miR-655-3p is a highly accurate diagnostic biomarker for primary osteoarthritis and alleviates joint inflammation by targeting TLR4.

IF 1
Ruye Li, Chao Chen, Deming Chen
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Abstract

Objective: This study aimed to evaluate the potential of miR-655-3p as a diagnostic biomarker for primary osteoarthritis (OA) and to investigate its intrinsic molecular mechanisms as a means of addressing the lack of sensitive early diagnostic biomarkers and targeted anti-inflammatory therapies for this prevalent degenerative joint disorder.

Methods: Quantitative real-time polymerase chain reaction was performed to measure (1) miR-655-3p levels in the serum of 93 primary OA patients and 60 non-OA controls, (2) miR-655-3p levels in the synovial fluid of OA patients, and (3) messenger RNA (mRNA) expression of TLR4, RelA, TNF-α, and IL-6 in the IL-1β-induced OA chondrocyte model. Enzyme-linked immunosorbent assay measured the secretion of IL-6 and TNF-α. Receiver operating characteristic curve (ROC) analysis assessed its diagnostic value in multiple clinical scenarios. Cell function assays investigated cell viability and apoptosis. Target genes were predicted via 3 databases, and the interaction between miR-655-3p and TLR4 was verified by dual-luciferase reporter assay and Western blot. Rescue experiments were performed to confirm the mechanistic specificity.

Results: miR-655-3p was downregulated by 44.8% in OA serum (P < .001) and 46.7% in IL-1β-induced chondrocytes (P < .001). ROC curve analysis showed an overall area under the curve (AUC) of 0.9518 (95% CI: 0.920-0.983), with consistent high accuracy in distinguishing OA from healthy controls (AUC = 0.9509), meniscus injury patients (AUC = 0.9425), and mild OA from controls (AUC = 0.9306). Serum miR- 655-3p levels were negatively correlated with OA severity (American Academy of Orthopaedic Surgeons score, P = .010) and inflammatory factor levels (TNF-α, IL-6, both P < .001). Dual-luciferase assay confirmed TLR4 as a direct target of miR-655-3p; miR 655-3p overexpression reduced TLR4 protein expression by 48.7%, while inhibition increased it by 52.8%. TLR4 overexpression completely reversed the antiinflammatory and anti-apoptotic effects of miR-655-3p in OA chondrocytes.

Conclusion: miR-655-3p is a highly accurate diagnostic biomarker for primary OA, and upregulating miR-655-3p may provide a novel clinical treatment direction by targeting TLR4 to alleviate joint inflammation.   Cite this article as: Li R, Chen C, Chen D. MiR-655-3p is a highly accurate diagnostic biomarker for primary osteoarthritis and alleviates joint inflammation by targeting TLR4. Acta Orthop Traumatol Turc., 2026; 60(4), 0803, doi: 10.5152/j.aott.2026.25803.

miR-655-3p是一种高度准确的原发性骨关节炎诊断生物标志物,并通过靶向TLR4缓解关节炎症。
目的:本研究旨在评估miR-655-3p作为原发性骨关节炎(OA)诊断生物标志物的潜力,并研究其内在分子机制,以解决这种普遍存在的退行性关节疾病缺乏敏感的早期诊断生物标志物和靶向抗炎治疗的问题。方法:采用实时定量聚合酶链反应测定(1)93例原发性OA患者和60例非OA对照组血清中miR-655-3p水平,(2)OA患者滑液中miR-655-3p水平,(3)il -1β诱导OA软骨细胞模型中TLR4、RelA、TNF-α、IL-6 mRNA表达。酶联免疫吸附法测定IL-6和TNF-α的分泌。受试者工作特征曲线(ROC)分析评估其在多种临床情况下的诊断价值。细胞功能测定研究细胞活力和凋亡。通过3个数据库预测靶基因,并通过双荧光素酶报告基因实验和Western blot验证miR-655-3p与TLR4之间的相互作用。进行了救援实验以确认机制特异性。结果:miR-655-3p在OA血清中下调44.8% (P < 0.001),在il -1β诱导的软骨细胞中下调46.7% (P < 0.001)。ROC曲线分析显示,总体曲线下面积(AUC)为0.9518 (95% CI: 0.920 ~ 0.983),在区分OA与健康对照组(AUC = 0.9509)、半月板损伤患者(AUC = 0.9425)和轻度OA与对照组(AUC = 0.9306)方面具有一致的高准确度。血清miR- 655-3p水平与骨性关节炎严重程度(美国骨科学会评分,P = 0.010)及炎症因子(TNF-α、IL-6, P均< 0.001)呈负相关。双荧光素酶检测证实TLR4是miR-655-3p的直接靶点;miR 655-3p过表达使TLR4蛋白表达减少48.7%,抑制使TLR4蛋白表达增加52.8%。TLR4过表达完全逆转了miR-655-3p在OA软骨细胞中的抗炎和抗凋亡作用。结论:miR-655-3p是原发性OA的高精度诊断生物标志物,上调miR-655-3p可能通过靶向TLR4缓解关节炎症,为临床提供新的治疗方向。MiR-655-3p是一种高度准确的原发性骨关节炎诊断生物标志物,并通过靶向TLR4缓解关节炎症。骨科创伤学报。, 2026;[j] .中国科学:地球科学,2016,33 (4),0803,doi: 10.5152/j.aott.2026.25803.]
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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