For your first question
Both enzymes, are components of Epidermal growth factor receptor (EGFR) signalling pathway.
MMP is a matrix metalloproteinase, that triggers EGFR signalling, this can be done by a mechanism called transactivation
So, A signal from G-coupled receptor, or cytokine receptor could activate the cleavage of MMP, then MMP converts to a ligand for EGFR activation
For example Angiotensin II type 1 receptor (AT1R) and type 2 receptor (AT2R) which are GPCR, there are evidence for crosstalk with EGFR, look for this paper. This could be linked with hypertension or inflamation. Also cancer, could trigger EGFR receptors by NMP's.
And finally tissue inhibitors of metalloproteinases (TIMPs) are the negative regulator of MMP's
This are only an overview of the whole biological process involving MMP, so I think there is no single answer to your question, but you can delimit the topic for a specific disease, and look for papers at google scholar.
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