Relationship of epigenetic variability of miR-124 to extracellular matrix remodelling and age-related MMP-3 expression in rheumatoid arthritis
Language English Country Slovakia Media print-electronic
Document type Journal Article
PubMed
30431436
DOI
10.4149/gpb_2018024
Knihovny.cz E-resources
- MeSH
- Peptides, Cyclic MeSH
- Extracellular Matrix MeSH
- Humans MeSH
- Matrix Metalloproteinase 3 metabolism MeSH
- MicroRNAs genetics MeSH
- Arthritis, Rheumatoid * genetics metabolism MeSH
- Tumor Necrosis Factor-alpha MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Peptides, Cyclic MeSH
- Matrix Metalloproteinase 3 MeSH
- MicroRNAs MeSH
- MIRN124 microRNA, human MeSH Browser
- MMP3 protein, human MeSH Browser
- Tumor Necrosis Factor-alpha MeSH
The aim of study was to examine relation among miR-124 and serum levels of selected cytokines and chemokines, MMP-3, production of auto-antibodies, and factors describing clinical activity (DAS28) and radiographic progression in rheumatoid arthritis (RA). A total of 80 RA patients according to the ACR classification criteria, and 32 control subjects were recruited into study. The measurements of miR-124 and U-6 expression, CRP, anti-CCP, rheumatoid factors (RFs), radiographs of both hands with calculation of total sharp score (TSS), DAS28 and cytokines, chemokines and MMP levels in serum were obtained from all RA patients. miR-124 was down-regulated in RA patients compared to controls (7-fold decrease). The miR-124 expression correlated to MMP-3 levels (p < 0.001), which were in multivariate analysis associated to age of RA onset. Higher levels were detected in younger subjects. No relation of miR-124 expression to measures of RA activity (DAS28 score; TSS), auto-antibodies (anti-CCP, RF, RF IgG, RF IgA, RF IgM), acute inflammatory markers (CRP, IL-6), and other cytokine and chemokines (IL-13, IL-15, IL-8, TNF-α, MCP-1, RANTES) was observed. In conclusion, we present a down-regulation of miR-124 in RA patients and its correlation to MMP-3 levels, which associated to age of RA onset.
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