Inhibition of TACE or amphiregulin for the Modulation of EGF Receptor Signal Transactivation
AssigneeMax-Planck-Gesellschaft zur Foerderung der Wissenschaften e.V.
InventorsAxel Ullrich, Andreas Gschwind, Stefan Hart
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Abstract
The present invention relates to the modulation of transactivation of receptor tyrosine kinases by G protein or G protein-coupled receptor (GPCR) mediated signal transduction in a cell or an organism comprising inhibiting the activity of the metalloprotease TACE/ADAM17 and/or the activity of the receptor tyrosine kinase ligand amphiregulin.
Claims22
A method for modulating transactivation of receptor tyrosine kinases by G-protein or G protein-coupled receptor mediated signal transduction in a cell comprising specifically inhibiting the activity of amphiregulin and optionally TACE/ADAM 17.
A method of making a pharmaceutical composition for prevention and or treatment of a disorder which is caused by or associated with a transactivation of receptor tyrosine kinases by G protein or G protein-coupled receptor mediated signal transduction in a cell comprising combining a therapeutically effective dose of an inhibitor that specifically inhibits the activity of amphiregulin and optionally TACE/ADAM17 with pharmaceutically acceptable carriers, diluents, and/or adjuvants.
A method for the prevention and or treatment of a disorder which is caused by or associated with a transactivation of receptor tyrosine kinases by G protein or G protein-coupled receptor mediated signal transduction comprising administering a subject in need thereof an effective amount of a specific inhibitor of amphiregulin and optionally a specific inhibitor of TACE/ADAM17.
A method for identifying modulators of receptor tyrosine kinase transactivation by G protein or G protein-coupled receptor mediated signal transduction, comprising determining if a test compound is capable of specifically inhibiting the activity of amphiregulin and optionally the activity of TACE/ADAM17.
Dependencies are inferred from the claim text.