Hypoxia promotes apoptosis of human neuroblastoma cell lines with enhanced N-myc expression

Biochem Biophys Res Commun. 2001 Feb 23;281(2):272-6. doi: 10.1006/bbrc.2001.4342.

Abstract

We have examined the effect of hypoxia and nutrient depletion on the growth of human neuroblastoma cells with normal or enhanced expression of the N-myc oncogene. The combination of both conditions reduced the growth of neuroblastoma cells with normal N-myc expression. However, this effect was much more pronounced in neuroblastoma cells with enhanced N-myc expression and eventually resulted in apoptosis, presumably by the up-regulation of CD95. Our data suggest that therapeutic induction of tumor hypoxia and nutrient depletion (for example, by anti-angiogenesis) could help to improve the outcome of patients with neuroblastomas carrying the prognostically unfavourable N-myc amplification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Apoptosis / genetics
  • Cell Cycle / drug effects
  • Cell Cycle / genetics
  • Cell Division / drug effects
  • Cell Division / genetics
  • Cell Hypoxia
  • Culture Media, Serum-Free / pharmacology
  • DNA, Recombinant
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic
  • Genetic Vectors / genetics
  • Humans
  • Neuroblastoma / genetics*
  • Neuroblastoma / metabolism
  • Neuroblastoma / pathology
  • Oxygen / pharmacology*
  • Proto-Oncogene Proteins c-myc / genetics*
  • Proto-Oncogene Proteins c-myc / metabolism
  • Time Factors
  • Transfection
  • Tumor Cells, Cultured
  • fas Receptor / analysis

Substances

  • Culture Media, Serum-Free
  • DNA, Recombinant
  • Proto-Oncogene Proteins c-myc
  • fas Receptor
  • Oxygen