Induction of apoptosis by the licochalcone E in endothelial cells via modulation of NF-kappaB and Bcl-2 Family

Biol Pharm Bull. 2007 Dec;30(12):2290-3. doi: 10.1248/bpb.30.2290.

Abstract

Licochalcones have a variety of biological properties including anti-tumor, anti-parasitic and anti-bacterial activities. Recently, a new retrochalcone (licochalcone E, Lico-E) was isolated from the roots of Glycyrrhiza inflata (Chem. Pharm. Bull., 53, 2005, Yoon et al.) by cytotoxicity-guided fractionation. This study examined whether or not Lico-E-induced endothelial cell death occurs through apoptosis, and investigated molecular mechanisms involved in this process. Lico-E was found to suppress ECV304 cell growth and induce apoptosis. The induction of apoptosis by Lico-E was confirmed by the ladder-patterned DNA fragmentation, the presence of cleaved and condensed nuclear chromatin and the increased number of annexin V-positive cells. Lico-E could effectively inhibit the constitutive NF-kappaB activation, as revealed by the electrophoretic mobility shift assay and NF-kappaB-dependent luciferase reporter study. In addition, the Lico-E treatment caused a change in the Bax/Bcl-2 ratio that favored apoptosis. These results suggest that Lico-E induces endothelial cell apoptosis by modulating NF-kappaB and the Bcl-2 family.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors*
  • Apoptosis / drug effects*
  • Benzimidazoles
  • Blotting, Western
  • Cell Line
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cell Survival / drug effects
  • Chalcones / pharmacology*
  • DNA Fragmentation / drug effects
  • Electrophoretic Mobility Shift Assay
  • Endothelial Cells / drug effects
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Genes, bcl-2 / genetics
  • Genes, bcl-2 / physiology*
  • Humans
  • NF-kappa B / genetics
  • NF-kappa B / physiology*

Substances

  • Angiogenesis Inhibitors
  • Benzimidazoles
  • Chalcones
  • NF-kappa B
  • licochalcone E
  • bisbenzimide ethoxide trihydrochloride