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Published on: February 6, 2020
Expression of lncRNA NEAT1, miR-21, and IL17 in Rheumatoid Arthritis Patients
Maysa M Haroon1, Gehan A Hegazy2,3, Mohammed A Hassanien4
1Rheumatology Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Researchers found that long noncoding RNA nuclear paraspeckle assembly transcript 1 (NEAT1) and interleukin 17 (IL17) were elevated in rheumatoid arthritis (RA) patients, while micro-RNA 21 (miR-21) was decreased. NEAT1 levels correlated with RA disease activity, suggesting potential as biomarkers.
Area of Science:
- Immunology
- Molecular Biology
- Genetics
Background:
- Rheumatoid arthritis (RA) is a prevalent autoimmune disease with significant patient and societal costs, emphasizing the need for early diagnostic biomarkers.
- Long noncoding RNA nuclear paraspeckle assembly transcript 1 (NEAT1), micro-RNA 21 (miR-21), and interleukin 17 (IL17) are implicated in inflammatory conditions.
Purpose of the Study:
- To investigate the roles of NEAT1, miR-21, and IL17 in rheumatoid arthritis (RA) pathogenesis and activity.
- To assess the potential of NEAT1, miR-21, and IL17 as diagnostic biomarkers or therapeutic targets for RA.
Main Methods:
- Serum expression levels of NEAT1, miR-21, and IL17 were compared between 100 RA patients and 100 healthy controls.
- Correlations between the expression levels of these molecules and RA clinical manifestations, including disease activity scores (DAS-28) and disease duration, were analyzed.
Main Results:
- NEAT1 and IL17 expression levels were significantly upregulated in RA patients compared to controls.
- miR-21 expression was significantly downregulated in RA patients.
- NEAT1 showed a significant positive correlation with joint swelling and tenderness counts and the DAS-28 score. miR-21 negatively correlated with RA disease duration.
Conclusions:
- NEAT1, miR-21, and IL17 exhibit distinct expression patterns in RA patients, with NEAT1 and IL17 upregulated and miR-21 downregulated.
- NEAT1 expression is significantly associated with RA disease activity, indicating its potential as a biomarker.
- Further research is warranted to validate NEAT1, miR-21, and IL17 as reliable biomarkers for RA diagnosis and management.
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