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miR-10 and Its Negative Correlation with Serum IL-35 Concentration and Positive Correlation with STAT5a Expression in
Agnieszka Paradowska-Gorycka1, Anna Wajda1, Ewa Rzeszotarska1
1Department of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637 Warsaw, Poland.
International Journal of Molecular Sciences
|July 27, 2022
Summary
Selected microRNAs (miRNAs) in serum show potential as biomarkers for rheumatoid arthritis (RA). Specific miRNA levels correlate with disease activity and transcription factors, offering insights into RA and osteoarthritis (OA) pathogenesis.
Area of Science:
- Immunology
- Molecular Biology
- Biochemistry
Background:
- Circulating cell-free miRNAs are emerging as non-invasive biomarkers.
- Their epigenetic roles offer insights into disease mechanisms, particularly in oncology.
- Limited research exists on miRNA associations with immune responses in non-oncological diseases like RA.
Purpose of the Study:
- To investigate the association between serum miRNAs and Th17/Treg transcription factors in rheumatoid arthritis (RA).
- To explore potential correlations between specific miRNAs and clinical features in RA and osteoarthritis (OA) patients.
Main Methods:
- Serum miRNA levels were analyzed using LNA miRNA PCR assays in RA, OA, and healthy control (HC) subjects.
- Correlations were examined between miRNA expression, serum cytokine levels, and mRNA expression of key transcription factors (e.g., STAT5a, SMAD3, HIF1, RORc).
Main Results:
- miR-10 was exclusively detected in RA patients, correlating with IL-35 and STAT5a, and trending with disease activity.
- miR-326 was upregulated in RA patients with rheumatoid factor positivity.
- In HC, miR-26 correlated with IL-21 and SMAD3.
- In OA, miR-126 correlated with HIF1, and miR-146 with RORc.
Conclusions:
- Differential associations between serum miRNAs and transcription factor expression suggest their potential roles in RA and OA diagnosis and progression.
- Specific miRNAs like miR-10 and miR-326 may serve as valuable biomarkers for RA.
- These findings highlight the utility of miRNAs in understanding the pathogenesis of inflammatory joint diseases.
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