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Overexpression and activation of hepatocyte growth factor/scatter factor in human non-small-cell lung carcinomas

Olivero, Martina and Rizzo, M. and Madeddu, Roberto Beniamino and Casadio, C. and Pennacchietti, Selma and Nicotra, M.R. and Prat, M. and Maggi, N. and Arena, Nicolò and Natali, Pier Giorgio and Comoglio, Paolo Maria and Di Renzo, Maria Flavia (1996) Overexpression and activation of hepatocyte growth factor/scatter factor in human non-small-cell lung carcinomas. British Journal of Cancer, Vol. 74 (12), p. 1862-1868. eISSN 1532-1827. Article.

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Hepatocyte growth factor/scatter factor (HGF/SF) stimulates the invasive growth of epithelial cells via the c-MET oncogene-encoded receptor. In normal lung, both the receptor and the ligand are detected, and the latter is known to be a mitogenic and a motogenic factor for both cultured bronchial epithelial cells and non-small-cell carcinoma lines. Here, ligand and receptor expression was examined in 42 samples of primary human non-small-cell lung carcinoma of different histotype. Each carcinoma sample was compared with adjacent normal lung tissue. The Met/HGF receptor was found to be 2 to 10-fold increased in 25% of carcinoma samples (P = 0.0113). The ligand, HGF/SF, was found to be 10 to 100-fold overexpressed in carcinoma samples (P < 0.0001). Notably, while HGF/SF was occasionally detectable and found exclusively as a single-chain inactive precursor in normal tissues, it was constantly in the biologically-active heterodimeric form in carcinomas. Immunohistochemical staining showed homogeneous expression of both the receptor and the ligand in carcinoma samples, whereas staining was barely detectable in their normal counterparts. These data show that HGF/SF is overexpressed and consistently activated in non-small-cell lung carcinomas and may contribute to the invasive growth of lung cancer.

Item Type:Article
ID Code:7299
Uncontrolled Keywords:Hepatocyte growth factor/scatter factor, non-small-cell lung cancer, human cancer, Met receptor
Subjects:Area 05 - Scienze biologiche > BIO/17 Istologia
Divisions:001 Università di Sassari > 01 Dipartimenti > Scienze biomediche
Publisher:Nature Publishing Group
Copyright Holders:© Stockton Press
Deposited On:29 Mar 2012 14:31

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