Numbl inhibits glioma cell migration and invasion by suppressing TRAF5-mediated NF-κB activation

Mol Biol Cell. 2012 Jul;23(14):2635-44. doi: 10.1091/mbc.E11-09-0805. Epub 2012 May 16.

Abstract

The Notch signaling regulator Numblike (Numbl) is expressed in the brain, but little is known regarding its role in the pathophysiology of glial cells. In this paper, we report that Numbl expression was down-regulated in high-grade human glioma tissue samples and glioblastoma cell lines. To investigate the role of Numbl in glioma migration and invasion, we generated human glioma cell lines in which Numbl was either overexpressed or depleted. Overexpression of Numbl suppressed, while elimination of Numbl promoted, the migration and invasion of glioma cells. Numbl inhibited glioma migration and invasion by dampening NF-κB activity. Furthermore, Numbl interacted directly with tumor necrosis factor receptor-associated factor 5 (TRAF5), which signals upstream and is required for the activation of NF-κB, and committed it to proteasomal degradation by promoting K48-linked polyubiquitination of TRAF5. In conclusion, our data suggest that Numbl negative regulates glioma cell migration and invasion by abrogating TRAF5-induced activation of NF-κB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain / metabolism
  • Brain / pathology
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Gene Expression Regulation, Neoplastic
  • Glioblastoma / metabolism
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • NF-kappa B / metabolism*
  • Neoplasm Invasiveness / genetics
  • Signal Transduction / genetics
  • TNF Receptor-Associated Factor 5 / metabolism*
  • Ubiquitination

Substances

  • Intracellular Signaling Peptides and Proteins
  • NF-kappa B
  • NUMBL protein, human
  • TNF Receptor-Associated Factor 5