Anti-apoptotic effect of hepatocyte growth factor from actinomycin D in hepatocyte-derived HL7702 cells is associated with activation of PI3K/Akt signaling

Toxicol Lett. 2006 Aug 20;165(2):142-8. doi: 10.1016/j.toxlet.2006.02.006. Epub 2006 Apr 17.

Abstract

Actinomycin D (ActD) is a well-known cytotoxic chemotherapeutic reagent and the prevention of ActD-induced apoptotic cell death has been an attractive issue for biomedical investigators. Since phosphatidylinositol-3 kinase (PI3K)/Akt pathway is essential for cell survival, the present study has examined whether the preventive effect of hepatocyte growth factor (HGF) on ActD-induced apoptotic cell death in a human hepatocyte-derived cell line (HL7702) is associated with PI3K/Akt activation. Apoptotic cell death was measured by several methods including Hoechst 33342 staining, DNA fragmentation, and flow cytometry. We found that ActD caused a significant increase in apoptotic cell death, an effect significantly prevented by pre-addition of HGF in the cultures. HGF was found to significantly activate Akt phosphorylation while pre-treatment with PI3K specific inhibitor wortmannin further enhanced ActD-induced apoptotic effect, and also significantly prevented HGF's protection against ActD-induced apoptosis. These results suggest that HGF's prevention of ActD-induced apoptotic cell death in HL7702 cells is associated with the activation of PI3K/Akt signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androstadienes / pharmacology
  • Apoptosis / drug effects*
  • Cell Line
  • DNA Fragmentation
  • Dactinomycin / toxicity*
  • Dose-Response Relationship, Drug
  • Drug Antagonism
  • Drug Combinations
  • Hepatocyte Growth Factor / pharmacology*
  • Hepatocytes / drug effects*
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Humans
  • Phosphatidylinositol 3-Kinases / biosynthesis*
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Synthesis Inhibitors / toxicity*
  • Signal Transduction
  • Wortmannin

Substances

  • Androstadienes
  • Drug Combinations
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Synthesis Inhibitors
  • Dactinomycin
  • Hepatocyte Growth Factor
  • Wortmannin