Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases

被引:655
作者
Hu, Jialiang
Van den Steen, Philippe E.
Sang, Qing-Xiang A.
Opdenakker, Ghislain
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
[2] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
关键词
D O I
10.1038/nrd2308
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Matrix metalloproteinases (MMPs) have outgrown the field of extracellular-matrix biology and have progressed towards being important regulatory molecules in cancer and inflammation. This rise in status was accompanied by the development of various classes of inhibitors. Although clinical trials with synthetic inhibitors for the treatment of cancer were disappointing, recent data indicate that the use of selective inhibitors might lead to new therapies for acute and chronic inflammatory and vascular diseases. In this Review, we compare the major classes of MMP inhibitors and advocate that future drug discovery should be based on crucial insights into the differential roles of specific MMPs in pathophysiology obtained with animal models, including knockout studies.
引用
收藏
页码:480 / 498
页数:19
相关论文
共 222 条
[1]   Urokinase-type plasminogen activator potentiates lipopolysaccharide-induced neutrophil activation [J].
Abraham, E ;
Gyetko, MR ;
Kuhn, K ;
Arcaroli, J ;
Strassheim, D ;
Park, JS ;
Shetty, S ;
Idell, S .
JOURNAL OF IMMUNOLOGY, 2003, 170 (11) :5644-5651
[2]   Chemically modified tetracyclines as inhibitors of matrix metalloproteinases [J].
Acharya, MR ;
Venitz, E ;
Figg, WD ;
Sparreboom, A .
DRUG RESISTANCE UPDATES, 2004, 7 (03) :195-208
[3]   Dystroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitis [J].
Agrawal, S ;
Anderson, P ;
Durbeej, M ;
van Rooijen, N ;
Ivars, F ;
Opdenakker, G ;
Sorokin, LM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (04) :1007-1019
[4]   Stromelysin-3 is a potent negative regulator of adipogenesis participating to cancer cell-adipocyte interaction/crosstalk at the tumor invasive front [J].
Andarawewa, KL ;
Motrescu, ER ;
Chenard, MP ;
Gansmuller, A ;
Stoll, I ;
Tomasetto, C ;
Rio, MC .
CANCER RESEARCH, 2005, 65 (23) :10862-10871
[5]   Role for matrix metalloproteinase 9 after focal cerebral ischemia, effects of gene knockout and enzyme inhibition with BB-94 [J].
Asahi, M ;
Asahi, K ;
Jung, JC ;
del Zoppo, GJ ;
Fini, ME ;
Lo, EH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (12) :1681-1689
[6]   Membrane-type 1 matrix metalloproteinase is required for normal alveolar development [J].
Atkinson, JJ ;
Holmbeck, K ;
Yamada, S ;
Birkedal-Hansen, H ;
Parks, WC ;
Senior, RM .
DEVELOPMENTAL DYNAMICS, 2005, 232 (04) :1079-1090
[7]   Molecular recognition of protein-ligand complexes: Applications to drug design [J].
Babine, RE ;
Bender, SL .
CHEMICAL REVIEWS, 1997, 97 (05) :1359-1472
[8]   Loss of collagenase-2 confers increased skin tumor susceptibility to male mice [J].
Balbín, M ;
Fueyo, A ;
Tester, AM ;
Pendás, AM ;
Pitiot, AS ;
Astudillo, A ;
Overall, CM ;
Shapiro, SD ;
López-Otín, C .
NATURE GENETICS, 2003, 35 (03) :252-257
[9]  
Barrett AJ, 2004, HDB PROTEOLYTIC ENZY
[10]   Elastin degradation and calcification in an abdominal aorta injury model - Role of matrix metalloproteinases [J].
Basalyga, DM ;
Simionescu, DT ;
Xiong, WF ;
Baxter, T ;
Starcher, BC ;
Vyavahare, NR .
CIRCULATION, 2004, 110 (22) :3480-3487