Combined Treatment of ATRA with Epigenetic Drugs Increases Aggressiveness of Glioma Xenografts

Anticancer Res. 2016 Apr;36(4):1489-96.

Abstract

Background/aim: Recently, anti-tumourigenic effects of all-trans-retinoic-acid (ATRA) on glioblastoma stem cells were demonstrated. Therefore we investigated if these beneficial effects could be enhanced by co-medication with epigenetic drugs such as the histone deacetylase (HDAC) inhibitor suberoylanilide hydroxamic acid (SAHA) or the DNA-methyltransferase inhibitor 5-aza-2'deoxycytidine (5-AZA).

Materials and methods: Glioma stem cell xenografts were treated for 42 days with ATRA plus SAHA or ATRA plus 5-AZA or the correspondent monotherapies. Tumour sizes, histological features, proliferation and apoptosis rates were assessed.

Results: Neither SAHA nor 5-AZA were able to enhance the anti-tumourigenic effect of ATRA. Instead, tumours became more aggressive. Combination of ATRA plus 5-AZA increased tumour size (p<0.05) and induced more frequent and larger necroses (p<0.05) and tumours were more invasive (p<0.05) in comparison to controls. A similar trend was observed for the combination of ATRA plus SAHA.

Conclusion: Combining ATRA with epigenetic drug therapies led to the unwanted opposite effect and increased aggressiveness of glioma xenografts, arguing against future clinical applications of such combinations.

Keywords: 5-AZA; ATRA; SAHA; stem-like glioma cells.

MeSH terms

  • Animals
  • Antimetabolites, Antineoplastic / adverse effects
  • Antimetabolites, Antineoplastic / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Azacitidine / adverse effects
  • Azacitidine / therapeutic use
  • Brain Neoplasms / drug therapy*
  • Brain Neoplasms / pathology
  • Cell Line, Tumor
  • Epigenomics
  • Female
  • Glioma / drug therapy*
  • Glioma / pathology
  • Histone Deacetylase Inhibitors / adverse effects
  • Histone Deacetylase Inhibitors / therapeutic use
  • Humans
  • Hydroxamic Acids / adverse effects
  • Hydroxamic Acids / therapeutic use
  • Mice, Inbred NOD
  • Mice, SCID
  • Tretinoin / adverse effects*
  • Tretinoin / therapeutic use
  • Tumor Burden / drug effects
  • Vorinostat
  • Xenograft Model Antitumor Assays

Substances

  • Antimetabolites, Antineoplastic
  • Histone Deacetylase Inhibitors
  • Hydroxamic Acids
  • Tretinoin
  • Vorinostat
  • Azacitidine