Abstract
Receptor tyrosine kinases are important in cell signal transduction and proliferation. Abnormal expression of tyrosine kinases often leads to malignant transformation. C-met is a tyrosine kinase receptor and its ligand is hepatocyte growth factor (HGF). HGF/c-met plays diverse roles in regulation of cell growth, shape and movement. Constitutively activated met, such as tpr-met, is a potent oncogene in vitro, but its carcinogenic role in vivo remains unclear. Our study demonstrates that expression of tpr-met leads to development of mammary tumors and other malignancies in transgenic mice, and suggests that deregulated met expression may be involved in mammary carcinogenesis.
Original language | English (US) |
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Pages (from-to) | 2872-2877 |
Number of pages | 6 |
Journal | Journal of Clinical Investigation |
Volume | 97 |
Issue number | 12 |
State | Published - Jun 15 1996 |
Externally published | Yes |
Keywords
- c-met
- carcinogenesis
- hepatocyte growth factor
- receptor tyrosine kinase
- sarcoma
ASJC Scopus subject areas
- Medicine(all)