Hydroxydibenzoylmethane induces apoptosis through repressing ornithine decarboxylase in human promyelocytic leukemia HL-60 cells

Exp Mol Med. 2011 Apr 30;43(4):189-96. doi: 10.3858/emm.2011.43.4.023.

Abstract

Ornithine decarboxylase (ODC) is the rate-limiting enzyme in polyamine biosynthesis and a target for chemoprevention. Hydroxydibenzoylmethane (HDB), a derivative of dibenzoylmethane of licorice, is a promising chemopreventive agent. In this paper, we investigated whether HDB would inhibit the ODC pathway to enhance apoptosis in human promyelocytic leukemia HL-60 cells. We found ODC enzyme activity was reduced during HDB treatment. Overexpression of ODC in HL-60 parental cells could reduce HDB-induced apoptosis, which leads to loss of mitochondrial membrane potential (Δψ(m)), through lessening intracellular ROS. Furthermore, ODC overexpression protected cytochrome c release and the activation of caspase-3 following HDB treatment. The results demonstrated HDB-induced apoptosis was through a mechanism of down-regulation of ODC and occurred along a ROS-dependent mitochondria-mediated pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Caspase 3 / metabolism
  • Chalcones / metabolism
  • Chalcones / pharmacology*
  • Chemoprevention
  • Cytochromes c / biosynthesis
  • Cytochromes c / metabolism
  • Down-Regulation
  • Gene Expression
  • HL-60 Cells
  • Humans
  • Immunoblotting
  • Leukemia, Myeloid / enzymology*
  • Leukemia, Myeloid / pathology
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / enzymology
  • Ornithine Decarboxylase / genetics
  • Ornithine Decarboxylase / metabolism*
  • Ornithine Decarboxylase Inhibitors
  • Reactive Oxygen Species / analysis
  • Reactive Oxygen Species / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Chalcones
  • Ornithine Decarboxylase Inhibitors
  • Reactive Oxygen Species
  • hydroxydibenzoylmethane
  • Cytochromes c
  • Caspase 3
  • Ornithine Decarboxylase