类有机物
计算机科学
多细胞生物
神经科学
接口(物质)
机制(生物学)
药物发现
癌症治疗
钥匙(锁)
计算神经科学
解码方法
神经生理学
调节器
计算生物学
微流控
轴突引导
生物
人机交互
计算模型
纳米技术
神经活动
神经系统
人工智能
炸薯条
大数据
仿生学
人诱导多能干细胞
诱导多能干细胞
作者
Junlei Han,Fanwei Meng,Jiemeng Ding,Jun Chen,Li Wang,Chaoyang Shi
摘要
ABSTRACT The nervous system is emerging as a central regulator of tumor initiation, progression, and therapeutic response. However, the dynamic mechanisms linking neural activity to malignant, immune, and barrier states remain difficult to dissect in vivo. Animal models capture key aspects of cancer neuroscience, but poorly control human‐specific multicellular interfaces, neural activity, secreted signals, and real‐time readouts. AI‐enabled organoid chip platforms offer a complementary route to reconstruct and interrogate the nerve‐tumor interface by integrating human‐derived organoids, microfluidic control, sensing, and computational modeling. Here we review advances in nerve‐tumor organoids and integrate relevant progress in microfluidics, in situ functional sensing, and AI‐driven modeling. These systems can enable controlled studies of perineural invasion, nerve‐mediated immune regulation, trans‐barrier drug responses, and longitudinal functional states. Key challenges include model standardization, long‐term stability, multimodal data interpretation, and clinical translation. AI‐enabled organoid chip platforms could help shift cancer neuroscience from descriptive observation towards perturbable, human‐relevant and data‐rich systems for mechanism discovery and precision therapy assessment.
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