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揭开帕金森病之谜:微小RNA在调控、诊断及治疗中的作用

Unlocking Parkinson's disease: the role of microRNAs in regulation, diagnosis, and therapy.

作者信息

Li Xiaodong, Fu Qiang, Guo Mei, Du Yang, Cheng Yong

机构信息

Center on Translational Neuroscience, College of Life and Environmental Sciences, Minzu University of China, 27th South Zhongguancun Avenue, Haidian District, Beijing, 100081, China.

Institute of National Security, Minzu University of China, Haidian District, Beijing, 100081, China.

出版信息

Apoptosis. 2025 May 1. doi: 10.1007/s10495-025-02117-w.

Abstract

Parkinson's disease (PD), the second most prevalent neurodegenerative disorder globally, imposes substantial healthcare burdens on aging populations. The pathogenesis of PD is complex and multifaceted. Emerging evidence highlights microRNA (miRNA) dysregulation as a critical regulatory layer that drives PD progression. These small noncoding RNAs mediate posttranscriptional gene regulation through target mRNA binding, inducing either transcript degradation or translational repression. This article reviews the distinct miRNAs that orchestrate PD pathogenesis by disrupting mitochondrial homeostasis, lysosomal clearance pathways, ferroptosis regulation, and neuroinflammatory responses. Notably, some miRNAs achieve these effects by selectively targeting risk genes central to PD pathology. Crucially, certain miRNAs exhibit aberrant expression patterns in the brain tissues and biofluids of PD patients or models, highlighting their potential as minimally invasive diagnostic or prognostic biomarkers. Furthermore, this review highlights the novel role of exosomes as miRNA carriers, offering innovative possibilities for PD therapeutic interventions. With the deepening understanding of miRNA research advances in PD, we propose that these insights may not only inform PD treatment strategies but also hold relevance for addressing other genetic disorders.

摘要

帕金森病(PD)是全球第二常见的神经退行性疾病,给老龄化人口带来了沉重的医疗负担。PD的发病机制复杂且多方面。新出现的证据表明,微小RNA(miRNA)失调是驱动PD进展的关键调控层面。这些小的非编码RNA通过与靶mRNA结合介导转录后基因调控,导致转录本降解或翻译抑制。本文综述了通过破坏线粒体稳态、溶酶体清除途径、铁死亡调节和神经炎症反应来协调PD发病机制的不同miRNA。值得注意的是,一些miRNA通过选择性靶向PD病理学核心的风险基因来实现这些作用。至关重要的是,某些miRNA在PD患者或模型的脑组织和生物流体中表现出异常表达模式,凸显了它们作为微创诊断或预后生物标志物的潜力。此外,本综述强调了外泌体作为miRNA载体的新作用,为PD治疗干预提供了创新可能性。随着对PD中miRNA研究进展的深入理解,我们提出这些见解不仅可能为PD治疗策略提供信息,而且对解决其他遗传疾病也具有相关性。

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