Telomere 3' overhang-specific DNA oligonucleotides induce autophagy in malignant glioma cells

FASEB J. 2007 Sep;21(11):2918-30. doi: 10.1096/fj.06-6941com. Epub 2007 Apr 20.

Abstract

Telomere 3' overhang-specific DNA oligonucleotides (T-oligos) induce cell death in cancer cells, presumably by mimicking telomere loop disruption. Therefore, T-oligos are considered an exciting new therapeutic strategy. The purpose of this study was to elucidate how T-oligos exert antitumor effects on human malignant glioma cells in vitro and in vivo. We demonstrated that T-oligos inhibited the proliferation of malignant glioma cells through induction of nonapoptotic cell death and mitochondria hyperpolarization, whereas normal astrocytes were resistant to T-oligos. Tumor cells treated with T-oligos developed features compatible with autophagy, with development of autophagic vacuoles and conversion of an autophagy-related protein, microtubule-associated protein 1 light chain 3 from type I (cytoplasmic form) to type II (membrane form of autophagic vacuoles). A reverse-phase protein microarray analysis and Western blotting revealed that treatment with T-oligos inhibited the mammalian target of the rapamycin (mTOR) and the signal transducer and activator of transcription 3 (STAT3). Moreover, pretreatment with T-oligos significantly prolonged the survival time of mice inoculated intracranially with malignant glioma cells compared with that of untreated mice and those treated with control oligonucleotides (P=0.0065 and P=0.043, respectively). These results indicate that T-oligos stimulate the induction of nonapoptotic autophagic also known as type II programmed cell death and are thus promising in the treatment of malignant glioma.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis
  • Astrocytes / metabolism
  • Autophagy*
  • Blotting, Western
  • Brain Neoplasms / genetics
  • Brain Neoplasms / pathology
  • Brain Neoplasms / therapy*
  • Cell Survival
  • Cells, Cultured
  • DNA / pharmacology*
  • Female
  • Flow Cytometry
  • Glioma / genetics
  • Glioma / pathology
  • Glioma / therapy*
  • Humans
  • Membrane Potential, Mitochondrial
  • Mice
  • Mice, Nude
  • Microtubule-Associated Proteins
  • Mitochondria / metabolism
  • Oligonucleotides / pharmacology*
  • Protein Array Analysis
  • Protein Kinases / metabolism
  • STAT3 Transcription Factor / metabolism
  • Sirolimus / pharmacology
  • Survival Rate
  • TOR Serine-Threonine Kinases
  • Telomerase / metabolism
  • Telomere / genetics*
  • Telomere / metabolism

Substances

  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • Oligonucleotides
  • STAT3 Transcription Factor
  • DNA
  • Protein Kinases
  • MTOR protein, human
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • Telomerase
  • Sirolimus