Bisacurone inhibits adhesion of inflammatory monocytes or cancer cells to endothelial cells through down-regulation of VCAM-1 expression

Int Immunopharmacol. 2008 Sep;8(9):1272-81. doi: 10.1016/j.intimp.2008.05.006. Epub 2008 Jun 9.

Abstract

Bisacurone, one of the active compounds of the traditionally used indigenous herb Curcuma longa Linne (Zingiberaceae), has anti-oxidant, anti-inflammatory, and anti-metastatic activities. We studied how the level of vascular cell adhesion molecule-1 (VCAM-1), one of the key molecules in the development of atherosclerosis as well as carcinogenesis and metastasis, might be affected by bisacurone in tumor necrosis factor-alpha (TNF-alpha)-activated human umbilical vein endothelial cells (HUVECs). Bisacurone dose-dependently inhibited TNF-alpha-mediated expression of VCAM-1. It showed significant suppressive effect on ROS generation in response to TNF-alpha stimulation and it blocked nuclear factor-kappa B (NF-kappaB) p65 translocation into the nucleus and phosphorylation of inhibitory factor kappaBalpha (IkappaBalpha). It also inhibited phosphorylation of Akt and PKC, which are upstream in the regulation of VCAM-1 by TNF-alpha. Furthermore, bisacurone decreased U937 monocyte and human oral cancer cell (Hep-2, QLL-I, SCC-15) adhesion to HUVECs stimulated by TNF-alpha, suggesting that it may inhibit the binding of these cells by regulating the expression of critical adhesion molecules by TNF-alpha. Thus, bisacurone may be beneficial in the treatment of inflammatory diseases, such as atherosclerosis, where inflammatory monocytes are involved in their pathology, and, moreover, in the development of tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Blotting, Western
  • Cell Adhesion / drug effects
  • Cells, Cultured
  • Cyclohexanols / pharmacology*
  • Down-Regulation / drug effects
  • Endothelial Cells / metabolism*
  • Endothelial Cells / pathology*
  • Extracellular Signal-Regulated MAP Kinases / biosynthesis
  • Extracellular Signal-Regulated MAP Kinases / genetics
  • Genes, Reporter
  • Humans
  • Inflammation / metabolism*
  • Inflammation / pathology*
  • Luciferases / genetics
  • Monocytes / drug effects*
  • Oncogene Protein v-akt / biosynthesis
  • Oncogene Protein v-akt / genetics
  • Oxidants / metabolism
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Plasmids / genetics
  • Protein Kinase C / biosynthesis
  • Protein Kinase C / genetics
  • Sesquiterpenes / pharmacology*
  • Transfection
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / pharmacology
  • Vascular Cell Adhesion Molecule-1 / biosynthesis*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclohexanols
  • Oxidants
  • Plant Extracts
  • Sesquiterpenes
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1
  • bisacurone
  • Luciferases
  • Oncogene Protein v-akt
  • Protein Kinase C
  • Extracellular Signal-Regulated MAP Kinases