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人类疾病中的糖组学及其在生物标志物发现中的新兴作用。

Glycomics in Human Diseases and Its Emerging Role in Biomarker Discovery.

作者信息

Onigbinde Sherifdeen, Adeniyi Moyinoluwa, Daramola Oluwatosin, Chukwubueze Favour, Bhuiyan Md Mostofa Al Amin, Nwaiwu Judith, Bhattacharjee Tuli, Mechref Yehia

机构信息

Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA.

出版信息

Biomedicines. 2025 Aug 21;13(8):2034. doi: 10.3390/biomedicines13082034.

Abstract

Glycosylation, the enzymatic addition of glycans to proteins and lipids, is a critical post-translational modification that influences protein folding, stability, trafficking, immune modulation, and cell signaling. The vast structural diversity of glycans arising from differences in monosaccharide composition, branching, and terminal modifications such as sialylation, fucosylation, and sulfation underpins their functional specificity and regulatory capacity. This review provides a comprehensive overview of glycan biosynthesis, with a focus on -glycans, -glycans, glycosaminoglycans (GAGs), and glycolipids. It explores their essential roles in maintaining cellular homeostasis, development, and immune surveillance. In health, glycans mediate cell-cell communication, protein interactions, and immune responses. In disease, however, aberrant glycosylation is increasingly recognized as a hallmark of numerous pathological conditions, including cancer, neurodegenerative disorders, autoimmune diseases, and a wide range of infectious diseases. Glycomic alterations contribute to tumor progression, immune evasion, therapy resistance, neuroinflammation, and synaptic dysfunction. Tumor-associated carbohydrate antigens (TACAs) and disease-specific glycoforms present novel opportunities for biomarker discovery and therapeutic targeting. Moreover, glycan-mediated host-pathogen interactions are central to microbial adhesion, immune escape, and virulence. This review highlights current advances in glycomics technologies, including mass spectrometry, lectin microarrays, and glycoengineering, which have enabled the high-resolution profiling of the glycome. It also highlights the emerging potential of single-cell glycomics and multi-omics integration in precision medicine. Understanding glycome and its dynamic regulation is essential for uncovering the molecular mechanisms of disease and translating glycomic insights into innovative diagnostic and therapeutic strategies.

摘要

糖基化是指通过酶将聚糖添加到蛋白质和脂质上的过程,是一种关键的翻译后修饰,它会影响蛋白质折叠、稳定性、运输、免疫调节和细胞信号传导。由于单糖组成、分支以及诸如唾液酸化、岩藻糖基化和硫酸化等末端修饰的差异而产生的聚糖结构多样性极大,这支撑了它们的功能特异性和调节能力。本综述全面概述了聚糖生物合成,重点关注N-聚糖、O-聚糖、糖胺聚糖(GAG)和糖脂。它探讨了它们在维持细胞稳态、发育和免疫监视中的重要作用。在健康状态下,聚糖介导细胞间通讯、蛋白质相互作用和免疫反应。然而,在疾病中,异常糖基化越来越被认为是多种病理状况的标志,包括癌症、神经退行性疾病、自身免疫性疾病以及多种传染病。糖组改变会导致肿瘤进展、免疫逃逸、治疗抗性、神经炎症和突触功能障碍。肿瘤相关碳水化合物抗原(TACA)和疾病特异性糖型为生物标志物发现和治疗靶点提供了新的机会。此外,聚糖介导的宿主-病原体相互作用对于微生物粘附、免疫逃逸和毒力至关重要。本综述强调了糖组学技术的当前进展,包括质谱分析、凝集素微阵列和糖工程,这些技术能够对糖组进行高分辨率分析。它还强调了单细胞糖组学和多组学整合在精准医学中的新兴潜力。了解糖组及其动态调节对于揭示疾病的分子机制以及将糖组学见解转化为创新的诊断和治疗策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cc2/12383619/7a0164298869/biomedicines-13-02034-g004.jpg

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