# The Expanding Role of Non-Coding RNAs in Neurodegenerative Diseases: From Biomarkers to Therapeutic Targets

**Authors:** Xuezhi Zhao, Yongquan Zheng, Xiaoyu Cai, Yao Yao, Dongxu Qin

PMC · DOI: 10.3390/ph19010092 · 2026-01-03

## TL;DR

Non-coding RNAs are becoming key players in understanding and treating neurodegenerative diseases like Alzheimer's and Parkinson's.

## Contribution

This review highlights the expanding roles of non-coding RNAs as biomarkers and therapeutic targets in neurodegenerative diseases.

## Key findings

- Non-coding RNAs influence synaptic function, proteostasis, and neuroinflammation in neurodegenerative diseases.
- They show potential as biomarkers for early detection and disease monitoring.
- RNA-targeted therapies, such as antisense oligonucleotides and siRNAs, are being explored for clinical translation.

## Abstract

Non-coding RNAs have emerged as central regulators of gene expression in neurodegenerative diseases, offering new opportunities for diagnosis and therapy. This review synthesizes current knowledge on microRNAs, long non-coding RNAs, and circular RNAs in Alzheimer’s disease, Parkinson’s disease, and amyotrophic lateral sclerosis, emphasizing their roles in synaptic function, proteostasis, mitochondrial biology, and neuroinflammation. We evaluate evidence supporting non-coding RNAs as circulating and tissue-based biomarkers for early detection, disease monitoring, and patient stratification, and we compare analytical platforms and biofluid sources. Mechanistic insights reveal how non-coding RNAs modulate pathogenic protein aggregation, neuronal excitability, immune cell crosstalk, and blood–brain barrier integrity. Translational efforts toward RNA-targeted interventions are reviewed, including antisense oligonucleotides, small interfering RNAs, miRNA mimics and inhibitors, circular RNA decoys, and extracellular vesicle-mediated delivery systems. We discuss pharmacological modulation, delivery challenges, safety concerns, and strategies to enhance specificity and CNS penetration. Finally, we outline emerging computational and multi-omics approaches to prioritize therapeutic targets and propose a roadmap for advancing non-coding RNA research from preclinical models to clinical trials. Addressing biological heterogeneity and delivery barriers will be pivotal to realizing the diagnostic and therapeutic promise of the non-coding transcriptome in neurodegenerative disease. Collaboration across disciplines and rigorous clinical validation are urgently needed.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975), Parkinson’s disease (MONDO:0005180), amyotrophic lateral sclerosis (MONDO:0004976)

## Full-text entities

- **Diseases:** neuroinflammation (MESH:D000090862), Neurodegenerative Diseases (MESH:D019636), Alzheimer's disease (MESH:D000544), Parkinson's disease (MESH:D010300), amyotrophic lateral sclerosis (MESH:D000690)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12844880/full.md

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Source: https://tomesphere.com/paper/PMC12844880