Proteome analysis suggests that mitochondrial dysfunction in stressed endothelial cells is reversed by a soy extract and isolated isoflavones

J Proteome Res. 2007 Jun;6(6):2132-42. doi: 10.1021/pr060547y. Epub 2007 May 16.

Abstract

Apoptosis is a driving force in atherosclerosis development. A soy extract or a combination of the soy isoflavones genistein and daidzein inhibited apoptosis induced by oxidized LDL in endothelial cells. Proteome analysis revealed that the LDL-induced alterations of numerous proteins were reversed by the extract and the genistein/daidzein mixture but only three protein entities, all functionally linked to mitochondrial dysfunction, were regulated in common by both treatments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Endothelial Cells / chemistry
  • Endothelial Cells / drug effects
  • Endothelial Cells / ultrastructure
  • Endothelium, Vascular / chemistry
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / ultrastructure
  • Genistein / pharmacology
  • Glycine max / chemistry*
  • Humans
  • Isoflavones / pharmacology*
  • Lipoproteins, LDL / antagonists & inhibitors*
  • Lipoproteins, LDL / toxicity
  • Mitochondria / chemistry
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Oxidation-Reduction
  • Plant Extracts / pharmacology
  • Proteome / analysis*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Isoflavones
  • Lipoproteins, LDL
  • Plant Extracts
  • Proteome
  • daidzein
  • Genistein