High expression of Met/hepatocyte growth factor receptor suppresses tumorigenicity in NCI-H1264 lung carcinoma cells

Christine To, Isolde Seiden, Ni Liu, Dennis Wigle, Ming Sound Tsao

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

The protein product of c-met proto-oncogene, Met, is a tyrosine kinase receptor for the hepatocyte growth factor (HGF). Met receptor is expressed in normal human bronchial epithelium. In comparison, its expression in squamous cell carcinoma (SQCC) of the lung is markedly decreased in a great majority of cases. To understand further the role of Met receptor overexpression in non-small-cell lung carcinoma, we forced-expressed the full-length met cDNA in the NCI-H1264 (H1264) lung carcinoma cell line with low constitutive expression of this receptor. In vitro studies demonstrated that increased Met expression in H1264 cells resulted in strong inhibition of their ability to form soft agar colonies and in marked suppression of tumorigenicity in the subcutaneous tissue of immune-deficient mice. This is despite inconsistent alteration in the proliferation rate on plastic surfaces. Tumor cells explanted from occasional xenograft tumors formed by the Met-overexpressing H1264 cells also demonstrated marked down-regulation of the receptor protein levels as compared to the transplanted cells. The results suggest that constitutive overexpression of Met receptor may negatively regulate the malignancy of certain human lung cancer cells.

Original languageEnglish (US)
Pages (from-to)45-53
Number of pages9
JournalExperimental Cell Research
Volume273
Issue number1
DOIs
StatePublished - Jan 1 2002

Keywords

  • Hepatocyte growth factor
  • Lung cancer
  • Met
  • Scatter factor
  • Squamous cell carcinoma
  • Tumor suppression

ASJC Scopus subject areas

  • Cell Biology

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