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From the Department of Surgery, University of South Florida, Tampa, Florida.
Correspondence: Address correspondence and reprint requests to: Alexander S. Rosemurgy II, MD, Department of Surgery, University of South Florida, PO Box 1289, Room F-145, Tampa, FL 33601; Fax: 813-844-7396; E-mail: arosemur{at}hsc.usf.edu
Abstract: Matrix metalloproteinases (MMPs) have received much attention in recent years for their role in a variety of malignancies. Pancreatic cancer is no exception; MMP-2 and MMP-9 show high levels of expression in clinical and experimental models. Inhibition of MMPs has shown great promise with synthetic inhibitors, such as BB-94, as tumorostatic agents in preclinical models, particularly when these are combined with gemcitabine. These findings have led to several clinical trials using the MMP inhibitors Marimastat and BAY12-9566. Herein, we discuss the roles of MMPs and their inhibition in pancreatic cancer.
Key Words: Pancreatic cancer Matrix metalloproteinase MMP TIMP
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