A new perspective on Alzheimer's disease: microRNAs and circular RNAs

Shahidee Zainal Abidin1,2, Nurul Asykin Mat Pauzi1, Nur Izzati Mansor3

  • 1Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, Terengganu, Malaysia.

Frontiers in Genetics
|October 4, 2023
PubMed

Insights

MicroRNAs (miRNAs) and circular RNAs (circRNAs) are implicated in Alzheimer's disease (AD) pathogenesis. This review examines altered miRNA expression in AD patients and the emerging role of circRNAs as potential biomarkers and therapeutic targets.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Genetics

Background:

  • MicroRNAs (miRNAs) are key regulators in Alzheimer's disease (AD) pathogenesis, influencing Aβ metabolism, tau phosphorylation, neuroinflammation, and synaptic function.
  • miRNA activity is modulated by factors like subcellular localization, miRNA-mRNA abundance, and binding affinity, with extracellular miRNAs transported via exosomes.
  • Circular RNAs (circRNAs), a novel class of non-coding RNAs, regulate gene expression via interactions with miRNAs, though their precise mechanisms in AD are under investigation.

Purpose of the Study:

  • To comprehensively review alterations in miRNA expression across various sources (blood, exosomes, CSF, brain) in Alzheimer's disease (AD) patients.
  • To explore the emerging role of circular RNAs (circRNAs) in the pathogenesis of AD.
  • To discuss the potential of miRNAs and circRNAs as diagnostic biomarkers and therapeutic targets for AD.

Main Methods:

  • Literature review of studies investigating miRNA expression profiles in Alzheimer's disease.
  • Analysis of research on the involvement of circular RNAs in AD pathology.
  • Synthesis of current understanding of miRNA and circRNA functions and interactions in neurodegenerative diseases.

Main Results:

  • Significant alterations in miRNA expression are observed in peripheral blood, exosomes, cerebrospinal fluid, and brain tissue of AD patients.
  • Emerging evidence suggests circRNAs play a role in AD pathogenesis, potentially through interactions with miRNAs.
  • The complexity of AD pathology presents challenges for miRNA-based diagnostics, necessitating further research.

Conclusions:

  • miRNAs are critical players in AD, with altered expression patterns offering diagnostic potential across different biological fluids and tissues.
  • circRNAs represent a promising area of research for understanding AD mechanisms and developing novel therapeutic strategies.
  • Further investigation into miRNA and circRNA profiles is essential for advancing AD diagnostics and therapeutics.

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