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开启痴呆症的DNA甲基化组研究。

Opening up the DNA methylome of dementia.

作者信息

Delgado-Morales R, Esteller M

机构信息

Cancer Epigenetics and Biology Program, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet del Llobregat, Barcelona, Spain.

Department of Physiological Sciences II, School of Medicine, University of Barcelona, Barcelona, Spain.

出版信息

Mol Psychiatry. 2017 Apr;22(4):485-496. doi: 10.1038/mp.2016.242. Epub 2017 Jan 3.

DOI:10.1038/mp.2016.242
PMID:28044062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5378809/
Abstract

Dementia is a complex clinical condition characterized by several cognitive impairments that interfere with patient independence in executing everyday tasks. Various neurodegenerative disorders have dementia in common among their clinical manifestations. In addition, these diseases, such as Alzheimer's disease, Parkinson's disease, dementia with Lewy bodies and frontotemporal dementia, share molecular alterations at the neuropathological level. In recent years, the field of neuroepigenetics has expanded massively and it is now clear that epigenetic processes, such as DNA methylation, are mechanisms involved in both normal and pathological brain function. Despite the persistent methodological and conceptual caveats, it has been reported that several genes fundamental to the development of neurodegenerative disorders are deregulated by aberrant methylation patterns of their promoters, and even common epigenetic signatures for some dementia-associated pathologies have been identified. Therefore, understanding the epigenetic mechanisms that are altered in dementia, especially those associated with the initial phases, will allow us not only to understand the etiopathology of dementia and its progression but also to design effective therapies to reduce this global public health problem. This review provides an in-depth summary of our current knowledge about DNA methylation in dementia, focusing exclusively on the analyses performed in human brain.

摘要

痴呆症是一种复杂的临床病症,其特征在于多种认知障碍,这些障碍会干扰患者独立完成日常任务的能力。各种神经退行性疾病在临床表现中都有痴呆症这一共同特征。此外,这些疾病,如阿尔茨海默病、帕金森病、路易体痴呆和额颞叶痴呆,在神经病理学水平上存在分子改变。近年来,神经表观遗传学领域得到了极大的扩展,现在很清楚,表观遗传过程,如DNA甲基化,是参与正常和病理脑功能的机制。尽管存在持续的方法学和概念上的限制,但据报道,神经退行性疾病发展的几个关键基因因其启动子的异常甲基化模式而失调,甚至已经确定了一些与痴呆相关病理的常见表观遗传特征。因此,了解痴呆症中发生改变的表观遗传机制,尤其是那些与初始阶段相关的机制,将不仅使我们能够理解痴呆症的病因病理及其进展,还能设计出有效的治疗方法来减少这一全球公共卫生问题。本综述深入总结了我们目前关于痴呆症中DNA甲基化的知识,仅专注于在人类大脑中进行的分析。

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