Cited by 52MicroRNA in disease regulationTreatment of Major DepressionRNA Interference and Gene Delivery

Thinking small: towards microRNA-based therapeutics for anxiety disorders

Scott, Karen A, Hoban, Alan E, Clarke, Gerard, Moloney, Gerard M, Dinan, Timothy G, Cryan, John F·2015·Expert Opinion on Investigational Drugs

Abstract

Introduction Anxiety disorders are the most frequently diagnosed psychiatric conditions, negatively affecting quality of life and creating a significant economic burden. These complex disorders are extremely difficult to treat, and there is a great need for novel therapeutics with greater efficacy and minimal adverse side effects. Areas covered In this review, the authors describe the role that microribonucleic acids (microRNA or miRNA) play in the development of anxiety disorders and their potential to serve as biomarkers of disease as well as targets for pharmacological treatment. Furthermore, the authors discuss the current state of miRNA research, including both preclinical and clinical studies of anxiety disorders. Expert opinion There is mounting evidence that circulating miRNA may serve as biomarkers of disease and play a role in the development of disease, including psychiatric conditions such as anxiety disorders. Great strides have been made in cancer research, with miRNA-based therapies already in use in clinical studies. However, the use of miRNA for the treatment of neurological disorders, and psychiatric disorders in particular, is still in its nascent stage. The development of safe compounds that are able to cross the blood-brain barrier and target specific cell populations, which are relevant to anxiety-related neurocircuitry, is paramount for the emergence of novel, efficacious miRNA-based therapies in clinical settings.

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Crossref · 10.1517/13543784.2014.997873

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  • miRNAs regulate gene expression through translational repression and inhibition, and they are viable targets for intervention in neuropsychiatric disease.

    “miRNAs regulate gene expression through translational repression and inhibition, and they are viable targets for intervention in neuropsychiatric disease (Issler and Chen, 2015;O'Connor et al., 2013;Scott et al., 2015).”

    From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Scott et al., 2015

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References 114 · Cited by 52

Authors
Scott, K. A., Hoban, A. E., Clarke, G., Moloney, G. M., Dinan, T. G., & Cryan, J. F.
Affiliations
University College Cork (IE)
Venue
Expert Opinion on Investigational Drugs
Published
2015-01-08
Volume
24
Issue
4
Pages
529-542
ISSN
  • 1354-3784 (ISSN-L)
  • 1744-7658
OpenAlex
W1987131356
Cited by
52
References
114
Citations by year
2026: 4 · 2025: 5 · 2024: 6 · 2023: 5 · 2022: 3 · 2021: 5 · 2020: 5 · 2019: 5 · 2018: 1 · 2017: 5 · 2016: 5 · 2015: 3
FWCI
0.45
Type
journal article
Language
en
Open access
closed
Locations
  • Expert Opinion on Investigational Drugs (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
Keywords
microRNA, anxiety disorders, miRNA-based therapy, circulating microRNA biomarkers, mental illness, blood-brain barrier, neurocircuitry, neurological disorders
MeSH terms
Animals, Anxiety Disorders, Blood-Brain Barrier, Humans, Quality of Life, Anti-Anxiety Agents, Cost of Illness, MicroRNAs, Molecular Targeted Therapy

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