[Inhibitory effect of trichostatin A on HepG2 cell proliferation and the mechanisms]

Nan Fang Yi Ke Da Xue Xue Bao. 2014 Jun;34(7):917-22.
[Article in Chinese]

Abstract

Objective: To investigate the inhibitory effect of trichostatin A (TSA) on the proliferation of HepG2 cells and explore the underlying mechanism.

Methods: HepG2 cells exposed to different concentrations of TSA for 24, 48, or 72 h were examined for cell growth inhibition using a cell counting kit, changes in cell cycle distribution with flow cytometry, cell apoptosis with annexin V-FTIC/PI double staining, and cell morphology changes under inverted microscope. The expressions of beta-catenin, HDAC1, HDAC3, H3K9, cyclinD1 and Bax proteins in the exposed cells were detected by Western blotting, and the expressions of HDAC1 and HDAC3 mRNAs by quantitative fluorescent PCR.

Results: Exposure to TSA caused significant dose- and time-dependent inhibition of HepG2 cell proliferation (P<0.05) and resulted in increased cell percentage in G0/G1 and G2/M phases and decreased cell percentage in S phase. The apoptotic index in the control group was (6.22 ± 0.25)%, which increased to (7.17 ± 0.20)% and (18.14 ± 0.42)% after exposure to 250 and 500 nmol/L TSA, respectively. Exposure to 250 and 500 nmol/L TSA also caused cell morphology changes with numerous floating cells. The expressions of beta-catenin, H3K9 and Bax proteins were significantly increased and CyclinD1, HDAC1, and HDAC3 protein expressions decreased in TSA-treated cells, but the expressions of HDAC1 and HDAC3 mRNAs showed no significant changes.

Conclusions: TSA can inhibit the proliferation of HepG2 cells and induce cell cycle arrest and apoptosis by inhibiting HDAC activity, promoting histone acetylation, and activating Wnt/beta-catenin signaling pathway.

MeSH terms

  • Acetylation
  • Apoptosis
  • Cell Cycle Checkpoints
  • Cell Proliferation / drug effects*
  • Cyclin D1 / metabolism
  • Hep G2 Cells / drug effects
  • Histone Deacetylase 1 / metabolism
  • Histone Deacetylases / metabolism
  • Histones / metabolism
  • Humans
  • Hydroxamic Acids / pharmacology*
  • Wnt Signaling Pathway
  • bcl-2-Associated X Protein / metabolism
  • beta Catenin / metabolism

Substances

  • BAX protein, human
  • CCND1 protein, human
  • CTNNB1 protein, human
  • Histones
  • Hydroxamic Acids
  • bcl-2-Associated X Protein
  • beta Catenin
  • Cyclin D1
  • trichostatin A
  • HDAC1 protein, human
  • Histone Deacetylase 1
  • Histone Deacetylases
  • histone deacetylase 3