Histone deacetylase inhibitors: new drugs for the treatment of inflammatory diseases?

被引:209
作者
Blanchard, F
Chipoy, C
机构
[1] Univ Nantes, EA 3822, Lab Pathophysiol Bone Resorpt & Therapy Primit Bo, F-44035 Nantes 1, France
[2] INSERM, ER17, F-44035 Nantes, France
关键词
D O I
10.1016/S1359-6446(04)03309-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:197 / 204
页数:8
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