Quest for selectivity in inhibition of matrix metalloproteinases

被引:59
作者
Brown, S
Meroueh, SO
Fridman, R
Mobashery, S
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[2] Wayne State Univ, Dept Pathol, Detroit, MI 48202 USA
关键词
D O I
10.2174/1568026043387854
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Matrix metalloproteinases (MMPs), of which at least 26 are known in humans, have been linked to a number of pathological conditions including tumor metastasis, inflammation, neurological and cardiovascular diseases. Inhibition of MMPs has been widely sought as a strategy in intervention of these disease processes. Whereas a large number of broad-spectrum MMP inhibitors have been developed over the past decade, these inhibitors have not met the promise and expectations in clinical trials. The broad-spectrum inhibition, which besides MMPs often targets other metalloproteinases, has been considered one of the potential problems that affects the therapeutic efficacy of MMPs inhibitors. Several MMP inhibitors that show selectivity for various MMPs have been reported in the past few years. This report describes the structural and inhibitory properties of these novel inhibitors, which hold considerable promise for effective targeting of these important enzymes.
引用
收藏
页码:1227 / 1238
页数:12
相关论文
共 96 条
[71]   Matrix metalloproteinases in lung biology [J].
Parks, WC ;
Shapiro, SD .
RESPIRATORY RESEARCH, 2001, 2 (01) :10-19
[72]   Cysteine array matrix metalloproteinase (CA-MMP)/MMP-23 is a type II transmembrane matrix metalloproteinase regulated by a single cleavage for both secretion and activation [J].
Pei, DQ ;
Kang, TB ;
Qi, HX .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) :33988-33997
[73]   CA-MMP: a matrix metalloproteinase with a novel cysteine array, but without the classic cysteine switch [J].
Pei, DQ .
FEBS LETTERS, 1999, 457 (02) :262-270
[74]   Low plasma levels of matrix metalloproteinase 9 permit increased tumor angiogenesis [J].
Pozzi, A ;
LeVine, WF ;
Gardner, HA .
ONCOGENE, 2002, 21 (02) :272-281
[75]   Glycosylation of natural human neutrophil gelatinase B and neutrophil gelatinase B-associated lipocalin [J].
Rudd, PM ;
Mattu, TS ;
Masure, S ;
Bratt, T ;
Van den Steen, PE ;
Wormald, MR ;
Küster, B ;
Harvey, DJ ;
Borregaard, N ;
Van Damme, J ;
Dwek, RA ;
Opdenakker, G .
BIOCHEMISTRY, 1999, 38 (42) :13937-13950
[76]   Encounter with unexpected collagenase-1 selective inhibitor: Switchover of inhibitor binding pocket induced by fluorine atom [J].
Sawa, M ;
Kondo, H ;
Nishimura, S .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (04) :581-584
[77]   Matrix metalloproteinase hypothesis of plaque rupture - Players keep piling up but questions remain [J].
Shah, PK ;
Galis, ZS .
CIRCULATION, 2001, 104 (16) :1878-1880
[78]   Metalloelastase is required for macrophage-mediated proteolysis and matrix invasion in mice [J].
Shipley, JM ;
Wesselschmidt, RL ;
Kobayashi, DK ;
Ley, TJ ;
Shapiro, SD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :3942-3946
[79]   The design, structure, and therapeutic application of matrix metalloproteinase inhibitors [J].
Skiles, JW ;
Gonnella, NC ;
Jeng, AY .
CURRENT MEDICINAL CHEMISTRY, 2001, 8 (04) :425-474
[80]  
STOCKER W, 1995, PROTEIN SCI, V4, P823