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Published on: June 13, 2016
MicroRNA Expression Profiling in Psoriatic Arthritis
Andrea Pelosi1, Claudio Lunardi2, Piera Filomena Fiore1
1Immunology Area, Pediatric Hospital Bambino Gesù, Viale San Paolo 15, 00146 Rome, Italy.
Background:
Psoriatic arthritis (PsA) is an inflammatory arthritis, characterized by bone erosions and new bone formation. MicroRNAs (miRNAs) are key regulators of the immune responses. Differential expression of miRNAs has been reported in several inflammatory autoimmune diseases; however, their role in PsA is not fully elucidated. We aimed to identify miRNA expression signatures associated with PsA and to investigate their potential implication in the disease pathogenesis.
Methods:
miRNA microarray was performed in blood cells of PsA patients and healthy controls. miRNA pathway analyses were performed and the global miRNA profiling was combined with transcriptome data in PsA. Deregulation of selected miRNAs was validated by real-time PCR.
Results:
We identified specific miRNA signatures associated with PsA patients with active disease. These miRNAs target pathways relevant in PsA, such as TNF, MAPK, and WNT signaling cascades. Network analysis revealed several miRNAs regulating highly connected genes within the PsA transcriptome. miR-126-3p was the most downregulated miRNA in active patients. Noteworthy, miR-126 overexpression induced a decreased expression of genes implicated in PsA.
Conclusions:
This study sheds light on some epigenetic aspects of PsA identifying specific miRNAs, which may represent promising candidates as biomarkers and/or for the design of novel therapeutic strategies in PsA.
Insights
Researchers identified specific microRNA (miRNA) signatures in psoriatic arthritis (PsA) patients. Downregulated miR-126-3p in active PsA suggests potential as a biomarker and therapeutic target.
Area of Science:
- Immunology
- Genetics
- Molecular Biology
Background:
- Psoriatic arthritis (PsA) is an inflammatory condition involving bone erosion and formation.
- MicroRNAs (miRNAs) are crucial immune response regulators, but their role in PsA pathogenesis is unclear.
Purpose of the Study:
- To identify miRNA expression signatures linked to PsA.
- To explore the potential involvement of these miRNAs in PsA pathogenesis.
Main Methods:
- MicroRNA microarray analysis in blood cells from PsA patients and healthy controls.
- Pathway and transcriptome analyses integrating global miRNA profiling with gene expression data.
- Validation of selected miRNA deregulation using real-time PCR.
Main Results:
- Identified distinct miRNA signatures in PsA patients with active disease.
- Targeted pathways include TNF, MAPK, and WNT signaling.
- miR-126-3p was significantly downregulated in active PsA; its overexpression reduced PsA-implicated gene expression.
Conclusions:
- This study highlights epigenetic factors in PsA by identifying specific miRNAs.
- These miRNAs show promise as potential biomarkers for PsA.
- Identified miRNAs may guide the development of novel therapeutic strategies for PsA.
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