Shh pathway-induced medulloblastoma formation. In GNP-enriched cultures derived from N-myc(Fl/Fl) and c-myc(Fl/Fl) mice, disruption of N-myc, but not c-myc, inhibited the proliferative response to Shh. Conditional deletion of c-myc revealed that, although it is necessary for the general regulation of brain growth, it is less important for cerebellar development and GNP expansion than N-myc. In vivo analysis of compound mutants carrying the conditional N-myc null and the activated Smoothened (ND2:SmoA1) alleles showed, that although granule cells expressing the ND2:SmoA1 transgene are present in the N-myc null cerebellum, no hyperproliferation or tumor formation was detected. Taken together, these findings provide in vivo evidence that N-myc acts downstream of Shh/Smo signaling during GNP proliferation and that N-myc is required for medulloblastoma genesis even in the presence of constitutively active signaling from the Shh pathway.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division
  • Cerebellar Neoplasms / genetics*
  • Cerebellar Neoplasms / pathology
  • Cerebellum / cytology*
  • Cerebellum / pathology
  • Child
  • Genes, myc*
  • Hedgehog Proteins / physiology*
  • Humans
  • Kinetics
  • Medulloblastoma / genetics*
  • Medulloblastoma / pathology
  • Mice
  • Mice, Knockout
  • Proto-Oncogene Proteins c-myc / deficiency
  • Proto-Oncogene Proteins c-myc / genetics
  • Signal Transduction

Substances

  • Hedgehog Proteins
  • Proto-Oncogene Proteins c-myc
  • SHH protein, human
  • Shh protein, mouse