Regulation of GST-MDA-7 toxicity in human glioblastoma cells by ERBB1, ERK1/2, PI3K, and JNK1-3 pathway signaling

Mol Cancer Ther. 2008 Feb;7(2):314-29. doi: 10.1158/1535-7163.MCT-07-2150.

Abstract

The present studies defined the biological effects of a GST fusion protein of melanoma differentiation-associated gene-7 (mda-7), GST-MDA-7 (1 and 30 nmol/L), on cell survival and cell signaling in primary human glioma cells in vitro. GST-MDA-7, in a dose- and time-dependent fashion killed glioma cells with diverse genetic characteristics; 1 nmol/L caused arrest without death, whereas 30 nmol/L caused arrest and killing after exposure. Combined inhibition of extracellular signal-regulated kinase 1/2 (ERK1/2) and AKT function was required to enhance 1 nmol/L GST-MDA-7 lethality in all cell types, whereas combined activation of MEK1 and AKT was required to suppress 30 nmol/L GST-MDA-7 lethality; both effects are mediated in part by modulating c-Jun NH(2)-terminal kinase (JNK) 1-3 activity. The geldanamycin 17AAG inhibited AKT and ERK1/2 in GBM cells and enhanced GST-MDA-7 lethality. JNK1-3 signaling promoted BAX activation and mitochondrial dysfunction. In GBM6 cells, GST-MDA-7 (30 nmol/L) transiently activated p38 mitogen-activated protein kinase, which was modestly protective against JNK1-3-induced toxicity, whereas GST-MDA-7 (300 nmol/L) caused prolonged intense p38 mitogen-activated protein kinase activation, which promoted cell death. In GBM12 cells that express full-length mutant activated ERBB1, inhibition of ERBB1 did not modify GST-MDA-7 lethality; however, in U118 established glioma cells, stable overexpression of wild-type ERBB1 and/or truncated active ERBB1vIII suppressed GST-MDA-7 lethality. Our data argue that combined inhibition of ERK1/2 and AKT function, regardless of genetic background, promotes MDA-7 lethality in human primary human glioma cells via JNK1-3 signaling and is likely to represent a more ubiquitous approach to enhancing MDA-7 toxicity in this cell type than inhibition of ERBB1 function.

Publication types

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

MeSH terms

  • Apoptosis / genetics*
  • Cell Survival
  • Cytotoxins / genetics
  • Cytotoxins / pharmacology
  • ErbB Receptors / physiology*
  • Glioblastoma / genetics
  • Glioblastoma / pathology*
  • Glutathione Transferase / genetics
  • Glutathione Transferase / pharmacology
  • Humans
  • Interleukins / genetics*
  • Interleukins / pharmacology
  • JNK Mitogen-Activated Protein Kinases / physiology*
  • Mitogen-Activated Protein Kinase 1 / physiology*
  • Mitogen-Activated Protein Kinase 10 / physiology
  • Mitogen-Activated Protein Kinase 3 / physiology*
  • Mitogen-Activated Protein Kinase 8 / physiology
  • Mitogen-Activated Protein Kinase 9 / physiology
  • Phosphatidylinositol 3-Kinases / physiology*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / pharmacology
  • Signal Transduction / physiology
  • Time Factors
  • Tumor Cells, Cultured

Substances

  • Cytotoxins
  • Interleukins
  • Recombinant Fusion Proteins
  • interleukin-24
  • Glutathione Transferase
  • Mitogen-Activated Protein Kinase 10
  • Phosphatidylinositol 3-Kinases
  • Mitogen-Activated Protein Kinase 9
  • ErbB Receptors
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinase 8