Regulation of focal adhesion-associated protein tyrosine kinase by both cellular adhesion and oncogenic transformation

Nature. 1992 Aug 20;358(6388):690-2. doi: 10.1038/358690a0.


Increasing evidence indicates that the integrin family of cell adhesion receptors can transduce biochemical signals from the extracellular matrix to the cell interior to modulate cell growth and differentiation. We have shown that integrin/ligand interactions can trigger tyrosine phosphorylation of a protein of M(r) 120,000 (pp120), so it is possible that signal transduction by integrins might involve activation of intracellular protein tyrosine kinases as an early event in cell binding to the extracellular matrix. Here we report that pp120 is identical to the focal adhesion-associated protein tyrosine kinase pp125FAK (refs 3, 4). We show that tyrosine phosphorylation of this protein is modulated both by cell adhesion and transformation by pp60v-src, and that these changes in phosphorylation are correlated with increased pp125FAK tyrosine kinase activity. A model is proposed to relate these findings to the molecular basis of anchorage-independent growth of transformed cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3T3 Cells
  • Animals
  • Cell Adhesion*
  • Cell Line
  • Cell Transformation, Viral*
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Immunologic Techniques
  • In Vitro Techniques
  • Integrins / metabolism
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Oncogene Protein pp60(v-src) / metabolism
  • Phosphorylation
  • Phosphotyrosine
  • Protein-Tyrosine Kinases / immunology
  • Protein-Tyrosine Kinases / metabolism*
  • Signal Transduction
  • Tyrosine / analogs & derivatives
  • Tyrosine / metabolism


  • Integrins
  • Membrane Glycoproteins
  • Phosphotyrosine
  • Tyrosine
  • Protein-Tyrosine Kinases
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Oncogene Protein pp60(v-src)
  • Ptk2 protein, mouse