Resistance to hypoxia-induced, BNIP3-mediated cell death contributes to an increase in a CD133-positive cell population in human glioblastomas in vitro

J Neuropathol Exp Neurol. 2012 Dec;71(12):1086-99. doi: 10.1097/NEN.0b013e3182772d83.

Abstract

In addition to intrinsic regulatory mechanisms, brain tumor stemlike cells (BTSCs), a small subpopulation of malignant glial tumor-derived cells, are influenced by environmental factors. Previous reports showed that lowering oxygen tension induced an increase of BTSCs expressing CD133 and other stem cell-related genes and more pronounced clonogenic capacity in vitro. We investigated the mechanisms responsible for hypoxia-dependent induction of CD133-positive BTSCs in glioblastomas. We confirmed that cultures exposed to lowered oxygen levels showed a severalfold increase of CD133-positive BTSCs. Both the increase of CD133-positive cells and deceleration of the growth kinetics were reversible after transfer to normoxic conditions. Exposure to hypoxia induced BNIP3 (BCL2/adenovirus E1B 19-kDa protein-interacting protein 3)-dependent apoptosis preferentially in CD133-negative cells. In contrast, CD133-positive cells proved to be more resistant to hypoxia-induced programmed cell death. Application of the demethylating agent 5'-azacitidine resulted in an increase of BNIP3 expression levels in CD133-positive cells. Thus, epigenetic modifications led to their better survival in lowered oxygen tension. Moreover, the, hypoxia-induced increase of CD133-positive cells was inhibited after 5'-azacitidine treatment. These results suggest the possible efficacy of a novel therapy for glioblastoma focused on eradication of BTSCs by modifications of epigenetic regulation of gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AC133 Antigen
  • Antigens, CD / metabolism*
  • Antimetabolites, Antineoplastic / pharmacology
  • Azacitidine / pharmacology
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology*
  • Cell Death / drug effects
  • Cell Death / physiology
  • Cell Hypoxia / drug effects
  • Cell Hypoxia / physiology*
  • Cell Line
  • Cell Proliferation / drug effects
  • Chromatin Immunoprecipitation / methods
  • DNA Methylation
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic / drug effects
  • Glioblastoma / metabolism
  • Glioblastoma / pathology*
  • Glycoproteins / metabolism*
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Peptides / metabolism*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Signal Transduction / drug effects
  • Transfection

Substances

  • AC133 Antigen
  • Antigens, CD
  • Antimetabolites, Antineoplastic
  • BNIP3 protein, human
  • Glycoproteins
  • Membrane Proteins
  • PROM1 protein, human
  • Peptides
  • Proto-Oncogene Proteins
  • Azacitidine