Hasan Ahmed, Ardizzone Alessio, Giosa Domenico, Scuderi Sarah Adriana, Calcaterra Elsa, Esposito Emanuela, Capra Anna Paola
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale Ferdinando Stagno D'Alcontres, 31, 98166 Messina, Italy.
Center of Neuroscience, School of Advanced Studies, University of Camerino, 62032 Camerino, Italy.
Curr Issues Mol Biol. 2025 Jan 21;47(2):70. doi: 10.3390/cimb47020070.
Spinal cord injury (SCI) involves complex pathological processes that often result in significant and long-term neurological deficits. Increasingly, research has identified microRNA-21 (miR-21) as a pivotal regulator in SCI, with studies focusing on its roles in inflammation, apoptosis, and tissue repair. This review synthesizes current findings on miR-21's involvement in post-injury molecular events, emphasizing its interactions with regulatory targets such as Phosphatase and Tensin Homolog (PTEN) and Programmed Cell Death Protein 4 (PDCD4), as well as its broader effects on inflammatory and apoptotic signaling pathways. Evidence from both in vitro and in vivo studies suggests that modulating miR-21 influences lesion size, cellular dynamics, and functional recovery, highlighting its potential as a therapeutic target for SCI. Nonetheless, the clinical translation of miR-21-based therapies poses significant challenges, including the need to optimize dosages, delivery mechanisms, and long-term safety profiles. Further research is crucial to fully delineate miR-21's therapeutic potential and determine its feasibility for integration into SCI treatment protocols. This review aims to provide a comprehensive overview of miR-21's roles in SCI pathology, offering insights into the molecular mechanisms underlying recovery and the emerging potential of miR-21 in SCI management to enhance outcomes and quality of life for affected patients.
脊髓损伤(SCI)涉及复杂的病理过程,常常导致严重且长期的神经功能缺损。越来越多的研究已将微小RNA - 21(miR - 21)确定为脊髓损伤中的关键调节因子,相关研究聚焦于其在炎症、细胞凋亡和组织修复中的作用。本综述综合了目前关于miR - 21参与损伤后分子事件的研究结果,着重强调了其与诸如磷酸酶和张力蛋白同源物(PTEN)及程序性细胞死亡蛋白4(PDCD4)等调控靶点的相互作用,以及其对炎症和凋亡信号通路的更广泛影响。来自体外和体内研究的证据表明,调节miR - 21会影响损伤大小、细胞动态变化和功能恢复,凸显了其作为脊髓损伤治疗靶点的潜力。尽管如此,基于miR - 21的疗法的临床转化面临重大挑战,包括需要优化剂量、递送机制和长期安全性。进一步的研究对于全面阐明miR - 21的治疗潜力并确定其整合到脊髓损伤治疗方案中的可行性至关重要。本综述旨在全面概述miR - 21在脊髓损伤病理学中的作用,深入了解恢复背后的分子机制以及miR - 21在脊髓损伤管理中的新潜力,以改善受影响患者的治疗效果和生活质量。