Chang Ting-Kuo, Ho Trung-Loc, Lin Yen-You, Thuong Le Huynh Hoai, Lai Kuan-Ying, Tsai Chun-Hao, Liaw Chih-Chuang, Tang Chih-Hsin
Department of Medicine, Mackay Medical College, New Taipei, Taiwan.
Division of Spine Surgery, Department of Orthopedic Surgery, MacKay Memorial Hospital, New Taipei, Taiwan.
Int J Biol Sci. 2025 Jan 21;21(4):1378-1390. doi: 10.7150/ijbs.108789. eCollection 2025.
Arthritis is a chronic inflammatory disease that causes joint damage, with osteoarthritis (OA) and rheumatoid arthritis (RA) being the most common types. Both conditions are characterized by cartilage degradation due to an imbalance between repair and breakdown processes. Chondrocytes, the key cells in articular cartilage, maintain its structure by producing an extracellular matrix rich in aggrecan and type II collagen (COL2). MicroRNAs (miRNAs), small noncoding RNAs, regulate genes critical for cartilage balance and are involved in the progression and treatment of OA and RA. Recently, herbal medicines have gained attention for arthritis treatment. Ugonin P, a flavonoid from , is known for its antioxidant and anticancer effects, but its role in cartilage homeostasis is unclear. This study explores ugonin P's chondrogenic effects and its molecular mechanisms involving miRNA regulation. Analysis of Gene Expression Omnibus (GEO) data and clinical samples revealed reduced aggrecan and COL2 levels in OA and RA, while miR-3074-5p levels were elevated, suppressing these proteins. Ugonin P, without affecting cell viability, enhanced aggrecan and COL2 production and promoted chondrocyte differentiation by downregulating miR-3074-5p and activating MAPK pathways. These findings suggest ugonin P as a promising therapeutic candidate for arthritis management.
关节炎是一种导致关节损伤的慢性炎症性疾病,骨关节炎(OA)和类风湿关节炎(RA)是最常见的类型。这两种病症的特征都是由于修复和分解过程之间的失衡导致软骨降解。软骨细胞是关节软骨中的关键细胞,通过产生富含聚集蛋白聚糖和II型胶原蛋白(COL2)的细胞外基质来维持其结构。微小RNA(miRNA)是小的非编码RNA,可调节对软骨平衡至关重要的基因,并参与OA和RA的进展及治疗。最近,草药在关节炎治疗中受到关注。乌冈宁P是一种来自[具体来源未提及]的黄酮类化合物,以其抗氧化和抗癌作用而闻名,但其在软骨稳态中的作用尚不清楚。本研究探讨了乌冈宁P的软骨生成作用及其涉及miRNA调节的分子机制。对基因表达综合数据库(GEO)数据和临床样本的分析显示,OA和RA中聚集蛋白聚糖和COL2水平降低,而miR-3074-5p水平升高,抑制了这些蛋白质。乌冈宁P在不影响细胞活力的情况下,通过下调miR-3074-5p并激活丝裂原活化蛋白激酶(MAPK)途径,增强了聚集蛋白聚糖和COL2的产生,并促进了软骨细胞分化。这些发现表明乌冈宁P是一种有前途的关节炎治疗候选药物。