Neuro-tumor interactions in peripheral tumors.

IF 8.7
Xueshiyu Ma, Peixuan Ji, Jiahao Zheng, Shuqi Cai, Kan Xu, Yongwei Sun, Dejun Liu
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引用次数: 0

Abstract

The nervous system is now recognized as a pivotal regulator of cancer, marking a paradigm shift that recasts nerves from passive bystanders to active drivers within the tumor microenvironment (TME). This review defines the "neural niche," differentiating passive perineural invasion (PNI) from active tumor innervation. We examine how sympathetic signaling drives an "angio-metabolic switch" and immune evasion, whereas parasympathetic inputs exert context-dependent control over stemness and inflammation. We also highlight the underappreciated role of sensory neurons in promoting T-cell exhaustion via neuropeptides like calcitonin gene-related peptide (CGRP). Finally, we assess therapeutic strategies targeting neural dependence-from repurposing β-blockers to deploying nanotechnologies. Targeting neuro-tumor crosstalk offers a promising strategy to overcome therapeutic resistance and restore anti-tumor immunity.

外周肿瘤中的神经肿瘤相互作用。
神经系统现在被认为是癌症的关键调节器,标志着范式转变,将神经从肿瘤微环境(TME)中的被动旁观者重塑为主动驱动者。这篇综述定义了“神经龛”,区分被动神经周围浸润(PNI)和主动肿瘤神经支配。我们研究了交感神经信号如何驱动“血管代谢开关”和免疫逃避,而副交感神经输入对干性和炎症施加上下文依赖的控制。我们还强调了感觉神经元通过降钙素基因相关肽(CGRP)等神经肽促进t细胞衰竭的作用。最后,我们评估了针对神经依赖性的治疗策略-从重新利用β受体阻滞剂到部署纳米技术。靶向神经肿瘤串扰为克服治疗耐药性和恢复抗肿瘤免疫提供了一种很有前途的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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