Mao Xingjia, Cao Yanyan, Guo Zijian, Wang Linlin, Xiang Chuan
Department of Orthopedics, The Second Hospital of Shanxi Medical University, Taiyuan 030000, China.
MicroNano System Research Center, Taiyuan University of Technology, Taiyuan, China.
Mol Ther Nucleic Acids. 2021 May 8;24:856-867. doi: 10.1016/j.omtn.2021.04.006. eCollection 2021 Jun 4.
Osteoarthritis (OA) is a common and disabling joint disorder that is mainly characterized by cartilage degeneration and narrow joint spaces. The regulatory functions of non-coding RNAs (long non-coding RNAs, microRNAs [miRNAs], and circular RNAs [circRNAs]) in OA progression have attracted considerable attention, and the function of circular RNAs in the context of OA has been an increasingly popular research topic in the last 6 years. Recent studies have reported that various circRNAs can delay or aggravate diverse aspects of the OA process, including extracellular matrix formation, apoptosis, proliferation, inflammation, and autophagy, via circRNA/miRNA/mRNA pathways. Thus, circRNAs and related pathways are potential therapeutic targets for OA. Our review provides comprehensive information about circRNAs, including their biogenesis, functions, and characteristics, and it reveals their critical roles in the pathogenesis of OA via a large regulatory network of sponges. Considering their regulatory functions and characteristics, we hypothesize that circRNAs not only can be transferred through bodily fluids to serve as diagnostic biomarkers, but they can also be released from mesenchymal stem cell-derived exosomes and delivered to OA chondrocytes acting as therapeutic circRNAs. Further investigations of the in-depth molecular mechanisms of action of circRNAs in OA are expected to provide effective and safe OA treatment strategies.
骨关节炎(OA)是一种常见的致残性关节疾病,主要特征为软骨退变和关节间隙变窄。非编码RNA(长链非编码RNA、微小RNA[miRNA]和环状RNA[circRNA])在OA进展中的调控功能已引起广泛关注,在过去6年中,circRNA在OA中的功能一直是一个越来越热门的研究课题。最近的研究报道,各种circRNA可通过circRNA/miRNA/mRNA途径延缓或加重OA进程的各个方面,包括细胞外基质形成、细胞凋亡、增殖、炎症和自噬。因此,circRNA及其相关途径是OA潜在的治疗靶点。我们的综述提供了有关circRNA的全面信息,包括其生物发生、功能和特征,并通过一个庞大的海绵调控网络揭示了它们在OA发病机制中的关键作用。考虑到它们的调控功能和特征,我们推测circRNA不仅可以通过体液传递作为诊断生物标志物,还可以从间充质干细胞衍生的外泌体中释放出来,作为治疗性circRNA传递给OA软骨细胞。对circRNA在OA中深入分子作用机制的进一步研究有望提供有效且安全的OA治疗策略。