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基于神经节苷脂 GM3 的抗癌疫苗:机制与现行策略综述。

Ganglioside GM3-based anticancer vaccines: Reviewing the mechanism and current strategies.

机构信息

Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, UMR 8232, 4 Place Jussieu, Paris 75005, France; College of Life Sciences, Northwest University, Xi'an 710069, China.

Drug Sciences Department, University of Pavia, Viale Taramelli 12, Pavia 27100, Italy.

出版信息

Biomed Pharmacother. 2024 Jul;176:116824. doi: 10.1016/j.biopha.2024.116824. Epub 2024 May 30.

Abstract

Ganglioside GM3 is one of the most common membrane-bound glycosphingolipids. The over-expression of GM3 on tumor cells makes it defined as a tumor-associated carbohydrate antigen (TACA). The specific expression property in cancers, especially in melanoma, make it become an important target to develop anticancer vaccines or immunotherapies. However, in the manner akin to most TACAs, GM3 is an autoantigen facing with problems of low immunogenicity and easily inducing immunotolerance, which means itself only cannot elicit a powerful enough immune response to prevent or treat cancer. With a comparative understanding of the mechanisms that how immune system responses to the carbohydrate vaccines, this review summarizes the studies on the recent efforts to development GM3-based anticancer vaccines.

摘要

神经节苷脂 GM3 是最常见的膜结合糖脂之一。GM3 在肿瘤细胞上的过度表达使其被定义为肿瘤相关碳水化合物抗原 (TACA)。其在癌症中的特异性表达特性,特别是在黑色素瘤中,使其成为开发抗癌疫苗或免疫疗法的重要靶点。然而,与大多数 TACA 一样,GM3 是一种自身抗原,存在免疫原性低和易诱导免疫耐受的问题,这意味着它本身不能引发足够强大的免疫反应来预防或治疗癌症。通过对免疫系统如何对碳水化合物疫苗产生反应的机制的比较了解,本综述总结了基于 GM3 的抗癌疫苗的最新研究进展。

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