Wang Jun, Shen Tian-Hua, Liu Jie, Wen Qian, Yang Xian-Yan, Deng Yun, Duan Jiang-Jie, Yu Shi-Cang
Department of Stem Cell and Regenerative Medicine, Institute of Pathology and Southwest Cancer Center, Southwest Hospital, Chongqing, 400038, China; International Joint Research Center for Precision Biotherapy, Ministry of Science and Technology, Chongqing, 400038, China; Key Laboratory of Cancer Immunopathology, Ministry of Education, Chongqing, 400038, China; Jin-feng Laboratory, Chongqing, 401329, China.
Department of Stem Cell and Regenerative Medicine, Institute of Pathology and Southwest Cancer Center, Southwest Hospital, Chongqing, 400038, China; International Joint Research Center for Precision Biotherapy, Ministry of Science and Technology, Chongqing, 400038, China; Key Laboratory of Cancer Immunopathology, Ministry of Education, Chongqing, 400038, China.
Cancer Lett. 2025 Sep 28;628:217843. doi: 10.1016/j.canlet.2025.217843. Epub 2025 May 30.
The intricate interplay between neurons and gliomas has emerged as an important area of investigation in glioma biology. Accumulating evidence underscores that structural and material alterations constitute the fundamental basis of neuron‒glioma interactions and their pathological consequences. This review comprehensively examines the mechanisms underlying these interactions, with a particular emphasis on specialized structures that facilitate neuron‒glioma communication, including synapses, cell surface ion channels, and tumor microtubules (TMs). In addition to classical neurotransmitters, we highlight the exchange of cytokines, proteins, and extracellular vesicles (EVs) between these cell types. By synthesizing current research findings, this review establishes a conceptual framework for developing innovative therapeutic strategies targeting neuron‒glioma interfaces, offering new perspectives for glioma treatment approaches.
神经元与胶质瘤之间复杂的相互作用已成为胶质瘤生物学研究的一个重要领域。越来越多的证据表明,结构和物质改变构成了神经元与胶质瘤相互作用及其病理后果的基本基础。本综述全面探讨了这些相互作用的潜在机制,特别强调了促进神经元与胶质瘤交流的特殊结构,包括突触、细胞表面离子通道和肿瘤微管(TMs)。除了经典神经递质外,我们还强调了这些细胞类型之间细胞因子、蛋白质和细胞外囊泡(EVs)的交换。通过综合当前的研究结果,本综述建立了一个针对神经元与胶质瘤界面开发创新治疗策略的概念框架,为胶质瘤治疗方法提供了新的视角。