胶质瘤
癌症研究
免疫系统
生物
间充质干细胞
表皮生长因子受体
肿瘤微环境
恶性转化
病理
免疫学
受体
细胞生物学
医学
遗传学
作者
Yiyun Chen,Ran Huo,Weirong Kang,Yuwei Liu,Zheng Zhao,Weilun Fu,Ruochen Ma,Xiaomeng Zhang,Jihong Tang,Zhi‐Han Zhu,Qingyang Lyu,Yi Huang,Mengli Yan,Biaobin Jiang,Ruichao Chai,Zhaoshi Bao,Zheng Hu,Weiping Wang,Tao Jiang,Yong Cao
标识
DOI:10.1016/j.xcrm.2023.101177
摘要
) and marking worse prognosis (p = 0.004 and 0.032 in two cohorts). Evolutionary analysis of initial-recurrent glioma pairs and single-cell study of a multi-centric glioblastoma reveal association between elevated TAMo and glioma mesenchymal transformation. Further analyses identify FOSL2 as a TAMo master regulator and demonstrates that FOSL2-EREG/AREG-EGFR signaling axis promotes glioma invasion in vitro. Collectively, we identify TAMo in tumor microenvironment and reveal its driving role in activating EGFR signaling to shape glioma evolution.
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