Dichotomy of the function of DDR1 in cells and disease progression

Biochim Biophys Acta Mol Cell Res. 2019 Nov;1866(11):118473. doi: 10.1016/j.bbamcr.2019.04.003. Epub 2019 Apr 5.

Abstract

Discoidin domain receptors DDR1 and DDR2 are collagen receptor tyrosine kinases that have many roles in tissue development and disease progression. Under physiological conditions, DDR1 is predominantly expressed in epithelial cells and functions to maintain cell differentiation and tissue homeostasis. A switch in expression from DDR1 to DDR2 occurs during epithelial-to-mesenchymal transition. However, opposite effects of DDR1 are reported to be involved in the progression of cancer and fibrotic diseases. Accumulating evidence suggests that DDR1 is involved in pro-metastasis and pro-survival signals. This review summarizes the roles of DDR1 in epithelial cell differentiation, cell migration, cancer progression and tissues fibrosis and highlights how the dichotomous functions of DDR1 may relevant to different cell types and statues. Elucidation of the underlying mechanism of the dichotomous functions of DDR1 will help to develop DDR1 as a therapeutic target.

Keywords: Cancer; Collagen; DDR1; EMT; Fibrosis; Integrin β1.

Publication types

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

MeSH terms

  • Cell Adhesion
  • Cell Differentiation / physiology*
  • Cell Movement / physiology*
  • Collagen
  • Discoidin Domain Receptor 1 / physiology*
  • Discoidin Domain Receptor 2
  • Disease Progression*
  • Epithelial Cells / metabolism
  • Epithelial-Mesenchymal Transition
  • Fibrosis / metabolism*
  • Humans
  • Integrin beta1
  • Neoplasm Metastasis
  • Neoplasms / metabolism*
  • Receptor Protein-Tyrosine Kinases

Substances

  • Integrin beta1
  • Collagen
  • Discoidin Domain Receptor 1
  • Discoidin Domain Receptor 2
  • Receptor Protein-Tyrosine Kinases