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Histone deacetylase inhibitors: new drugs for the treatment of inflammatory diseases?
Author(s): Blanchard F, Chipoy C
Source: DRUG DISCOVERY TODAY    Volume: 10    Issue: 3    Pages: 197-204    Published: FEB 1 2005  
Times Cited: 65     References: 61     
Abstract: Histone deacetylase (HDAC) inhibitors induce cell cycle arrest and differentiation in cancer cells and have been in Phase I-II clinical trials for the treatment of various solid or haematological malignancies. In recent years, HDAC inhibitors have emerged as potent contenders for anti-inflammatory drugs, offering new lines of therapeutic intervention for rheumatoid arthritis or lupus erythematosus. The molecular mode of action of HDAC inhibitors is still controversial but seems to rely on reduced inflammatory mediator production, such as nitric oxide or cytokines, which implies inhibition of the transcription factor NF-kappaB. These anti-inflammatory effects will hopefully lead us to appreciate the complex anti-tumour effects of HDAC inhibitors.
Document Type: Review
Language: English
Reprint Address: Blanchard, F (reprint author), Univ Nantes, EA 3822, Lab Pathophysiol Bone Resorpt & Therapy Primit Bo, 1 Rue Gaston Veil, F-44035 Nantes 1, France
Addresses:
1. Univ Nantes, EA 3822, Lab Pathophysiol Bone Resorpt & Therapy Primit Bo, F-44035 Nantes 1, France
2. INSERM, ER17, F-44035 Nantes, France
Publisher: ELSEVIER SCI LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
Subject Category: Pharmacology & Pharmacy
IDS Number: 893CD
ISSN: 1359-6446
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