Abstract |
ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) proteinases have been implicated in a number of connective tissue pathologies including Ehlers-Danlos syndrome type VII C, Weill-Marchesani syndrome, encephalomyelitis, and arthritis. These proteinases therefore represent potential therapeutic targets for the treatment of such conditions. The synthesis and activity of ADAMTS proteinases is regulated at multiple levels: transcription, RNA splicing, translation, proteolytic processing, cofactor stimulation and inhibition, each of which represents a possible point of therapeutic intervention. Recent research suggests that, in addition to the direct inhibition of ADAMTS proteinases with low molecular weight non-peptidic inhibitors, targeting the transcription and protein processing of these enzymes could be effective therapeutic approaches.
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Authors | Gavin C Jones |
Journal | Current pharmaceutical biotechnology
(Curr Pharm Biotechnol)
Vol. 7
Issue 1
Pg. 25-31
(Feb 2006)
ISSN: 1389-2010 [Print] Netherlands |
PMID | 16472131
(Publication Type: Journal Article, Review)
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Chemical References |
- Protease Inhibitors
- ADAM Proteins
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Topics |
- ADAM Proteins
(antagonists & inhibitors, biosynthesis, genetics)
- Animals
- Connective Tissue Diseases
(drug therapy, enzymology)
- Humans
- Protease Inhibitors
(pharmacology, therapeutic use)
- Protein Processing, Post-Translational
- Transcription, Genetic
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