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组蛋白去乙酰化酶抑制剂:对神经退行性疾病的潜在影响

Histone deacetylase inhibitors: possible implications for neurodegenerative disorders.

作者信息

Hahnen Eric, Hauke Jan, Tränkle Christian, Eyüpoglu Ilker Y, Wirth Brunhilde, Blümcke Ingmar

机构信息

Institute of Human Genetics, Institute of Genetics, University of Cologne, 50931 Cologne, Germany.

出版信息

Expert Opin Investig Drugs. 2008 Feb;17(2):169-84. doi: 10.1517/13543784.17.2.169.

Abstract

During the past six years numerous studies identified histone deacetylase (HDAC) inhibitors as candidate drugs for the treatment of neurodegenerative disorders. Two major neuroprotective mechanisms of HDAC inhibitors have been identified, namely the transcriptional activation of disease-modifying genes and the correction of perturbations in histone acetylation homeostasis, which have been shown to be intimately involved in the neurodegenerative pathomechanisms of Huntington's, Parkinson's and Kennedy disease, amyotropic lateral sclerosis, Rubinstein-Taybi syndrome as well as stroke. Based on the promising in vitro and in vivo analyses, clinical trials have been initiated to evaluate the safety and efficacy of HDAC inhibitors for the treatment of devastating diseases such as Huntington's disease, amyotropic lateral sclerosis and spinal muscular atrophy. Here, the authors summarize and discuss the findings on the emerging field of epigenetic therapy strategies in neurodegenerative disorders.

摘要

在过去六年中,大量研究将组蛋白去乙酰化酶(HDAC)抑制剂确定为治疗神经退行性疾病的候选药物。HDAC抑制剂的两种主要神经保护机制已被确定,即疾病修饰基因的转录激活和组蛋白乙酰化稳态紊乱的纠正,这些机制已被证明与亨廷顿舞蹈症、帕金森病、肯尼迪病、肌萎缩侧索硬化症、鲁宾斯坦-泰比综合征以及中风的神经退行性发病机制密切相关。基于体外和体内分析的良好结果,已启动临床试验以评估HDAC抑制剂治疗诸如亨廷顿舞蹈症、肌萎缩侧索硬化症和脊髓性肌萎缩症等毁灭性疾病的安全性和有效性。在此,作者总结并讨论了神经退行性疾病中表观遗传治疗策略这一新兴领域的研究结果。

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