Emerging translational approaches to target STAT3 signalling and its impact on vascular disease

Cardiovasc Res. 2015 Jun 1;106(3):365-74. doi: 10.1093/cvr/cvv103. Epub 2015 Mar 17.

Abstract

Acute and chronic inflammation responses characterize the vascular remodelling processes in atherosclerosis, restenosis, pulmonary arterial hypertension, and angiogenesis. The functional and phenotypic changes in diverse vascular cell types are mediated by complex signalling cascades that initiate and control genetic reprogramming. The signalling molecule's signal transducer and activator of transcription 3 (STAT3) plays a key role in the initiation and continuation of these pathophysiological changes. This review highlights the pivotal involvement of STAT3 in pathological vascular remodelling processes and discusses potential translational therapies, which target STAT3 signalling, to prevent and treat cardiovascular diseases. Moreover, current clinical trials using highly effective and selective inhibitors of STAT3 signalling for distinct diseases, such as myelofibrosis and rheumatoid arthritis, are discussed with regard to their vascular (side-) effects and their potential to pave the way for a direct use of these molecules for the prevention or treatment of vascular diseases.

Keywords: Angiogenesis; Atherosclerosis; Restenosis; Signal transducer and activator of transcription 3; Translational medicine.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cardiovascular Agents / therapeutic use*
  • Drug Discovery*
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Humans
  • Molecular Targeted Therapy*
  • Neovascularization, Physiologic / drug effects
  • Regeneration / drug effects
  • STAT3 Transcription Factor / antagonists & inhibitors*
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / drug effects*
  • Translational Research, Biomedical*
  • Vascular Diseases / drug therapy*
  • Vascular Diseases / metabolism
  • Vascular Diseases / pathology
  • Vascular Diseases / physiopathology

Substances

  • Cardiovascular Agents
  • STAT3 Transcription Factor