Integrin-TGF-beta crosstalk in fibrosis, cancer and wound healing

EMBO Rep. 2010 Feb;11(2):97-105. doi: 10.1038/embor.2009.276. Epub 2010 Jan 15.

Abstract

Accumulating evidence indicates that there is extensive crosstalk between integrins and TGF-beta signalling. TGF-beta affects integrin-mediated cell adhesion and migration by regulating the expression of integrins, their ligands and integrin-associated proteins. Conversely, several integrins directly control TGF-beta activation. In addition, a number of integrins can interfere with both Smad-dependent and Smad-independent TGF-beta signalling in different ways, including the regulation of the expression of TGF-beta signalling pathway components, the physical association of integrins with TGF-beta receptors and the modulation of downstream effectors. Reciprocal TGF-beta-integrin signalling is implicated in normal physiology, as well as in a variety of pathological processes including systemic sclerosis, idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease and cancer; thus, integrins could provide attractive therapeutic targets to interfere with TGF-beta signalling in these processes.

Publication types

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

MeSH terms

  • Animals
  • Disease Progression
  • Fibrosis / etiology
  • Fibrosis / genetics
  • Fibrosis / metabolism
  • Humans
  • Integrins / metabolism
  • Integrins / physiology*
  • Models, Biological
  • Neoplasms / etiology*
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Receptor Cross-Talk / physiology*
  • Transforming Growth Factor beta / metabolism
  • Transforming Growth Factor beta / physiology*
  • Wound Healing / genetics
  • Wound Healing / physiology*

Substances

  • Integrins
  • Transforming Growth Factor beta