Differential expression of growth factors in squamous cell carcinoma and precancerous lesions of the lung

Clin Cancer Res. 2002 Mar;8(3):734-44.

Abstract

Purpose: This study was conducted to evaluate the clinical significance of the localization of epidermal growth factor receptor (EGF-r), transforming growth factor (TGF)-alpha, and erbB-2 in the development, progression and prognosis of squamous cell cancers (SCCs) of the lung.

Experimental design: The localization of EGF-r, TGF-alpha, and erbB-2 was evaluated immunohistochemically in 60 archival specimens of SCC of the lung and in 60 lung specimens without cancer. To clarify the patterns of expression of EGF-r in these tumors, the patterns of expression of EGF-r in cells in culture were monitored after challenging normal human bronchial epithelial and SCC cell lines with either EGF or TGF-alpha at physiological concentrations.

Results and conclusions: The expression of EGF-r, erbB-2, and TGF-alpha were significantly higher in SCC and associated precancerous lesions than in the normal bronchial epithelium and hyperplastic lesions of noncancer specimens. A statistically significant stepwise increase in expression from uninvolved bronchial epithelium to precancerous lesions to SCC was observed with EGF-r and TGF-alpha. The localization of EGF-r in the cytoplasm (P = 0.04), but not in the membrane (P = 0.20), of SCCs was significantly associated with poor overall survival of subjects. To demonstrate the biological relevance of cytoplasmic expression of EGF-r, we noted that there was a prompt reduction in the membrane expression and a concomitant increase in cytoplasmic expression of EGF-r after adding either EGF or TGF-alpha to the cell culture medium. Overall, the study identified an involvement of EGF-r and TGF-alpha in the development of SCCs. The prognostic importance of EGF-r expression in the cytoplasm of lung cancer probably is an indication of the prognostic importance of trafficking of the EGF-r receptor between the Golgi apparatus and cell membranes and of internalization of EGF-r after an interaction with one of the EGF-r ligands at the cellular membrane surface.

Publication types

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

MeSH terms

  • Carcinoma, Squamous Cell / metabolism*
  • Carcinoma, Squamous Cell / pathology
  • Cell Membrane
  • Cytoplasm / physiology
  • Epithelial Cells / pathology
  • ErbB Receptors / metabolism*
  • Humans
  • Hyperplasia / metabolism
  • Hyperplasia / pathology
  • Immunoenzyme Techniques
  • Ligands
  • Lung Neoplasms / metabolism*
  • Lung Neoplasms / pathology
  • Precancerous Conditions / metabolism*
  • Precancerous Conditions / pathology
  • Prognosis
  • Receptor, ErbB-2 / metabolism*
  • Survival Rate
  • Transforming Growth Factor alpha / metabolism*
  • Tumor Cells, Cultured / metabolism*
  • Tumor Cells, Cultured / pathology

Substances

  • Ligands
  • Transforming Growth Factor alpha
  • ErbB Receptors
  • Receptor, ErbB-2