Department of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
National & Local Joint Engineering Research Centre of Orthopaedic Biomaterials, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Front Immunol. 2023 Jul 14;14:1202436. doi: 10.3389/fimmu.2023.1202436. eCollection 2023.
Recent scientific reports have revealed a close association between ferroptosis and the occurrence and development of osteoarthritis (OA). Nevertheless, the precise mechanisms by which ferroptosis influences OA and how to hobble OA progression by inhibiting chondrocyte ferroptosis have not yet been fully elucidated. This study aims to conduct a comprehensive systematic review (SR) to address these gaps.
Following the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020, we conducted a comprehensive search of the Embase, Ovid, ProQuest, PubMed, Scopus, the Cochrane Library, and Web of Science databases to identify relevant studies that investigate the association between ferroptosis and chondrocytes in OA. Our search included studies published from the inception of these databases until January 31st, 2023. Only studies that met the predetermined quality criteria were included in this SR.
In this comprehensive SR, a total of 21 studies that met the specified criteria were considered suitable and included in the current updated synthesis. The mechanisms underlying chondrocyte ferroptosis and its association with OA progression involve various biological phenomena, including mitochondrial dysfunction, dysregulated iron metabolism, oxidative stress, and crucial signaling pathways.
Ferroptosis in chondrocytes has opened an entirely new chapter for the investigation of OA, and targeted regulation of it is springing up as an attractive and promising therapeutic tactic for OA.
https://inplasy.com/inplasy-2023-3-0044/, identifier INPLASY202330044.
最近的科学报告揭示了铁死亡与骨关节炎(OA)的发生和发展之间的密切关联。然而,铁死亡影响 OA 的具体机制以及如何通过抑制软骨细胞铁死亡来阻碍 OA 进展尚未完全阐明。本研究旨在进行全面的系统评价(SR)来解决这些空白。
根据 2020 年系统评价和荟萃分析的首选报告项目(PRISMA)指南,我们全面搜索了 Embase、Ovid、ProQuest、PubMed、Scopus、Cochrane 图书馆和 Web of Science 数据库,以确定研究铁死亡与 OA 中软骨细胞之间关系的相关研究。我们的搜索包括从这些数据库创建开始到 2023 年 1 月 31 日发表的研究。只有符合预定质量标准的研究才被纳入本 SR。
在本次全面的 SR 中,共有 21 项符合规定标准的研究被认为是合适的,并纳入了本次更新的综合分析。软骨细胞铁死亡的机制及其与 OA 进展的关系涉及各种生物学现象,包括线粒体功能障碍、铁代谢失调、氧化应激和关键信号通路。
软骨细胞中的铁死亡为 OA 的研究开辟了全新的篇章,靶向调节铁死亡作为一种有吸引力和有前途的 OA 治疗策略正在兴起。
https://inplasy.com/inplasy-2023-3-0044/,标识符 INPLASY202330044。