Hu Kangyi, Wen Haonan, Song Ting, Che Zhixin, Song Yongjia, Song Min
Clinical College of Traditional Chinese Medicine, Gansu University of Chinese Medicine, Lanzhou, People's Republic of China.
J Inflamm Res. 2024 Sep 20;17:6563-6581. doi: 10.2147/JIR.S489682. eCollection 2024.
Long non-coding RNA (LncRNA), with transcripts over 200 nucleotides in length, play critical roles in numerous biological functions and have emerged as significant players in the pathogenesis of osteoarthritis (OA), an inflammatory condition traditionally viewed as a degenerative joint disease. This review comprehensively examines the influence of LncRNA on the inflammatory processes driving OA progression, focusing on their role in regulating gene expression, cellular activities, and inflammatory pathways. Notably, LncRNAs such as MALAT1, H19, and HOTAIR are upregulated in OA and exacerbate the inflammatory milieu by modulating key signaling pathways like NF-κB, TGF-β/SMAD, and Wnt/β-catenin. Conversely, LncRNA like MEG3 and GAS5, which are downregulated in OA, show potential in dampening inflammatory responses and protecting against cartilage degradation by influencing miRNA interactions and cytokine production. By enhancing our understanding of LncRNA' roles in OA inflammation, we can better leverage them as potential biomarkers for the disease and develop innovative therapeutic strategies for OA management. This paper aims to delineate the mechanisms by which LncRNA influence inflammatory responses in OA and propose them as novel targets for therapeutic intervention.
长链非编码RNA(LncRNA)的转录本长度超过200个核苷酸,在众多生物学功能中发挥着关键作用,并已成为骨关节炎(OA)发病机制中的重要因素。OA是一种传统上被视为退行性关节疾病的炎症性病症。本综述全面研究了LncRNA对驱动OA进展的炎症过程的影响,重点关注它们在调节基因表达、细胞活动和炎症途径中的作用。值得注意的是,诸如MALAT1、H19和HOTAIR等LncRNA在OA中上调,并通过调节NF-κB、TGF-β/SMAD和Wnt/β-连环蛋白等关键信号通路加剧炎症环境。相反,在OA中下调的LncRNA如MEG3和GAS5,通过影响miRNA相互作用和细胞因子产生,在减轻炎症反应和防止软骨降解方面显示出潜力。通过加强我们对LncRNA在OA炎症中作用的理解,我们可以更好地将它们用作该疾病的潜在生物标志物,并开发创新的OA治疗策略。本文旨在阐述LncRNA影响OA炎症反应的机制,并将它们作为治疗干预的新靶点提出。