[Effect of valproic acid on apoptosis of leukemia HL-60 cells and expression of h-tert gene]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010 Dec;18(6):1445-50.
[Article in Chinese]

Abstract

This study was aimed to clarify whether valproic acid (VPA) induces apoptosis of leukemia HL-60 cell line and its possible mechanism. The effect of different concentrations and treatment time of VPA on HL-60 cell proliferation was assayed by cytotoxicity test (CCK-8 method) and fluorescence microscopy, and flow cytometry was used to detect cell apoptosis. The expressions of telomerase subunit h-tert mRNA and apoptosis-related protein as well as caspase-3 activity were detected by real time-quantitative PCR, Western blot and ELISA respectively. The results indicated that VPA inhibited proliferation of HL-60 cells and induced cell apoptosis in a dose dependent manner (r = -0.87). The expressions of anti-apoptotic protein BCL-2 and h-tert mRNA were significantly decreased while the pro-apoptotic protein BAX and caspase-3 activity increased after treatment with VPA. The apoptosis rate of HL-60 cell was negatively correlated with expression of h-tert mRNA. It is concluded that VPA can inhibit leukemia HL-60 cell proliferation and induce apoptosis. The VPA displays anti-leukemia activity possibly through reducing h-tert mRNA and BCL-2 protein expression, increasing BAX expression and activity of caspase-3.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Caspase 3 / metabolism
  • HL-60 Cells
  • Humans
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Telomerase / metabolism*
  • Valproic Acid / pharmacology*
  • bcl-2-Associated X Protein / metabolism

Substances

  • BAX protein, human
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Valproic Acid
  • TERT protein, human
  • Telomerase
  • CASP3 protein, human
  • Caspase 3