Induction of apoptosis and inhibition of telomerase activity by trichostatin A, a histone deacetylase inhibitor, in human leukemic U937 cells

Exp Mol Pathol. 2007 Feb;82(1):77-84. doi: 10.1016/j.yexmp.2006.02.004. Epub 2006 Mar 30.

Abstract

The objective of the present study was to investigate the effect of trichostatin A (TSA), a histone deacetylase (HDAC) inhibitor, on the cell growth and apoptosis and its effect on the telomerase activity in human leukemic cell line U937. Exposure of U937 cells to TSA resulted in growth inhibition and induction of apoptosis in a dose-dependent manner as measured by hemocytometer counts, fluorescence microscopy, agarose gel electrophoresis and flow cytometry analysis. The increase in apoptosis was associated with the up-regulation in proapoptotic Bax expression and down-regulation of antiapoptotic Bcl-2 and Bcl-X(L). TSA treatment inhibited the levels of cIAP family members and induced the proteolytic activation of caspase-3, which was associated with concomitant degradation of poly(ADP-ribose)-polymerase and beta-catenin protein. TSA treatment markedly inhibited the activity of telomerase in a dose-dependent fashion. Additionally, the expression of human telomerase reverse transcriptase (hTERT), a main determinant of the telomerase enzymatic activity, was progressively down-regulated by TSA treatment. We therefore conclude that TSA demonstrated antiproliferative and apoptosis-inducing effects on U937 cells in vitro, and that changes in Bcl-2 family protein levels as well as telomerase activity may play an important role in its mechanism of action.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Blotting, Western
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cyclin D1 / drug effects
  • Dose-Response Relationship, Drug
  • Electrophoresis, Agar Gel
  • Enzyme Inhibitors / pharmacology*
  • Flow Cytometry
  • Histone Deacetylases / drug effects
  • Humans
  • Hydroxamic Acids / pharmacology*
  • Leukemia / enzymology*
  • Microscopy, Fluorescence
  • Reverse Transcriptase Polymerase Chain Reaction
  • Telomerase / drug effects*
  • Telomerase / metabolism

Substances

  • Enzyme Inhibitors
  • Hydroxamic Acids
  • Cyclin D1
  • trichostatin A
  • Telomerase
  • Histone Deacetylases