The role of matrix metalloproteinases in osteoarthritis pathogenesis: An updated review

被引:401
作者
Mehana, El-Sayed E. [1 ]
Khafaga, Asmaa F. [1 ]
El-Blehi, Samar S. [1 ]
机构
[1] Alexandria Univ, Fac Vet Med, Dept Pathol, Edfina 22758, Egypt
关键词
Osteoarthritis; Matrix metalloproteases; MMPs; MMP-13; MMP inhibitors; EXPRESSION; GENE; CARTILAGE; CLONING; COLLAGENASE; MATRILYSIN; CDNA; IDENTIFICATION; STROMELYSIN-3; ASSIGNMENT;
D O I
10.1016/j.lfs.2019.116786
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Extensive degeneration of articular cartilage (AC) is a primary event in the pathogenesis of osteoarthritis (OA) and other types of joint and bone inflammation. OA results in the loss of joint function, usually accompanied by severe pain, and are the most common type of arthritis, affecting more than 10% of adults. The characteristic signs of OA are progressive cartilage destruction and, eventually, complete loss of chondrocytes. A key enzyme responsible for these degenerative changes in cartilage is matrix metalloproteinase-13 (MMP-13), which is thought to be a major contributor to the degenerative process occurring during OA pathogenesis. The aim of the present review is to shed light on the general role of MMPs, with special emphasis on MMP-13, in the induction of OA and the general basis of OA treatment. The pathogenic mechanism of this highly prevalent disease is not clear, and no effective disease-modifying treatment is currently available. Any updated information about OA treatment in human patients will also benefit companion animals such as horses and dogs, which also suffer from OA. Selective inhibition of MMP-13 seems to be an attractive therapeutic strategy.
引用
收藏
页数:9
相关论文
共 67 条
[1]
Amy R. N., 2016, CLIN ONCOL, V18, P1135
[2]
Anne M. M., 2009, SEMIN CELL DEV BIOL, V19, P34
[3]
[Anonymous], 2017, ARTHRITIS RES THER
[4]
A New Class of Potent Matrix Metalloproteinase 13 Inhibitors for Potential Treatment of Osteoarthritis Evidence of Histologic and Clinical Efficacy Without Musculoskeletal Toxicity in Rat Models [J].
Baragi, Vijaykumar M. ;
Becher, Gabriel ;
Bendele, Alison M. ;
Biesinger, Ralf ;
Bluhm, Harald ;
Boer, Juergen ;
Deng, Hongbo ;
Dodd, Rory ;
Essers, Michael ;
Feuerstein, Tim ;
Gallagher, Brian M., Jr. ;
Gege, Christian ;
Hochguertel, Matthias ;
Hofmann, Michael ;
Jaworski, Andreas ;
Jin, Lixia ;
Kiely, Andrew ;
Korniski, Brian ;
Kroth, Heiko ;
Nix, Darrell ;
Nolte, Bert ;
Piecha, Dorothea ;
Powers, Timothy S. ;
Richter, Frank ;
Schneider, Matthias ;
Steeneck, Christoph ;
Sucholeiki, Irving ;
Taveras, Arthur ;
Timmermann, Andreas ;
Van Veldhuizen, Joshua ;
Weik, Juergen ;
Wu, Xinyuan ;
Xia, Bing .
ARTHRITIS AND RHEUMATISM, 2009, 60 (07) :2008-2018
[5]
HUMAN MACROPHAGE METALLOELASTASE - GENOMIC ORGANIZATION, CHROMOSOMAL LOCATION, GENE LINKAGE, AND TISSUE-SPECIFIC EXPRESSION [J].
BELAAOUAJ, A ;
SHIPLEY, JM ;
KOBAYASHI, DK ;
ZIMONJIC, DB ;
POPESCU, N ;
SILVERMAN, GA ;
SHAPIRO, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14568-14575
[6]
PROTEOLYTIC REMODELING OF EXTRACELLULAR-MATRIX [J].
BIRKEDALHANSEN, H .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) :728-735
[7]
Remodelling the extracellular matrix in development and disease [J].
Bonnans, Caroline ;
Chou, Jonathan ;
Werb, Zena .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2014, 15 (12) :786-801
[8]
Boulay A, 2001, CANCER RES, V61, P2189
[9]
MOLECULAR-CLONING OF HUMAN SYNOVIAL CELL COLLAGENASE AND SELECTION OF A SINGLE GENE FROM GENOMIC DNA [J].
BRINCKERHOFF, CE ;
RUBY, PL ;
AUSTIN, SD ;
FINI, ME ;
WHITE, HD .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (02) :542-546