Proteasome inhibitors enhance endothelial thrombomodulin expression via induction of Krüppel-like transcription factors

Arterioscler Thromb Vasc Biol. 2009 Oct;29(10):1587-93. doi: 10.1161/ATVBAHA.109.191957. Epub 2009 Aug 6.

Abstract

Objective: Impairment of the thrombomodulin-protein C anticoagulant pathway has been implicated in pathological thrombosis associated with malignancy. Patients who receive proteasome inhibitors as part of their chemotherapeutic regimen appear to be at decreased risk for thromboembolic events. We investigated the effects of proteasome inhibitors on endothelial thrombomodulin expression and function.

Methods and results: Proteasome inhibitors as a class markedly induced the expression of thrombomodulin and enhanced the protein C activating capacity of endothelial cells. Thrombomodulin upregulation was independent of NF-kappaB signaling, a principal target of proteasome inhibitors, but was instead a direct consequence of increased expression of the Krüppel-like transcription factors, KLF2 and KLF4. These effects were confirmed in vivo, where systemic administration of a proteasome inhibitor enhanced thrombomodulin expression that was paralleled by changes in the expression of KLF2 and KLF4.

Conclusions: These findings identify a novel mechanism of action of proteasome inhibitors that may help to explain their clinically observed thromboprotective effects.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Boronic Acids / pharmacology*
  • Bortezomib
  • Cells, Cultured
  • Endothelial Cells / drug effects*
  • Endothelial Cells / metabolism
  • Humans
  • Kruppel-Like Factor 4
  • Kruppel-Like Transcription Factors / genetics
  • Kruppel-Like Transcription Factors / physiology*
  • Male
  • Mice
  • Mice, Inbred C3H
  • NF-kappa B / antagonists & inhibitors
  • Protease Inhibitors / pharmacology*
  • Proteasome Inhibitors*
  • Protein C / physiology
  • Pyrazines / pharmacology*
  • Thrombomodulin / genetics*
  • Thrombomodulin / physiology

Substances

  • Boronic Acids
  • KLF2 protein, human
  • KLF4 protein, human
  • Klf4 protein, mouse
  • Kruppel-Like Factor 4
  • Kruppel-Like Transcription Factors
  • NF-kappa B
  • Protease Inhibitors
  • Proteasome Inhibitors
  • Protein C
  • Pyrazines
  • Thrombomodulin
  • Bortezomib