Ni Ping, Chen Kejie, Xiang Jing, Shao Haifeng, Chen Xiaoling, Chen Qiao, Wang Lingling, Hao Junli, Huang Xinyi, Cao Qing, Yang Yali, Tan Quandan, Yang Jie, Li Suping
School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Department of Neurology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Front Genet. 2025 Sep 8;16:1618105. doi: 10.3389/fgene.2025.1618105. eCollection 2025.
The high incidence and mortality rates of cardiovascular and cerebrovascular diseases make them a significant global health challenge. Antiplatelet drugs play a central role in the prevention and treatment of these diseases. Despite the wide range of available antiplatelet drugs, antiplatelet drug resistance is not rare. So optimizing drug use through personalized treatment strategies to achieve maximum therapeutic benefit remains a major challenge in clinical practice. Non-coding RNAs, including microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), have made significant progress in understanding their regulatory roles in drug resistance, becoming a frontier area of current research. In addition to the regulatory functions of non-coding RNAs, emerging studies have highlighted the role of RNA modifications, such as N6-methyladenosine (m6A), in the regulation of gene expression and cellular processes involved in antiplatelet drug resistance. These modifications contribute to the stability, splicing, and translation of RNA, further influencing their roles in drug resistance mechanisms. In recent years, significant progress has been made in the research of non-coding RNAs and RNA modifications, revealing their crucial roles in the mechanisms of antiplatelet drug resistance. This review focuses on the latest advancements in non-coding RNA research related to antiplatelet drug resistance and explores the emerging field of RNA modifications. It analyzes potential underlying mechanisms and discusses future research directions, aiming to provide new theoretical support and research perspectives for personalized precision antiplatelet.
心血管疾病和脑血管疾病的高发病率和高死亡率使其成为一项重大的全球健康挑战。抗血小板药物在这些疾病的预防和治疗中发挥着核心作用。尽管有多种抗血小板药物可供使用,但抗血小板药物耐药并不罕见。因此,通过个性化治疗策略优化药物使用以实现最大治疗效益仍然是临床实践中的一项重大挑战。非编码RNA,包括微小RNA(miRNA)、长链非编码RNA(lncRNA)和环状RNA(circRNA),在理解其在耐药性中的调控作用方面取得了重大进展,成为当前研究的前沿领域。除了非编码RNA的调控功能外,新兴研究还强调了RNA修饰,如N6-甲基腺苷(m6A),在抗血小板药物耐药相关基因表达调控和细胞过程中的作用。这些修饰有助于RNA的稳定性、剪接和翻译,进一步影响它们在耐药机制中的作用。近年来,非编码RNA和RNA修饰的研究取得了重大进展,揭示了它们在抗血小板药物耐药机制中的关键作用。本综述重点关注与抗血小板药物耐药相关的非编码RNA研究的最新进展,并探索RNA修饰这一新兴领域。分析潜在的作用机制并讨论未来的研究方向,旨在为个性化精准抗血小板治疗提供新的理论支持和研究视角。