Effects of epidermal growth factor receptor and insulin-like growth factor 1 receptor inhibition on proliferation and intracellular signaling in cutaneous SCCHN: potential for dual inhibition as a therapeutic modality

Head Neck. 2013 Jan;35(1):86-93. doi: 10.1002/hed.22936. Epub 2012 Apr 12.

Abstract

Background: Combined inhibition of epidermal growth factor receptor (EGFR) and insulin-like growth factor-1 receptor (IGF-1R) has been proposed as a therapy for cutaneous squamous cell carcinoma of the head and neck (SCCHN).

Methods: Receptor expression and downstream signaling were assessed in cutaneous squamous cell carcinoma (SCC) cell lines and patient samples. EGFR and IGF-1R signaling was inhibited in cutaneous SCC cell lines using erlotinib and/or picropodophyllin.

Results: EGFR and IGF-1R were overexpressed in cutaneous SCCHN specimens relative to normal skin. Dual inhibition of both receptors prevented cell growth and decreased activation of Akt and p42/44 mitogen-activated protein kinase (MAPK) more effectively than either inhibitor alone.

Conclusion: Dual inhibition of EGFR and IGF-1R is effective at blocking cell growth, and is correlated with inhibition of Akt and p42/44 MAPK, suggesting that this may be a promising treatment for cutaneous SCCHN.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Squamous Cell / drug therapy*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Enzyme-Linked Immunosorbent Assay
  • ErbB Receptors / antagonists & inhibitors*
  • Erlotinib Hydrochloride
  • Fluorescent Antibody Technique
  • Head and Neck Neoplasms / drug therapy*
  • Humans
  • Insulin-Like Growth Factor Binding Protein 1 / antagonists & inhibitors*
  • Podophyllotoxin / analogs & derivatives
  • Podophyllotoxin / therapeutic use
  • Protein Kinase Inhibitors / therapeutic use
  • Quinazolines / therapeutic use
  • Signal Transduction
  • Squamous Cell Carcinoma of Head and Neck

Substances

  • Insulin-Like Growth Factor Binding Protein 1
  • Protein Kinase Inhibitors
  • Quinazolines
  • picropodophyllin
  • Erlotinib Hydrochloride
  • ErbB Receptors
  • Podophyllotoxin