Matrix metalloproteinases

被引:247
作者
Johnson, LL [1 ]
Dyer, R [1 ]
Hupe, DJ [1 ]
机构
[1] Warner Lambert Co, Parke Davis Pharmaceut Res, Dept Biochem, Ann Arbor, MI 48105 USA
关键词
D O I
10.1016/S1367-5931(98)80122-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix metalloproteinases are a family of highly regulated peptidases that are collectively responsible for the degradation of extracellular matrix during tissue remodeling. Dysregulated activity has long been implicated in the pathologies of cancer and arthritis, and the number of diseases more recently associated with these enzymes has been increasing. In the past year, new transgenic models of matrix metalloproteinase knockouts have been described, allowing the direct assessment of specific enzyme activity in particular disease models. In addition, more selective inhibitors with improved pharmacokinetic profiles have entered clinical trials, allowing the assessment of the safety and efficacy of this strategy.
引用
收藏
页码:466 / 471
页数:6
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共 52 条
  • [1] Matrix metalloproteinase inhibitors 1998
    Beckett, RP
    Whittaker, M
    [J]. EXPERT OPINION ON THERAPEUTIC PATENTS, 1998, 8 (03) : 259 - 282
  • [2] Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alpha v beta 3
    Brooks, PC
    Stromblad, S
    Sanders, LC
    vonSchalscha, TL
    Aimes, RT
    StetlerStevenson, WG
    Quigley, JP
    Cheresh, DA
    [J]. CELL, 1996, 85 (05) : 683 - 693
  • [3] MATRILYSIN-INHIBITOR COMPLEXES - COMMON THEMES AMONG METALLOPROTEASES
    BROWNER, MF
    SMITH, WW
    CASTELHANO, AL
    [J]. BIOCHEMISTRY, 1995, 34 (20) : 6602 - 6610
  • [4] Metalloproteinase inhibitors and the prevention of connective tissue breakdown
    Cawston, TE
    [J]. PHARMACOLOGY & THERAPEUTICS, 1996, 70 (03) : 163 - 182
  • [5] Matrix metalloproteinases, tumor necrosis factor and multiple sclerosis: An overview
    Chandler, S
    Miller, KM
    Clements, JM
    Lury, J
    Corkill, D
    Anthony, DCC
    Adams, SE
    Gearing, AJH
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1997, 72 (02) : 155 - 161
  • [6] Matrix metalloproteinase expression during experimental autoimmune encephalomyelitis and effects of a combined matrix metalloproteinase and tumour necrosis factor-alpha inhibitor
    Clements, JM
    Cossins, JA
    Wells, GMA
    Corkill, DJ
    Helfrich, K
    Wood, LM
    Pigott, R
    Stabler, G
    Ward, GA
    Gearing, AJH
    Miller, KM
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1997, 74 (1-2) : 85 - 94
  • [7] X-ray structure of a hydroxamate inhibitor complex of stromelysin catalytic domain and its comparison with members of the zinc metalloproteinase superfamily
    Dhanaraj, V
    Ye, QZ
    Johnson, LL
    Hupe, DJ
    Ortwine, DF
    Dubar, JB
    Rubin, JR
    Pavlovsky, A
    Humblet, C
    Blundell, TL
    [J]. STRUCTURE, 1996, 4 (04) : 375 - 386
  • [8] MATRIX METALLOPROTEINASES AND CARDIOVASCULAR-DISEASE
    DOLLERY, CM
    MCEWAN, JR
    HENNEY, AM
    [J]. CIRCULATION RESEARCH, 1995, 77 (05) : 863 - 868
  • [9] Influence of hypercholesterolemia and adventitial inflammation on the development of aortic aneurysm in rabbits
    Freestone, T
    Turner, RJ
    Higman, DJ
    Lever, MJ
    Powell, JT
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (01) : 10 - 17
  • [10] REVERSAL OF EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS WITH A HYDROXAMATE INHIBITOR OF MATRIX METALLOPROTEASES
    GIJBELS, K
    GALARDY, RE
    STEINMAN, L
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) : 2177 - 2182