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探索表观遗传药物发现领域。

Exploring the epigenetic drug discovery landscape.

作者信息

Prachayasittikul Veda, Prathipati Philip, Pratiwi Reny, Phanus-Umporn Chuleeporn, Malik Aijaz Ahmad, Schaduangrat Nalini, Seenprachawong Kanokwan, Wongchitrat Prapimpun, Supokawej Aungkura, Prachayasittikul Virapong, Wikberg Jarl E S, Nantasenamat Chanin

机构信息

a Center of Data Mining and Biomedical Informatics, Faculty of Medical Technology , Mahidol University , Bangkok , Thailand.

b National Institutes of Biomedical Innovation, Health and Nutrition , Osaka , Japan.

出版信息

Expert Opin Drug Discov. 2017 Apr;12(4):345-362. doi: 10.1080/17460441.2017.1295954. Epub 2017 Feb 28.

Abstract

Epigenetic modification has been implicated in a wide range of diseases and the ability to modulate such systems is a lucrative therapeutic strategy in drug discovery. Areas covered: This article focuses on the concepts and drug discovery aspects of epigenomics. This is achieved by providing a survey of the following concepts: (i) factors influencing epigenetics, (ii) diseases arising from epigenetics, (iii) epigenetic enzymes as druggable targets along with coverage of existing FDA-approved drugs and pharmacological agents, and (iv) drug repurposing/repositioning as a means for rapid discovery of pharmacological agents targeting epigenetics. Expert opinion: Despite significant interests in targeting epigenetic modifiers as a therapeutic route, certain classes of target proteins are heavily studied while some are less characterized. Thus, such orphan target proteins are not yet druggable with limited report of active modulators. Current research points towards a great future with novel drugs directed to the many complex multifactorial diseases of humans, which are still often poorly understood and difficult to treat.

摘要

表观遗传修饰与多种疾病有关,调节此类系统的能力是药物发现中一种有利可图的治疗策略。涵盖领域:本文重点关注表观基因组学的概念和药物发现方面。这是通过对以下概念进行综述来实现的:(i)影响表观遗传学的因素,(ii)由表观遗传学引起的疾病,(iii)作为可成药靶点的表观遗传酶以及现有FDA批准的药物和药理剂的介绍,以及(iv)药物重新利用/重新定位作为快速发现靶向表观遗传学的药理剂的一种手段。专家观点:尽管将表观遗传修饰剂作为治疗途径有很大兴趣,但某些类别的靶蛋白被大量研究,而有些则特征较少。因此,此类孤儿靶蛋白目前还难以成药,针对它们的活性调节剂的报道有限。当前的研究表明,未来有望开发出针对人类许多复杂的多因素疾病的新型药物,这些疾病目前往往仍了解不足且难以治疗。

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