Key result
Extracellular proteases drive plaque growth, atherosclerosis, ACS, and restenosis, emerging as potential therapeutic targets.
Answers are grounded in this paper and cite their sources.
Extracellular proteolysis plays a key role in many pathophysiologic processes including cancer, inflammatory diseases, and cardiovascular conditions such as atherosclerosis and restenosis. Whereas matrix metalloproteinases are their best known member, many others are becoming better known. The extracellular proteases are a complex and heterogeneous superfamily of enzymes. They include metalloproteinases (matrix metalloproteinases, adamalysins, or pappalysins), serine proteases (elastase, coagulation factors, plasmin, tissue plasminogen activator, urokinase plasminogen activator), and the cysteine proteases (such cathepsins). In addition to their matrix degradation capabilities, they have other less well known biologic functions that include angiogenesis, growth factor bioavailability, cytokine modulation, receptor shedding, enhancing cell migration, proliferation, invasion, and apoptosis. This review discusses extracellular proteases relevant to the vasculature, their classification and function, and how protease disorders contribute to arterial plaque growth, including chronic atherosclerosis, acute coronary syndromes, restenosis, and vascular remodeling. These broad extracellular protease functions make them potentially interesting therapeutic targets.
No takes yet. Share an insight, caveat, or question.
García‐Touchard et al. (2005) conducted a review in Atherosclerosis and restenosis. Extracellular proteases was evaluated. Extracellular proteases contribute to arterial plaque growth, chronic atherosclerosis, acute coronary syndromes, and restenosis, making them potential therapeutic targets.
Synapse has enriched 10 related papers. Consider them for comparative context: