Guan Shiyao, Zhang Zhen, Wu Jun
School of Biomedical Engineering, Shenzhen Campus of Sun Yat-sen University, Shenzhen 518107, China.
iScience. 2022 Jul 20;25(8):104807. doi: 10.1016/j.isci.2022.104807. eCollection 2022 Aug 19.
More than 20 million individuals worldwide suffer from congenital or acquired bone defects annually. The development of bone scaffold materials that simulate natural bone for bone defect repair remains challenging. Recently, ncRNA-based therapies for bone defects have attracted increasing interest because of the great potential of ncRNAs in disease treatment. Various types of ncRNAs regulate gene expression in osteogenesis-related cells via multiple mechanisms. The delivery of ncRNAs to the site of bone loss through gene vectors or scaffolds is a potential therapeutic option for bone defect repair. Therefore, this study discusses and summarizes the regulatory mechanisms of miRNAs, siRNAs, and piRNAs in osteogenic signaling and reviews the widely used current RNA delivery vectors and scaffolds for bone defect repair. Additionally, current challenges and potential solutions of delivery scaffolds for bone defect repair are proposed, with the aim of providing a theoretical basis for their future clinical applications.
全球每年有超过2000万人患有先天性或后天性骨缺损。开发模拟天然骨用于骨缺损修复的骨支架材料仍然具有挑战性。近来,基于非编码RNA的骨缺损治疗方法因其在疾病治疗中的巨大潜力而受到越来越多的关注。各种类型的非编码RNA通过多种机制调节成骨相关细胞中的基因表达。通过基因载体或支架将非编码RNA递送至骨丢失部位是骨缺损修复的一种潜在治疗选择。因此,本研究讨论并总结了微小RNA、小干扰RNA和PIWI相互作用RNA在成骨信号传导中的调控机制,并综述了目前广泛用于骨缺损修复的RNA递送载体和支架。此外,还提出了骨缺损修复递送支架目前面临的挑战和潜在解决方案,旨在为其未来的临床应用提供理论依据。