生物
成纤维细胞
癌相关成纤维细胞
计算生物学
磷蛋白
功能(生物学)
癌细胞
细胞生物学
高分辨率
肿瘤微环境
超分辨率
利基
表型
空间分析
肿瘤细胞
癌症
低分辨率
癌症治疗
构造(python库)
地图集(解剖学)
分辨率(逻辑)
癌症研究
作者
Xiongfeng Chen,Zhuan Zhou,Luyu Xie,Kailiang Qiao,Yiyue Jia,Si Liu,Zeynep Yazgan,Francesca Rossi,Yang Liu,Bo Zhang,Patricio Marcelo Polanco,Herbert J. Zeh,Alex C. Kim,Huocong Huang
出处
期刊:Cancer Cell
[Cell Press]
日期:2025-09-25
卷期号:43 (12): 2224-2240.e9
被引量:63
标识
DOI:10.1016/j.ccell.2025.09.001
摘要
Recent studies have identified a unique subtype of cancer-associated fibroblasts (CAFs) termed antigen-presenting CAFs (apCAFs), which remain the least understood CAF subtype. To gain a comprehensive understanding of the origin and function apCAFs, we construct a fibroblast molecular atlas across 14 types of solid tumors. Our integration study unexpectedly reveals two distinct apCAF lineages present in most cancer types: one associated with mesothelial-like cells and the other with fibrocytes. Using a high-resolution single-cell spatial imaging platform, we characterize the spatial niches of these apCAF lineages. We find that mesothelial-like apCAFs are located near cancer cells, while fibrocyte-like apCAFs are associated with tertiary lymphoid structures. Additionally, we discover that both apCAF lineages can up-regulate the secreted protein SPP1, which facilitates primary tumor formation and peritoneal metastasis. Taken together, this study offers an unprecedented resolution in analyzing apCAF lineages and their spatial niches.
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