Literature DB >> 1368394

The matrix metalloproteinases and their natural inhibitors: prospects for treating degenerative tissue diseases.

A J Docherty1, J O'Connell, T Crabbe, S Angal, G Murphy.   

Abstract

Uncontrolled matrix metalloproteinase activity is thought to be a cause of the tissue damage observed in many disease processes. None of the drugs currently in use can prevent tissue destruction, and strategies for the development of synthetic inhibitors have been hampered by a poor understanding of the biochemistry of matrix metalloproteinases. Recent cDNA cloning efforts and characterization of recombinant human matrix metalloproteinases have permitted structure-function analysis of the enzymes and their inhibitors. Progress in this area should help indicate a route to rational strategies for designing lead therapeutic compounds.

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Year:  1992        PMID: 1368394     DOI: 10.1016/0167-7799(92)90214-g

Source DB:  PubMed          Journal:  Trends Biotechnol        ISSN: 0167-7799            Impact factor:   19.536


  32 in total

1.  The architecture of cancer.

Authors:  J Waxman; H Wasan
Journal:  BMJ       Date:  1992-11-28

2.  Transcriptional activation by p53 of the human type IV collagenase (gelatinase A or matrix metalloproteinase 2) promoter.

Authors:  J Bian; Y Sun
Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

3.  Pharmacokinetics and safety assessments of high-dose and 4-week treatment with S-3304, a novel matrix metalloproteinase inhibitor, in healthy volunteers.

Authors:  Timothy G K Mant; Daniel Bradford; Dipti M Amin; Jaya Pisupati; Yoshikazu Kambayashi; Yoshitaka Yano; Kazushige Tanaka; Takuko Yamada-Sawada
Journal:  Br J Clin Pharmacol       Date:  2006-10-31       Impact factor: 4.335

4.  Cloning of a novel membrane-linked metalloproteinase from human myeloma cells.

Authors:  N McKie; D J Dallas; T Edwards; J F Apperley; R G Russell; P I Croucher
Journal:  Biochem J       Date:  1996-09-01       Impact factor: 3.857

Review 5.  Molecular mechanisms for the conversion of zymogens to active proteolytic enzymes.

Authors:  A R Khan; M N James
Journal:  Protein Sci       Date:  1998-04       Impact factor: 6.725

6.  Expression of collagen, interstitial collagenase, and tissue inhibitor of metalloproteinases-1 in restenosis after carotid endarterectomy.

Authors:  S T Nikkari; R L Geary; T Hatsukami; M Ferguson; R Forough; C E Alpers; A W Clowes
Journal:  Am J Pathol       Date:  1996-03       Impact factor: 4.307

7.  Membrane-type matrix metalloproteinase (MT-MMP) gene is expressed in stromal cells of human colon, breast, and head and neck carcinomas.

Authors:  A Okada; J P Bellocq; N Rouyer; M P Chenard; M C Rio; P Chambon; P Basset
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

8.  Computational insights into the selectivity mechanism of APP-IP over matrix metalloproteinases.

Authors:  Lingling Geng; Jian Gao; Wei Cui; Yancheng Tang; Mingjuan Ji; Bozhen Chen
Journal:  J Comput Aided Mol Des       Date:  2012-12-09       Impact factor: 3.686

9.  Inhibition of metalloproteinase activity of rheumatoid arthritis synovial cells by a new inhibitor [BE16627B; L-N-(N-hydroxy-2-isobutylsuccinamoyl)-seryl-L-valine].

Authors:  K Naito; S Nakajima; N Kanbayashi; A Okuyama; M Goto
Journal:  Agents Actions       Date:  1993-07

10.  Characterization of structural determinants and molecular mechanisms involved in pro-stromelysin-3 activation by 4-aminophenylmercuric acetate and furin-type convertases.

Authors:  M Santavicca; A Noel; H Angliker; I Stoll; J P Segain; P Anglard; M Chretien; N Seidah; P Basset
Journal:  Biochem J       Date:  1996-05-01       Impact factor: 3.857

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