Selective small-molecule inhibitors as chemical tools to define the roles of matrix metalloproteinases in disease

被引:24
作者
Meisel, Jayda E. [1 ]
Chang, Mayland [1 ]
机构
[1] Univ Notre Dame, 354C McCourtney Hall, Notre Dame, IN 46556 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2017年 / 1864卷 / 11期
关键词
Matrix metalloproteinases; Gelatinases; Thiiranes; ND-322; ND-336; MMP roles; BLOOD-BRAIN-BARRIER; LONG-TERM PROGNOSIS; GELATINASE INHIBITOR; INFLAMMATORY ARTHRITIS; FUNCTIONAL RECOVERY; TISSUE INHIBITOR; MICE DEFICIENT; TETHERED RESIN; FOOT ULCERS; CANCER;
D O I
10.1016/j.bbamcr.2017.04.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The focus of this article is to highlight novel inhibitors and current examples where the use of selective small molecule inhibitors has been critical in defining the roles of matrix metalloproteinases (MMPs) in disease. Selective small-molecule inhibitors are surgical chemical tools that can inhibit the targeted enzyme; they are the method of choice to ascertain the roles of MMPs and complement studies with knockout animals. This strategy can identify targets for therapeutic development as exemplified by the use of selective small-molecule MMP inhibitors in diabetic wound healing, spinal cord injury, stroke, traumatic brain injury, cancer metastasis, and viral infection. This article is part of a Special Issue entitled: Matrix Metalloproteinases edited by Rafael Fridman.
引用
收藏
页码:2001 / 2014
页数:14
相关论文
共 131 条
[1]
[Anonymous], 2011, J Spinal Cord Med, V34, P620, DOI 10.1179/204577211X13218754005537
[2]
[Anonymous], 2015, UND CAUS DEATH 1999
[3]
LONG-TERM PROGNOSIS FOR DIABETIC-PATIENTS WITH FOOT ULCERS [J].
APELQVIST, J ;
LARSSON, J ;
AGARDH, CD .
JOURNAL OF INTERNAL MEDICINE, 1993, 233 (06) :485-491
[4]
Armstrong David G, 2007, Int Wound J, V4, P286
[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]
Structural Bases for Substrate and Inhibitor Recognition by Matrix Metalloproteinases [J].
Aureli, Loretta ;
Gioia, Magda ;
Cerbara, Ilaria ;
Monaco, Susanna ;
Fasciglione, Giovanni Francesco ;
Marini, Stefano ;
Ascenzi, Paolo ;
Topai, Alessandra ;
Coletta, Massimo .
CURRENT MEDICINAL CHEMISTRY, 2008, 15 (22) :2192-2222
[7]
MT5-MMP is a new pro-amyloidogenic proteinase that promotes amyloid pathology and cognitive decline in a transgenic mouse model of Alzheimer's disease [J].
Baranger, Kevin ;
Marchalant, Yannick ;
Bonnet, Amandine E. ;
Crouzin, Nadine ;
Carrete, Alex ;
Paumier, Jean-Michel ;
Py, Nathalie A. ;
Bernard, Anne ;
Bauer, Charlotte ;
Charrat, Eliane ;
Moschke, Katrin ;
Seiki, Mothoharu ;
Vignes, Michel ;
Lichtenthaler, Stefan F. ;
Checler, Frederic ;
Khrestchatisky, Michel ;
Rivera, Santiago .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2016, 73 (01) :217-236
[8]
STIMULATION OF INVITRO HUMAN SKIN COLLAGENASE EXPRESSION BY PLATELET-DERIVED GROWTH-FACTOR [J].
BAUER, EA ;
COOPER, TW ;
HUANG, JS ;
ALTMAN, J ;
DEUEL, TF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (12) :4132-4136
[9]
Apolipoprotein E controls cerebrovascular integrity via cyclophilin A [J].
Bell, Robert D. ;
Winkler, Ethan A. ;
Singh, Itender ;
Sagare, Abhay P. ;
Deane, Rashid ;
Wu, Zhenhua ;
Holtzman, David M. ;
Betsholtz, Christer ;
Armulik, Annika ;
Sallstrom, Jan ;
Berk, Bradford C. ;
Zlokovic, Berislav V. .
NATURE, 2012, 485 (7399) :512-516
[10]
MMP-9 and MMP-2 Contribute to Neuronal Cell Death in iPSC Models of Frontotemporal Dementia with MAPT Mutations [J].
Biswas, Md Helal U. ;
Almeida, Sandra ;
Lopez-Gonzalez, Rodrigo ;
Mao, Wenjie ;
Zhang, Zhijun ;
Karydas, Anna ;
Geschwind, Michael D. ;
Biernat, Jacek ;
Mandelkow, Eva-Maria ;
Futai, Kensuke ;
Miller, Bruce L. ;
Gao, Fen-Biao .
STEM CELL REPORTS, 2016, 7 (03) :316-324