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Expression of the deubiquitinase cylindromatosis in articular cartilage and subchondral bone is associated with the severity of knee osteoarthritis

机译:去泛素化酶圆柱化病在关节软骨和软骨下骨中的表达与膝骨关节炎的严重程度有关

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摘要

Cylindromatosis (CYLD) is a deubiquitinating enzyme that regulates multiple key signaling pathways involved in the pathophysiology of knee osteoarthritis (KOA). Previous studies have indicated that the expression of CYLD in the articular cartilage of patients with KOA is significantly higher than in healthy controls. However, limited data are available regarding the association between CYLD expression and the severity of KOA. The aim of the present study was to investigate the association between CYLD expression in joint tissues and the severity of KOA. A total of 156 individual tibial plateau samples were obtained between January 2011 and January 2016 from patients that had undergone total knee arthroplasty due to KOA or from healthy controls. The severity of KOA was evaluated using the Kellgren Lawrence (KL) and Mankin scoring systems. Additionally, CYLD expression in the articular cartilage and subchondral bone was analyzed using immunohistochemistry. Compared with the healthy controls, patients with KOA exhibited significantly increased CYLD levels in the articular cartilage (6.53±2.01 vs. 28.69±13.23, P<0.001) and significantly decreased CYLD levels in the subchondral bone (11.46±2.34 vs. 3.50±2.54, P<0.001). Correlation analysis indicated that CYLD expression in the articular cartilage was positively correlated with the KL (r=0.837, P<0.001) and Mankin scores (r=0.925, P<0.001), while its expression in the subchondral bone was negatively correlated with the KL (r=−0.802, P<0.001) and Mankin scores (r=−0.844, P<0.001). The results of the present study demonstrate that CYLD levels in the articular cartilage and subchondral bone are associated with the severity of KOA. Thus, CYLD may be a potential diagnostic and predictive biomarker for KOA and a novel target in its treatment.
机译:圆柱状增生症(CYLD)是一种去泛素化酶,可调节涉及膝骨关节炎(KOA)病理生理的多个关键信号通路。先前的研究表明,CYA在KOA患者关节软骨中的表达明显高于健康对照者。但是,关于CYLD表达与KOA严重性之间的关联的可用数据有限。本研究的目的是研究关节组织中CYLD表达与KOA严重程度之间的关系。在2011年1月至2016年1月之间,从因KOA进行了全膝关节置换术的患者或健康对照中获得了总共156个胫骨平台样本。使用Kellgren Lawrence(KL)和Mankin评分系统评估了KOA的严重程度。另外,使用免疫组织化学分析了CY软骨在关节软骨和软骨下骨中的表达。与健康对照组相比,KOA患者的关节软骨CYLD水平显着升高(6.53±2.01比28.69±13.23,P <0.001),软骨下骨CYLD水平显着降低(11.46±2.34 vs.3.50±2.54)。 ,P <0.001)。相关分析表明,CYLD在关节软骨中的表达与KL(r = 0.837,P <0.001)和Mankin评分(r = 0.925,P <0.001)呈正相关,而在软骨下骨中的表达与软骨的负相关。 KL(r = -0.802,P <0.001)和Mankin得分(r = -0.844,P <0.001)。本研究的结果表明,关节软骨和软骨下骨中的CYLD水平与KOA的严重程度有关。因此,CYLD可能是KOA的潜在诊断和预测生物标志物,并且是其治疗中的新靶标。

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