“…[2][3][4] Physiologic processes affected by stromelysin-1 activity include cartilage repair, 5,6 uveoscleral outflow, 7 controlled inflammatory processes, 8 menstruation, 9 parturition, 10 cell adhesion, 11 wound repair, 11 and cell migration. 12 Increased activity of stromelysin-1 increases the pathogenicity of various conditions, including benign and malignant neoplasias, 1,13-16 diabetes mellitus, 17 viral meningitis, 18 coronary artery disease, 19,20 cutis laxa, 21 hepatic cirrhosis, 22 osteoarthritis, 23,24 rheumatoid arthritis, 25,26 Crohn' s disease, 27 glomerular nephritis disease, 28 infection with Epstein-Barr virus, 29 response to damage caused by UV radiation, 30 chronic ulcers, 31 and autoimmune diseases. 32 Neoplasms that express stromelysin-1 in humans include carcinomas of the breast, prostate, squamous epithelium, liver, and biliary system as well as melanoma and bone cancer.…”