生物
计算生物学
仿形(计算机编程)
空间分析
蜂窝体系结构
蛋白质组学
桥接(联网)
数字化病理学
肿瘤微环境
生物信息学
建筑
翻译(生物学)
免疫疗法
空间生态学
病理
转移
组织病理学
计算机科学
空间组织
转化研究
疾病
生物标志物
作者
Y J. Li,Z Li,Ryan Quinton,Yuanfeng Ji,Xi Zhang,Jinxi Xiang,Xiyue Wang,Sen Yang,Feyisope Eweje,Yijiang Chen,Xiangde Luo,Y J. Li,Jonathan Mulholland,Siwei Chen,Colin Bergstrom,T Kim,Francesca Olguin,Sierra Willens,S H Lin,Jeffrey Nirschl
出处
期刊:Cell
[Cell Press]
日期:2026-06-16
卷期号:189 (14): 4241-4259.e9
标识
DOI:10.1016/j.cell.2026.05.031
摘要
The tumor microenvironment (TME) critically shapes disease progression and therapeutic resistance. However, a comprehensive understanding of its spatial architecture remains elusive, and clinical translation is challenging. Here, we present cellular architecture and neighborhood-informed virtual AI-driven spatial profiling (CANVAS), an artificial intelligence platform that infers tumor ecological habitats from hematoxylin and eosin (H&E) histopathology. Built on an atlas of over 18 million cells profiled by 41-plex spatial proteomics across 457 patients with non-small cell lung cancer, CANVAS establishes 10 reproducible cellular neighborhoods (CNs) capturing conserved spatial organization of the TME. Through multimodal alignment and foundation-model-based morphological encoding, CANVAS predicts CN-anchored habitat structures from H&E slides and enables clinical evaluation in over 5,000 patients spanning 9 cancer types. Across patient cohorts, CANVAS supports prognostic modeling, spatial ecotype stratification, and immunotherapy outcome prediction. These results establish CANVAS as a clinically scalable platform for spatial profiling, bridging single-cell analysis to population-level insight and enabling precision oncology.
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