Overexpression of hepatocyte growth factor and its receptor c-Met in nasal polyps

Arch Otolaryngol Head Neck Surg. 2006 Sep;132(9):985-9. doi: 10.1001/archotol.132.9.985.

Abstract

Objectives: To investigate the expression and distribution of hepatocyte growth factor (HGF) and c-Met proteins in normal nasal mucosa and in nasal polyps and to evaluate the possible effects of HGF and c-Met on the development of nasal polyps.

Design: Prospective study.

Setting: Tertiary academic institution.

Patients: Normal inferior turbinate mucosa was obtained from 20 patients undergoing surgery for augmentation rhinoplasty. Nasal polyps were obtained from 20 patients undergoing endoscopic sinus surgery for chronic polypoid sinusitis.

Interventions: Semiquantitative reverse-transcriptase polymerase chain reaction, immunohistochemistry, and Western blot analysis were performed.

Main outcome measures: The expression and distribution of HGF and c-Met were analyzed.

Results: Using immunohistochemistry, moderate to high levels of HGF were mainly localized in submucosal glands of nasal polyps, while c-Met was detected in submucosal glands and in epithelial cells. In normal turbinate mucosa, immunopositive HGF was detected in submucosal glands, where faint staining was found, while c-Met was noted in epithelial cells and in submucosal glands. Semiquantitative reverse-transcriptase polymerase chain reaction and Western blot analysis showed that HGF expression was increased in nasal polyps compared with that in normal turbinate mucosa. The same result was observed for c-Met.

Conclusion: Elevated c-Met expression in combination with expression of HGF in nasal polyps may enhance the proliferation of epithelial cells and submucosal glandular cells through the release of HGF, which activates c-Met receptors in nasal polyps.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Gene Expression
  • Hepatocyte Growth Factor / metabolism*
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Nasal Mucosa / metabolism
  • Nasal Polyps / genetics
  • Nasal Polyps / metabolism*
  • Proto-Oncogene Proteins c-met / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Hepatocyte Growth Factor
  • Proto-Oncogene Proteins c-met