Combined inhibition of c-Src and epidermal growth factor receptor abrogates growth and invasion of head and neck squamous cell carcinoma

  • Priya Koppikar
  • , Seung Ho Choi
  • , Ann Marie Egloff
  • , Quan Cai
  • , Shinsuke Suzuki
  • , Maria Freilino
  • , Hiroshi Nozawa
  • , Sufi M. Thomas
  • , William E. Gooding
  • , Jill M. Siegfried
  • , Jennifer R. Grandis

Research output: Contribution to journalArticlepeer-review

96 Scopus citations

Abstract

Purpose: Increased expression and/or activation of epidermal growth factor receptor (EGFR) is associated with tumor progression and poor prognosis in many cancers, including head and neck squamous cell carcinoma (HNSCC). Src family kinases, including c-Src, mediate a variety of intracellular or extracellular signals that contribute to tumor formation and progression. This study was undertaken to elucidate the role of c-Src in the growth and invasion of HNSCC and to determine the effects of combined targeting of EGFR and Src kinases in HNSCC cell lines. Experimental Design: HNSCC ceils were engineered to stably express a dominant-active form of c-Src and investigated in cell growth and invasion assays. The biochemical effects of combined treatment with the Src inhibitor AZD0530, a potent, orally active Src inhibitor with Bcr/Abl activity, and the EGFR kinase inhibitor gefitinib were examined, as well as the consequences of dual Src/EGFR targeting on the growth and invasion of a panel of HNSCC cell lines. Results: HNSCC cells expressing dominant-active c-Src showed increased growth and invasion compared with vector-transfected controls. Combined treatment with AZD0530 and gefitinib resulted in greater inhibition of HNSCC cell growth and invasion compared with either agent alone. Conclusions: These results suggest that increased expression and activation of c-Src promotes HNSCC progression where combined targeting of EGFR and c-Src may be an efficacious treatment approach.

Original languageEnglish (US)
Pages (from-to)4284-4291
Number of pages8
JournalClinical Cancer Research
Volume14
Issue number13
DOIs
StatePublished - Jul 1 2008
Externally publishedYes

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