Data from Specific Cross-talk between Epidermal Growth Factor Receptor and Integrin α<sub>v</sub>β<sub>5</sub> Promotes Carcinoma Cell Invasion and Metastasis

Abstract

<div>Abstract<p>Tyrosine kinase receptors and integrins play essential roles in tumor cell invasion and metastasis. Previously, we showed that epidermal growth factor (EGF) stimulation of pancreatic carcinoma cells led to invasion and metastasis that was blocked by antagonists of integrin α<sub>v</sub>β<sub>5</sub>. Here, we show that EGF stimulates metastasis of carcinoma cells via a Src-dependent phosphorylation of p130 CAS leading to activation of Rap1, a small GTPase involved in integrin activation. Specifically, EGF receptor (EGFR)–induced Src activity leads to phosphorylation of a region within the CAS substrate domain, which is essential for Rap1 and α<sub>v</sub>β<sub>5</sub> activation. This pathway induces α<sub>v</sub>β<sub>5</sub>-mediated invasion and metastasis <i>in vivo</i> yet does not influence primary tumor growth or activation of other integrins on these cells. These findings show cross-talk between a tyrosine kinase receptor and an integrin involved in carcinoma cell invasion and metastasis and may explain in part how inhibitors of EGFR affect malignant disease. [Cancer Res 2009;69(4):1383–91]</p></div>