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靶向 Class IIa HDACs:表型和抑制剂的启示。

Targeting Class IIa HDACs: Insights from Phenotypes and Inhibitors.

机构信息

Division of Chemistry and Structural Biology, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia | Centre for Inflammation and Disease Research, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia | Australian Research Council Centre of Excellence in Advanced Molecular Imaging, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.

Division of Chemistry and Structural Biology, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.

出版信息

Curr Med Chem. 2021;28(42):8628-8672. doi: 10.2174/0929867328666210629160647.

Abstract

This review summarizes key literature defining the phenotypes of individual class IIa HDAC proteins and compounds that selectively target their enzymatic catalytic domain (CD). The focus is on the effects of class IIa HDACs in physiological and pathological conditions, both in vitro and in vivo, and on their mode of action in regulating genes, upstream proteins and signaling pathways. Phenotype studies further demonstrate either beneficial or detrimental effects of silencing selected class IIa HDACs or their enzymatic properties. We also summarize the knowledge gained from structure-activity relationships of CD inhibitors as well as molecular mechanisms underpinning isozyme selectivity where crystal structures or modelling studies are available. Given that the number of genes affected by silencing class IIa HDACs is much smaller than class I, the role of gene regulation of class IIa HDACs could be much more selective. Since class IIa HDACs have restricted tissue distributions and multiple functions independent of their CD, targeting the CD of class IIa HDACs could lead to more selective therapeutic agents with significantly fewer side-effects than other HDAC ligands.

摘要

这篇综述总结了定义个体 IIa 类 HDAC 蛋白表型的关键文献,以及选择性针对其酶催化结构域 (CD) 的化合物。重点介绍了 IIa 类 HDAC 在体外和体内的生理和病理条件下的作用,以及它们在调节基因、上游蛋白和信号通路方面的作用模式。表型研究进一步证明了沉默选定的 IIa 类 HDAC 或其酶特性有益或有害的影响。我们还总结了 CD 抑制剂的构效关系以及分子机制的知识,这些知识是基于晶体结构或建模研究可用的同工酶选择性。鉴于沉默 IIa 类 HDAC 所影响的基因数量远少于 I 类,因此 IIa 类 HDAC 的基因调控作用可能更加具有选择性。由于 IIa 类 HDAC 的组织分布有限,并且具有独立于其 CD 的多种功能,因此靶向 IIa 类 HDAC 的 CD 可能会产生比其他 HDAC 配体更具选择性的治疗药物,副作用也明显更少。

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