Juan-Juan Wang, Shao-Wei Ding
The diagnosis of rheumatoid arthritis (RA) remains challenging because of the limitations of existing biomarkers. The purpose of the study was to investigate the potential of miR-488-3p in serum as a biomarker for RA and to reveal its potential mechanism of action. The study included 135 RA patients, 130 osteoarthritis (OA) patients, and 125 healthy controls. miR-488-3p expression levels were examined by RT-qPCR. The mechanism of action was analyzed by functional tests (CCK-8, flow cytometry, ELISA) and target validation experiments (luciferase reporter gene, RIP). Serum miR-488-3p expression levels were significantly lower in RA patients than in osteoarthritis (OA) patients and healthy controls (p < 0.001). ROC curve analysis showed that miR-488-3p had a high diagnostic accuracy in distinguishing RA from healthy controls and OA patients. miR-488-3p negatively correlated with erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP), rheumatoid factor (RF), and DAS28 scores. Functional validation revealed that overexpression of miR-488-3p inhibited the proliferation and inflammatory response of synoviocytes while inducing apoptosis. Mechanistic studies showed that miR-488-3p could directly target Rho-associated coiled-coil containing protein kinase 1 (ROCK1), which mediates its protective effects. Serum miR-488-3p holds promise as a novel non-invasive diagnostic marker for RA and protects synoviocyte from injury.