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Long Non-Coding RNAs: Crucial Regulators in Alzheimer's Disease Pathogenesis and Prospects for Precision Medicine.

作者信息

Yang Chenbo, Li Yiwei, Chen Chao, Sun Zexin, Liu Enjie, Wei Na, Liu Xiaonan, Shu Jiao, Zhao Na, Sun Miaomiao

机构信息

Department of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.

Henan Key Laboratory of Tumor Pathology, Zhengzhou University, Zhengzhou, People's Republic of China.

出版信息

Mol Neurobiol. 2025 Jun;62(6):7525-7541. doi: 10.1007/s12035-025-04729-4. Epub 2025 Feb 5.


DOI:10.1007/s12035-025-04729-4
PMID:39907902
Abstract

Long non-coding RNAs (LncRNAs) have emerged as pivotal regulators in the pathogenesis of Alzheimer's disease (AD), a progressive neurodegenerative disorder characterized by cognitive decline and memory loss. With the capacity to modulate gene expression at various levels, LncRNAs are implicated in multiple pathological mechanisms of AD, including amyloid-beta (Aβ) accumulation, tau protein phosphorylation, neuroinflammation, and neuronal apoptosis. Recent studies have highlighted the potential of LncRNAs as diagnostic biomarkers and therapeutic targets due to their differential expression patterns in AD patients. This review synthesizes current knowledge on the role of LncRNAs in AD, focusing on their involvement in key molecular pathways and their promise as indicators for early diagnosis and prognosis. We discuss the regulatory networks of LncRNAs in the context of AD, their interaction with miRNAs, and the implications for developing novel therapeutic strategies. Despite the complexity and variability in LncRNA function, the prospect of harnessing these molecules for precision medicine in AD is gaining momentum. The translational potential of LncRNA-based interventions offers a new frontier in the quest for effective treatments and a deeper understanding of the molecular underpinnings of AD.

摘要

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[1]
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引用本文的文献

[1]
Lead Induces Mitochondrial Dysregulation in SH-SY5Y Neuroblastoma Cells via a lncRNA/circRNA-miRNA-mRNA Interdependent Networks.

Int J Mol Sci. 2025-7-17

[2]
Cannabinerol Restores mRNA Splicing Defects Induced by β-Amyloid in an In Vitro Model of Alzheimer's Disease: A Transcriptomic Study.

Int J Mol Sci. 2025-3-28

本文引用的文献

[1]
Tanshinone IIA improves Alzheimer's disease RNA nuclear-enriched abundant transcript 1/microRNA-291a-3p/member RAS oncogene family Rab22a axis.

World J Psychiatry. 2024-4-19

[2]
Diagnostic value and cognitive regulatory roles of long non-coding RNA UCA1 in Alzheimer's disease.

Neurosci Lett. 2024-4-23

[3]
LINC00472 Regulates Ferroptosis of Neurons in Alzheimer's Disease via FOXO1.

Dement Geriatr Cogn Disord. 2024

[4]
Mechanisms underlying LncRNA SNHG1 regulation of Alzheimer's disease involve DNA methylation.

J Toxicol Environ Health A. 2024-5-18

[5]
Inhibitory effects of β-asarone on lncRNA BACE1-mediated induction of autophagy in a model of Alzheimer's disease.

Behav Brain Res. 2024-4-12

[6]
Combining Multifunctional Delivery System with Blood-Brain Barrier Reversible Opening Strategy for the Enhanced Treatment of Alzheimer's Disease.

Adv Healthc Mater. 2024-3

[7]
LncRNA ENST00000440246.1 Promotes Alzheimer's Disease Progression by Targeting PP2A.

Biochem Genet. 2024-6

[8]
MEG3 activates necroptosis in human neuron xenografts modeling Alzheimer's disease.

Science. 2023-9-15

[9]
Dexmedetomidine Promoted HSPB8 Expression via Inhibiting the lncRNA SNHG14/UPF1 Axis to Inhibit Apoptosis of Nerve Cells in AD : The Role of Dexmedetomidine in AD.

Neurotox Res. 2023-10

[10]
Triptolide improves Alzheimer's disease by regulating the NF‑κB signaling pathway through the lncRNA NEAT1/microRNA 361‑3p/TRAF2 axis.

Exp Ther Med. 2023-8-1

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