Literature DB >> 21879448

Rationale for HDAC inhibitor therapy in autoimmunity and transplantation.

Wayne W Hancock1.   

Abstract

While there are currently more than 70 ongoing clinical trials of inhibitors of so-called classical HDACs (HDACi) as anticancer therapies, given their potency as antiproliferative and angiostatic agents, HDACi also have considerable therapeutic potential as anti-inflammatory and immunosuppressive drugs. The utility of HDACi as anti-inflammatory agents is dependent upon their proving safe and effective in experimental models. Current pan-HDACi compounds are not well suited to this role, given the broad distribution of target HDACs and their complex and multifaceted mechanisms of action. In contrast, the development of isoform-selective HDACi may provide important new tools for therapy in autoimmunity and transplantation. This chapter discusses which HDACs are worthwhile targets in inflammation and progress toward their therapeutic inhibition, including the use of HDAC subclass and isoform-selective HDACi to promote the functions of Foxp3+ T regulatory cells.

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Year:  2011        PMID: 21879448     DOI: 10.1007/978-3-642-21631-2_6

Source DB:  PubMed          Journal:  Handb Exp Pharmacol        ISSN: 0171-2004


  5 in total

1.  HDAC expression and activity is upregulated in diseased lupus-prone mice.

Authors:  Nicole L Regna; Miranda D Vieson; Alexander M Gojmerac; Xin M Luo; David L Caudell; Christopher M Reilly
Journal:  Int Immunopharmacol       Date:  2015-10-21       Impact factor: 4.932

Review 2.  Glucocorticoid sensitivity in health and disease.

Authors:  Rogier A Quax; Laura Manenschijn; Jan W Koper; Johanna M Hazes; Steven W J Lamberts; Elisabeth F C van Rossum; Richard A Feelders
Journal:  Nat Rev Endocrinol       Date:  2013-10-01       Impact factor: 43.330

3.  Down-regulation of miR-301a suppresses pro-inflammatory cytokines in Toll-like receptor-triggered macrophages.

Authors:  Lisong Huang; Yin Liu; Liqiu Wang; Ruifeng Chen; Wei Ge; Zhusen Lin; Yun Zhang; Shuyuan Liu; Yi Shan; Qingxian Lin; Minghong Jiang
Journal:  Immunology       Date:  2013-11       Impact factor: 7.397

4.  Transcriptome analysis of epigenetically modulated genome indicates signature genes in manifestation of type 1 diabetes and its prevention in NOD mice.

Authors:  Sundararajan Jayaraman; Akshay Patel; Arathi Jayaraman; Vasu Patel; Mark Holterman; Bellur Prabhakar
Journal:  PLoS One       Date:  2013-01-30       Impact factor: 3.240

5.  HDACi Valproic Acid (VPA) and Suberoylanilide Hydroxamic Acid (SAHA) Delay but Fail to Protect against Warm Hepatic Ischemia-Reperfusion Injury.

Authors:  Dietrich A Ruess; Moriz Probst; Goran Marjanovic; Uwe A Wittel; Ulrich T Hopt; Tobias Keck; Dirk Bausch
Journal:  PLoS One       Date:  2016-08-11       Impact factor: 3.240

  5 in total

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