Restoration of gap junctional intercellular communication by caffeic acid phenethyl ester (CAPE) in a ras-transformed rat liver epithelial cell line

Cancer Lett. 2000 Aug 31;157(1):31-8. doi: 10.1016/s0304-3835(00)00470-5.

Abstract

Caffeic acid phenethyl ester (CAPE), an active ingredient of honeybee propolis, has been identified as having anti-inflammatory, anti-viral and anti-cancer properties. Since the deficiency of gap junctional intercellular communication (GJIC) has been shown to be a characteristic of most cancer cells, this study was designed to test the hypothesis that the anti-carcinogenic activity of CAPE might be related to its ability to restore GJIC in tumorigenic GJIC-deficient cells (WB-ras2 cells). The results showed that CAPE restored GJIC, phosphorylation of connexin 43 (Cx43) and its normal localization on the plasma membrane in WB-ras2 cells after 3 days at 5 microg/ml concentration. Additionally, CAPE inhibited growth in soft agar and decreased the protein level of p21(ras). The results are consistent with the hypothesis that the anti-cancer mechanism of CAPE may be mediated by its ability to restore GJIC.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology*
  • Anticarcinogenic Agents / toxicity
  • Caffeic Acids / pharmacology*
  • Caffeic Acids / toxicity
  • Cell Adhesion / physiology
  • Cell Communication / drug effects*
  • Cell Communication / physiology
  • Cell Division / drug effects
  • Cell Division / physiology
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic / drug effects*
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / pathology
  • Connexin 43 / biosynthesis
  • Connexin 43 / metabolism
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Gap Junctions / drug effects*
  • Gap Junctions / physiology
  • Gene Expression / drug effects
  • Genes, ras / drug effects*
  • Genes, ras / physiology
  • Liver / cytology
  • Liver / drug effects*
  • Liver / metabolism
  • Oncogene Protein p21(ras) / biosynthesis
  • Oncogene Protein p21(ras) / genetics
  • Phenylethyl Alcohol / analogs & derivatives*
  • Phenylethyl Alcohol / pharmacology*
  • Phenylethyl Alcohol / toxicity
  • Phosphorylation / drug effects
  • Rats
  • Rats, Inbred F344
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Anticarcinogenic Agents
  • Caffeic Acids
  • Connexin 43
  • Oncogene Protein p21(ras)
  • caffeic acid phenethyl ester
  • Phenylethyl Alcohol