Histone Deacetylase Inhibitors for Treating a Spectrum of Diseases Not Related to Cancer

被引:134
作者
Dinarello, Charles A. [1 ,2 ]
Fossati, Gianluca [3 ]
Mascagni, Paolo [3 ]
机构
[1] Univ Colorado Denver, Dept Med, Div Infect Dis, Aurora, CO 80045 USA
[2] Radboud Univ Nijmegen, Med Ctr, Dept Med, NL-6525 ED Nijmegen, Netherlands
[3] Italfarmaco SpA, Res Ctr, Cinisello Balsamo, Italy
基金
美国国家卫生研究院;
关键词
SUBEROYLANILIDE HYDROXAMIC ACID; VERSUS-HOST-DISEASE; INTERLEUKIN-1 RECEPTOR ANTAGONIST; PROINFLAMMATORY GENE-EXPRESSION; COLLAGEN-INDUCED ARTHRITIS; VALPROIC ACID; HDAC INHIBITORS; TRICHOSTATIN-A; IN-VIVO; CELL-FUNCTION;
D O I
10.2119/molmed.2011.00116
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
This issue of Molecular Medicine contains 14 original research reports and state-of-the-art reviews on histone deacetylase n-hibitors (HDACi's), which are being studied in models of a broad range of diseases not related to the proapoptotic properties used to treat cancer. The spectrum of these diseases responsive to HDACi's is for the most part due to several antiinflamrnatory properties, often observed in vitro but importantly also in animal models. One unifying property is a reduction in cytokine production as well as inhibition of cytokine postreceptor signaling. Distinct from their use in cancer, the reduction in inflammation by HDACi's is consistently observed at low concentrations compared with the higher concentrations required for killing tumor cells. This characteristic makes HDACi's attractive candidates for treating chronic diseases, since low doses are well tolerated. For example, low oral doses of the HDACi givinostat have been used in children to reduce arthritis and are well tolerated. In addition to the antiinflammatory properties, HDACi's have shown promise in models of neurodegenerative disorders, and HDACi's also hold promise to drive HIV-1 out of latently infected cells. No one molecular mechanism accounts for the non-cancer-related properties of HDACi's, since there are 18 genes coding for histone deacetylases. Rather, there are mechanisms unique for the pathological process of specific cell types. In this overview, we summarize the preclinical data on HDACi's for therapy in a wide spectrum of diseases unrelated to the treatment of cancer. The data suggest the use of HDACi's in treating autoimmune as well as chronic inflammatory diseases. (C) 2011 The Feinstein Institute for Medical Research, www.feinsteininstitute.org Online address: http://www.molmed.org doi: 10.2119/molmed.2011.00116
引用
收藏
页码:333 / 352
页数:20
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