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MiRNA-Mediated Regulation in Osteoarthritis Across Joint Tissues, Including Translational Perspectives in Dogs.
Gabriella Guelfi1, Camilla Capaccia1, Vicente Francisco Ratto1
1Department of Veterinary Medicine, University of Perugia, 06126 Perugia, Italy.
Animals : an Open Access Journal From MDPI
|March 28, 2026
Summary
MicroRNAs (miRNAs) are key regulators in osteoarthritis (OA). This review synthesizes human OA research to guide canine OA studies, identifying circulating miRNAs (cmiRNAs) as promising non-invasive diagnostic targets.
Area of Science:
- Molecular Biology
- Biochemistry
- Veterinary Medicine
Background:
- Osteoarthritis (OA) is a complex, whole-joint disease involving interconnected pathological processes.
- MicroRNAs (miRNAs) are crucial post-transcriptional regulators integrating various disease cues in OA.
- Human OA research extensively links miRNA dysregulation to disease mechanisms and identifies circulating miRNAs (cmiRNAs) as potential biomarkers.
Purpose of the Study:
- To critically synthesize miRNA-mediated regulatory mechanisms in human OA.
- To leverage human OA insights to define research priorities for canine OA.
- To establish a comparative framework for identifying translational targets in canine OA.
Main Methods:
- Literature review synthesizing existing research on miRNAs in human OA.
- Comparative analysis of molecular contexts between human and canine OA.
- Identification of research gaps and priorities in canine miRNA research.
Main Results:
- miRNA dysregulation is implicated in cartilage breakdown, stress response, and inter-tissue communication in human OA.
- Canine OA research on miRNAs is limited, with only one pilot study existing.
- Shared molecular pathways suggest potential for comparative miRNA research.
Conclusions:
- Circulating miRNAs (cmiRNAs) represent promising non-invasive translational targets for canine OA.
- Further experimental validation is needed in canine OA models.
- A comparative framework focusing on shared molecular contexts is essential for advancing canine OA miRNA research.
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