The Met/HGF receptor is over-expressed in human osteosarcomas and is activated by either a paracrine or an autocrine circuit
- PMID: 7862451
The Met/HGF receptor is over-expressed in human osteosarcomas and is activated by either a paracrine or an autocrine circuit
Abstract
The c-MET oncogene encodes the receptor for the Hepatocyte Growth Factor/Scatter Factor (HGF), a cytokine that stimulates the invasive growth of normal and neoplastic cells. The Met/HGF receptor is expressed by epithelial cells and its ligand by cells of mesenchymal origin. Receptor-ligand interaction occurs via a paracrine circuit. We studied the expression of the Met/HGF receptor and of its ligand in mesenchymal human tumours by examining 39 clinical samples of bone tumours. The Met/HGF receptor was not detectable in the majority of bone tumours, as expected from their mesenchymal origin. Notably, the receptor was overexpressed in 60% of the osteosarcomas examined. In 12 osteosarcoma cell lines the Met/HGF receptor was overexpressed, phosphorylated by HGF stimulation and fully functional. HGF was detected in two out of seven clinical specimens of osteosarcoma. The ligand and the receptor are co-expressed in two clonal osteosarcoma cell lines. In these lines the Met/HGF receptor was constitutively phosphorylated; phosphorylation was suppressed by suramin treatment, a known blocker of autocrine loops. These data suggest that activation of the Met/HGF receptor by a paracrine or an autocrine mechanism might play a role in the particularly aggressive behaviour of osteosarcomas.
Similar articles
-
Expression of hepatocyte growth factor and the proto-oncogenic receptor c-Met in canine osteosarcoma.Vet Pathol. 2009 Sep;46(5):869-77. doi: 10.1354/vp.08-VP-0155-F-FL. Epub 2009 May 9. Vet Pathol. 2009. PMID: 19429984
-
Identification of a hepatocyte growth factor autocrine loop in a murine mammary carcinoma.Cell Growth Differ. 1996 Feb;7(2):263-70. Cell Growth Differ. 1996. PMID: 8822210
-
Expression of Met/hepatocyte growth factor receptor gene and malignant behavior of musculoskeletal tumors.Am J Pathol. 1996 Oct;149(4):1209-19. Am J Pathol. 1996. PMID: 8863670 Free PMC article.
-
Structure, biosynthesis and biochemical properties of the HGF receptor in normal and malignant cells.EXS. 1993;65:131-65. EXS. 1993. PMID: 8380735 Review.
-
The hepatocyte growth factor and its receptor.Stem Cells. 1993 Jul;11 Suppl 2:22-30. doi: 10.1002/stem.5530110805. Stem Cells. 1993. PMID: 8401259 Review.
Cited by
-
In the clinic: ongoing clinical trials evaluating c-MET-inhibiting drugs.Ther Adv Med Oncol. 2011 Nov;3(1 Suppl):S37-50. doi: 10.1177/1758834011423403. Ther Adv Med Oncol. 2011. PMID: 22128287 Free PMC article.
-
MicroRNAs signatures, bioinformatics analysis of miRNAs, miRNA mimics and antagonists, and miRNA therapeutics in osteosarcoma.Cancer Cell Int. 2020 Jun 17;20:254. doi: 10.1186/s12935-020-01342-4. eCollection 2020. Cancer Cell Int. 2020. PMID: 32565738 Free PMC article. Review.
-
Constitutively active c-Met kinase in PC-3 cells is autocrine-independent and can be blocked by the Met kinase inhibitor BMS-777607.BMC Cancer. 2012 May 28;12:198. doi: 10.1186/1471-2407-12-198. BMC Cancer. 2012. PMID: 22639908 Free PMC article.
-
Oncogenic mutants of RON and MET receptor tyrosine kinases cause activation of the beta-catenin pathway.Mol Cell Biol. 2001 Sep;21(17):5857-68. doi: 10.1128/MCB.21.17.5857-5868.2001. Mol Cell Biol. 2001. PMID: 11486025 Free PMC article.
-
Systemic treatment of soft-tissue sarcoma-gold standard and novel therapies.Nat Rev Clin Oncol. 2014 Apr;11(4):187-202. doi: 10.1038/nrclinonc.2014.26. Epub 2014 Mar 18. Nat Rev Clin Oncol. 2014. PMID: 24642677 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Medical
Miscellaneous