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针对阿尔茨海默病的自噬靶向治疗距离临床应用还有多远?临床研究中自噬调节剂综述。

How close is autophagy-targeting therapy for Alzheimer's disease to clinical use? A summary of autophagy modulators in clinical studies.

作者信息

Fernandes Sofia Miranda, Mayer Johanna, Nilsson Per, Shimozawa Makoto

机构信息

Department of Neurobiology, Care Sciences and Society, Division of Neurogeriatrics, Center for Alzheimer Research, Karolinska Institutet, Stockholm, Sweden.

出版信息

Front Cell Dev Biol. 2025 Jan 8;12:1520949. doi: 10.3389/fcell.2024.1520949. eCollection 2024.

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder clinically characterized by progressive decline of memory and cognitive functions, and it is the leading cause of dementia accounting for 60%-80% of dementia patients. A pathological hallmark of AD is the accumulation of aberrant protein/peptide aggregates such as extracellular amyloid plaques containing amyloid-beta peptides and intracellular neurofibrillary tangles composed of hyperphosphorylated tau. These aggregates result from the failure of the proteostasis network, which encompasses protein synthesis, folding, and degradation processes. Autophagy is an intracellular self-digesting system responsible for the degradation of protein aggregates and damaged organelles. Impaired autophagy is observed in most neurodegenerative disorders, indicating the link between autophagy dysfunction and these diseases. A massive accumulation of autophagic vacuoles in neurons in Alzheimer's brains evidences autophagy impairment in AD. Modulating autophagy has been proposed as a therapeutic strategy for AD because of its potential to clear aggregated proteins. However, autophagy modulation therapy for AD is not yet clinically available. This mini-review aims to summarize clinical studies testing potential autophagy modulators for AD and to evaluate their proximity to clinical use. We accessed clinicaltrials.gov provided by the United States National Institutes of Health to identify completed and ongoing clinical trials. Additionally, we discuss the limitations and challenges of these therapies.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,临床上以记忆和认知功能的进行性衰退为特征,它是痴呆症的主要病因,占痴呆症患者的60%-80%。AD的一个病理标志是异常蛋白质/肽聚集体的积累,如含有β-淀粉样肽的细胞外淀粉样斑块和由过度磷酸化的tau组成的细胞内神经原纤维缠结。这些聚集体是由蛋白质稳态网络的故障导致的,该网络包括蛋白质合成、折叠和降解过程。自噬是一种细胞内自我消化系统,负责蛋白质聚集体和受损细胞器的降解。在大多数神经退行性疾病中都观察到自噬受损,这表明自噬功能障碍与这些疾病之间存在联系。阿尔茨海默病患者大脑中神经元内大量自噬泡的积累证明了AD中的自噬损伤。由于自噬具有清除聚集蛋白的潜力,因此调节自噬已被提议作为AD的一种治疗策略。然而,用于AD的自噬调节疗法尚未在临床上应用。这篇小型综述旨在总结测试AD潜在自噬调节剂的临床研究,并评估它们与临床应用的接近程度。我们访问了美国国立卫生研究院提供的clinicaltrials.gov网站,以确定已完成和正在进行的临床试验。此外,我们还讨论了这些疗法的局限性和挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e7/11750832/eff8d892e1d2/fcell-12-1520949-g001.jpg

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