Growth inhibition and differentiation of C6 glioma cells on treatment with hmba

Cell Biol Int. 2001;25(7):621-7. doi: 10.1006/cbir.2000.0696.

Abstract

HMBA, a differentiation inducer belonging to the class of hybrid polar compounds, is known to induce terminal differentiation of a number of leukemic and solid tumour cell lines. In this report we have shown that HMBA markedly inhibits growth of C6 glioma cells at non-cytotoxic concentrations ranging from 2.5 m m to 10 m m in a dose-dependent manner. The growth inhibitory effect can be detected as early as 18--24 h. By the sixth day the growth inhibition decreases at all the concentrations tested. Treatment with HMBA results in an accumulation of C6 cells in G0/G1 phase along with a decrease in the number of cells in S phase. HMBA induces morphological differentiation of C6 cells and increases expression of glial fibriliary acidic protein (GFAP), a marker for mature astrocytes. HMBA induces c-fos and represses cycloheximide-induced c-jun and fra-1 expression. HMBA-induced growth inhibition of C6 cells is accompanied by a decrease in Cdk4 protein levels. However, HMBA fails to sustain low Cdk4 levels, which may be responsible for HMBA's failure to sustain the growth inhibitory effect.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetamides / pharmacology*
  • Antineoplastic Agents / pharmacology*
  • Brain Neoplasms / drug therapy*
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology
  • Cell Cycle
  • Cell Differentiation / drug effects
  • Cell Division / drug effects
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinases / metabolism
  • DNA, Neoplasm / analysis
  • Drug Screening Assays, Antitumor
  • Glioma / drug therapy*
  • Glioma / metabolism
  • Glioma / pathology
  • Proto-Oncogene Proteins c-fos / metabolism
  • Proto-Oncogene Proteins c-jun / metabolism
  • Proto-Oncogene Proteins*
  • Tumor Cells, Cultured

Substances

  • Acetamides
  • Antineoplastic Agents
  • DNA, Neoplasm
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • fos-related antigen 1
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinases
  • hexamethylene bisacetamide