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唾液酸及唾液酸化在人类健康与疾病中的生物学功能

Biological function of sialic acid and sialylation in human health and disease.

作者信息

Zhu Wengen, Zhou Yue, Guo Linjuan, Feng Shenghui

机构信息

Department of Cardiology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.

Department of Ophthalmology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

出版信息

Cell Death Discov. 2024 Sep 30;10(1):415. doi: 10.1038/s41420-024-02180-3.

Abstract

Sialic acids are predominantly found at the terminal ends of glycoproteins and glycolipids and play key roles in cellular communication and function. The process of sialylation, a form of post-translational modification, involves the covalent attachment of sialic acid to the terminal residues of oligosaccharides and glycoproteins. This modification not only provides a layer of electrostatic repulsion to cells but also serves as a receptor for various biological signaling pathways. Sialylation is involved in several pathophysiological processes. Given its multifaceted involvement in cellular functions, sialylation presents a promising avenue for therapeutic intervention. Current studies are exploring agents that target sialic acid residues on sialoglycans or the sialylation process. These efforts are particularly focused on the fields of cancer therapy, stroke treatment, antiviral strategies, and therapies for central nervous system disorders. In this review, we aimed to summarize the biological functions of sialic acid and the process of sialylation, explore their roles in various pathophysiological contexts, and discuss their potential applications in the development of novel therapeutics.

摘要

唾液酸主要存在于糖蛋白和糖脂的末端,在细胞通讯和功能中发挥关键作用。唾液酸化过程是一种翻译后修饰形式,涉及唾液酸与寡糖和糖蛋白末端残基的共价连接。这种修饰不仅为细胞提供了一层静电排斥作用,还作为各种生物信号通路的受体。唾液酸化参与了多个病理生理过程。鉴于其在细胞功能中的多方面参与,唾液酸化是一个有前景的治疗干预途径。目前的研究正在探索靶向唾液酸聚糖上唾液酸残基或唾液酸化过程的药物。这些努力特别集中在癌症治疗、中风治疗、抗病毒策略以及中枢神经系统疾病治疗等领域。在本综述中,我们旨在总结唾液酸的生物学功能和唾液酸化过程,探讨它们在各种病理生理背景下的作用,并讨论它们在新型治疗药物开发中的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51ed/11442784/feb0b472836f/41420_2024_2180_Fig1_HTML.jpg

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