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Analyzing the Parkinson's Disease Mouse Model Induced by Adeno-associated Viral Vectors Encoding Human α-Synuclein
Published on: July 29, 2022
Common microRNA regulated pathways in Alzheimer's and Parkinson's disease
Betina Awuson-David1, Adrian C Williams2, Benjamin Wright2
1School of Biomedical Sciences, Institute of Clinical Sciences, University of Birmingham, Birmingham, United Kingdom.
Abstract:
MicroRNAs (miRNAs) are small non-coding RNAs involved in gene regulation. Recently, miRNA dysregulation has been found in neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD). The diagnosis of Alzheimer's and Parkinson's is currently challenging, mainly occurring when pathology is already present, and although treatments are available for both diseases, the role of treatment is primarily to prevent or delay the progress of the diseases instead of fully overcoming the diseases. Therefore, the challenge in the near future will be to determine effective drugs to tackle the dysregulated biological pathways in neurodegenerative diseases. In the present study, we describe the dysregulation of miRNAs in blood of Alzheimer's and Parkinson's patients with the aim to identify common mechanisms between the 2 pathologies and potentially to identify common therapeutic targets which can stop or delay the progression of two most frequent neuropathologies. Two independent systematic reviews, bioinformatic analysis, and experiment validation were performed to identify whether AD and PD share common pathways. A total of 15 common miRNAs were found in the literature and 13 common KEGG pathways. Among the common miRNAs, two were selected for validation in a small cohort of AD and PD patients. Let-7f-5p and miR-29b-3p showed to be good predictors in blood of PD patients.
Insights
MicroRNAs (miRNAs) are implicated in Alzheimer's and Parkinson's diseases. This study identified common miRNA pathways and potential blood biomarkers, like let-7f-5p and miR-29b-3p, for Parkinson's disease diagnosis.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression.
- Dysregulation of miRNAs is increasingly linked to neurodegenerative diseases, including Alzheimer's disease (AD) and Parkinson's disease (PD).
- Current diagnostic methods for AD and PD are often late-stage, highlighting the need for early detection and novel therapeutic targets.
Purpose of the Study:
- To identify common molecular mechanisms and potential therapeutic targets shared between Alzheimer's disease and Parkinson's disease by analyzing miRNA dysregulation.
- To explore the utility of blood-based miRNAs as biomarkers for neurodegenerative diseases.
Main Methods:
- Conducted two independent systematic reviews to collate existing literature on miRNA dysregulation in AD and PD.
- Performed bioinformatic analysis to identify common miRNAs and pathways (KEGG) between the two diseases.
- Validated the expression of selected common miRNAs in a small cohort of AD and PD patients.
Main Results:
- Identified 15 common miRNAs and 13 common KEGG pathways implicated in both AD and PD.
- The miRNAs let-7f-5p and miR-29b-3p were found to be significantly dysregulated.
- Let-7f-5p and miR-29b-3p demonstrated potential as predictive biomarkers in the blood of Parkinson's disease patients.
Conclusions:
- Alzheimer's disease and Parkinson's disease share common underlying miRNA-mediated biological pathways.
- Specific miRNAs, such as let-7f-5p and miR-29b-3p, may serve as valuable blood-based biomarkers for Parkinson's disease.
- Further research into these common pathways could lead to the development of novel, shared therapeutic strategies for neurodegenerative diseases.
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