Activation of PKC-alpha is required for migration of C6 glioma cells

Acta Neurobiol Exp (Wars). 2010;70(3):239-45. doi: 10.55782/ane-2010-1795.

Abstract

The PKC signaling pathway has been implicated in diverse cellular functions. Here, we sought to investigate the role of PKC-alpha÷beta in C6 glioma cell migration. We found that both PKC-alpha and PKC-beta were expressed by C6 glioma cells, but only PKC-alpha was markedly activated in serum-treated C6 cells. Go6976, a PKC-alpha÷beta specific inhibitor, was found to cause a dose-dependent reduction of PKC-alpha activation and cell migration induced by serum in C6 cells. These results collectively indicated that the PKC-alpha signaling pathway is necessary for glioma cell migration. Our findings may provide an insight into a better understanding to the malignant progression of gliomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimetabolites
  • Blotting, Western
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology
  • Bromodeoxyuridine
  • Cell Line, Tumor
  • Cell Movement / physiology*
  • Enzyme Activation
  • Glioma / metabolism
  • Glioma / pathology
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Protein Kinase C-alpha / antagonists & inhibitors
  • Protein Kinase C-alpha / metabolism*
  • Protein Kinase Inhibitors / pharmacology
  • Rats

Substances

  • Antimetabolites
  • Protein Kinase Inhibitors
  • Protein Kinase C-alpha
  • Bromodeoxyuridine