Histone deacetylase inhibitor (HDACI) PCI-24781 potentiates cytotoxic effects of doxorubicin in bone sarcoma cells

Cancer Chemother Pharmacol. 2011 Feb;67(2):439-46. doi: 10.1007/s00280-010-1344-7. Epub 2010 May 12.

Abstract

Purpose: To better understand the mechanisms of cytotoxicity and cell death induced by HDACI PCI-24781 in bone sarcoma cells.

Methods: Four bone sarcoma cell lines were treated with PCI-24781, and the cytotoxicity was investigated. Further, accumulation of acetylated histones, p21, and PARP cleavage were evaluated in PCI-24781-treated cells. The synergistic effect of PCI-24781 to doxorubicin and its mechanism was investigated in bone sarcoma cells.

Results: MTT assay demonstrated that the growth of bone sarcoma cells was inhibited after treatment with PCI-24781. Accumulation of acetylated histones, p21, and PARP cleavage were found in PCI-24781-treated cells. Expression of DNA repair protein RAD51 was inhibited, and the expression of apoptosis protein GADD45α was induced by PCI-24781 in bone sarcoma cells. Bone sarcoma cells treated with PCI-24781 become more sensitive to doxorubicin. The caspase-3/7 activity was increased with doxorubicin and PCI-24781 treatment in these cells.

Conclusions: HDACI PCI-24781 has a synergistic effect on doxorubicin-induced apoptosis in bone sarcoma cells.

Publication types

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

MeSH terms

  • Acetylation / drug effects
  • Apoptosis / drug effects
  • Benzofurans / pharmacology*
  • Caspases / metabolism
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Chondrosarcoma / drug therapy*
  • Chondrosarcoma / metabolism
  • Doxorubicin / pharmacology*
  • Drug Synergism
  • Histone Deacetylase Inhibitors / pharmacology*
  • Histones / metabolism
  • Humans
  • Hydroxamic Acids / pharmacology*
  • Nuclear Proteins / metabolism
  • Osteosarcoma / drug therapy*
  • Osteosarcoma / metabolism
  • Rad51 Recombinase / metabolism

Substances

  • Benzofurans
  • Cell Cycle Proteins
  • GADD45A protein, human
  • Histone Deacetylase Inhibitors
  • Histones
  • Hydroxamic Acids
  • Nuclear Proteins
  • Doxorubicin
  • RAD51 protein, human
  • Rad51 Recombinase
  • Caspases
  • abexinostat