Nucleic acid aptamers in orthopedic diseases: promising therapeutic agents for bone disorders

IF 15 1区 医学 Q1 CELL & TISSUE ENGINEERING
Zhenhong He, Qingping Peng, Wenying Bin, Luyao Zhao, Yihuang Chen, Yuanqun Zhang, Weihu Yang, Xingchen Yan, Huan Liu
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Abstract

Precision medicine has become a cornerstone in modern therapeutic strategies, with nucleic acid aptamers emerging as pivotal tools due to their unique properties. These oligonucleotide fragments, selected through the Systematic Evolution of Ligands by Exponential Enrichment process, exhibit high affinity and specificity toward their targets, such as DNA, RNA, proteins, and other biomolecules. Nucleic acid aptamers offer significant advantages over traditional therapeutic agents, including superior biological stability, minimal immunogenicity, and the capacity for universal chemical modifications that enhance their in vivo performance and targeting precision. In the realm of osseous tissue repair and regeneration, a complex physiological process essential for maintaining skeletal integrity, aptamers have shown remarkable potential in influencing molecular pathways crucial for bone regeneration, promoting osteogenic differentiation and supporting osteoblast survival. By engineering aptamers to regulate inflammatory responses and facilitate the proliferation and differentiation of fibroblasts, these oligonucleotides can be integrated into advanced drug delivery systems, significantly improving bone repair efficacy while minimizing adverse effects. Aptamer-mediated strategies, including the use of siRNA and miRNA mimics or inhibitors, have shown efficacy in enhancing bone mass and microstructure. These approaches hold transformative potential for treating a range of orthopedic conditions like osteoporosis, osteosarcoma, and osteoarthritis. This review synthesizes the molecular mechanisms and biological roles of aptamers in orthopedic diseases, emphasizing their potential to drive innovative and effective therapeutic interventions.

Abstract Image

核酸适体在骨科疾病中的应用:有希望的骨疾病治疗剂
精确医学已成为现代治疗策略的基石,核酸适体因其独特的性质而成为关键工具。这些寡核苷酸片段,通过配体的系统进化,通过指数富集过程选择,对其目标,如DNA, RNA,蛋白质和其他生物分子具有高亲和力和特异性。与传统的治疗药物相比,核酸适体具有显著的优势,包括优越的生物稳定性、最小的免疫原性和普遍化学修饰的能力,从而提高了它们在体内的性能和靶向精度。骨组织修复和再生是维持骨骼完整性所必需的复杂生理过程,适配体在影响骨再生、促进成骨分化和支持成骨细胞存活的关键分子途径方面显示出巨大的潜力。通过设计适体来调节炎症反应,促进成纤维细胞的增殖和分化,这些寡核苷酸可以整合到先进的药物输送系统中,显著提高骨修复效果,同时最大限度地减少不良反应。适配体介导的策略,包括使用siRNA和miRNA模拟物或抑制剂,已显示出增强骨量和微观结构的功效。这些方法在治疗骨质疏松、骨肉瘤和骨关节炎等一系列骨科疾病方面具有变革性的潜力。本文综述了适体在骨科疾病中的分子机制和生物学作用,强调了它们在推动创新和有效治疗干预方面的潜力。
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来源期刊
Bone Research
Bone Research CELL & TISSUE ENGINEERING-
CiteScore
20.00
自引率
4.70%
发文量
289
审稿时长
20 weeks
期刊介绍: Established in 2013, Bone Research is a newly-founded English-language periodical that centers on the basic and clinical facets of bone biology, pathophysiology, and regeneration. It is dedicated to championing key findings emerging from both basic investigations and clinical research concerning bone-related topics. The journal's objective is to globally disseminate research in bone-related physiology, pathology, diseases, and treatment, contributing to the advancement of knowledge in this field.
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