Involvement of the hepatocyte growth factor/scatter factor receptor c-met and of Bcl-xL in the resistance of oropharyngeal cancer to ionizing radiation

Int J Cancer. 2001 Feb 20;96(1):41-54. doi: 10.1002/1097-0215(20010220)96:1<41::aid-ijc5>3.0.co;2-f.

Abstract

The activation of cytoplasmic signal transduction pathways by a number of growth factors and their tyrosine-kinase receptors, including hepatocyte growth factor/scatter factor (HGF/SF) and its receptor c-met, exerts an inhibitory influence on apoptosis induced by ionizing radiation in vitro. The clinical relevance of the aforementioned ligand-receptor pair, of Bcl-xL, which is targeted by HGF/SF/c-met signaling, and of Bcl-2, was assessed by evaluating their predictive and prognostic impact in a cohort of 97 patients with radically irradiated squamous cell cancers of the oropharynx. Immunohistochemical expression of c-met and Bcl-xL was correlated with decreased rates of complete remission of the primary tumor in both the univariate (c-met: P = 0.01; Bcl-xL: P = 0.001) and multivariate analyses. Expression of c-met was, moreover, a significant and independent predictor of impaired local failure-free survival (P = 0.003), disease-free survival (P = 0.003) and overall survival (p = 0.001). Bcl-2 expression was, on the other hand, associated with a favorable outcome, in terms of both local failure-free survival (P = 0.01) and overall survival (P = 0.001). In accordance with in vitro data, c-met and Bcl-xL appear to be involved in the resistance of oropharyngeal cancers to ionizing radiation, and may therefore represent attractive targets for radiosensitization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Apoptosis / radiation effects
  • Biopsy
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / mortality
  • Carcinoma, Squamous Cell / radiotherapy*
  • Cohort Studies
  • Cytoplasm / metabolism
  • Disease-Free Survival
  • Female
  • Hepatocyte Growth Factor / biosynthesis
  • Hepatocyte Growth Factor / physiology*
  • Humans
  • Immunohistochemistry
  • Ligands
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Oropharyngeal Neoplasms / metabolism
  • Oropharyngeal Neoplasms / mortality
  • Oropharyngeal Neoplasms / radiotherapy*
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2 / physiology*
  • Proto-Oncogene Proteins c-met / biosynthesis
  • Proto-Oncogene Proteins c-met / physiology*
  • Radiation Tolerance*
  • Radiation, Ionizing
  • Remission Induction
  • Signal Transduction
  • Time Factors
  • Treatment Outcome
  • bcl-X Protein

Substances

  • BCL2L1 protein, human
  • Ligands
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-X Protein
  • Hepatocyte Growth Factor
  • Proto-Oncogene Proteins c-met