Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244059
Title: Identification of the transduction pathways mediating the cellular responses to the hepatocyte growth factor/scatter factor
Author: Bardelli, Alberto
ISNI:       0000 0001 3444 6543
Awarding Body: University of London
Current Institution: University College London (University of London)
Date of Award: 1996
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Abstract:
Hepatocyte Growth Factor (HGF) is a mesenchymal cytokine capable of inducing proliferation and motility (scattering) in epithelial cells. This dual biological response depends on the interaction of HGF with its receptor, the tyrosine kinase c-Met. Ligand-induced activation of the HGF receptor triggers a number of signaling pathways in target cells. Signaling by tyrosine kinase receptors is normally mediated by selective interaction between effectors containing src homology 2 (SH2) domains and specific phosphotyrosine residues in the activated receptor. The HGF receptor is characterized by a unique signal transduction mechanism involving a multi-functional docking site made of two tandemly arranged phosphotyrosines embedded in the degenerate sequence YVH/NV. Upon autophosphorylation, these tyrosines bind and concomitantly activate multiple SH2-containing transducers, including the Grb2/SOS complex, phosphatidylinositol 3-kinase (PI 3-kinase), phospholipase C-γ (PLC-γ) and pp60Src. These interactions are characterized by fast association and dissociation rates thus favoring a rapid exchange of effectors in vivo. The multi-functional docking site is strictly required for the receptor's transforming, scattering, invasive and metastatic ability. Signalling mutants of the multifunctional docking site indicate that preferential coupling of the receptor to either Ras or PI 3-kinase is sufficient to promote scattering, but impairs invasion and metastases. Conversely, concomitant activation of both pathways promotes transformation and invasion, and induces a fully metastatic phenotype. These results imply that HGF receptor-mediated motility, transformation, and invasion have distinct signalling requirements, and suggest that simultaneous activation of Ras and PI-3K is both necessary and sufficient for the HGF receptor invasive-metastatic potential. Altogether these data indicate that the multifunctional docking site represents the main transductional switch for the HGF receptor.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.244059  DOI: Not available
Keywords: HGF; Mesenchymal cytokine
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