Cancer cell · 2024
Identification of hypoxic macrophages in glioblastoma with therapeutic potential for vasculature normalization.
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Wang Wenying, Li Tianran, Cheng Yue, Li Fei, Qi Shuhong, Mao Min, Wu Jingjing, Liu Qing, Zhang Xiaoning, Li Xuegang, Zhang Lu, Qi Haoyue, Yang Lan, Yang Kaidi, He Zhicheng, Ding Shuaishuai, Qin Zhongyi, Yang Ying, Yang Xi, Luo Chunhua, Guo Ying, Wang Chao, Liu Xindong, Zhou Lei, Liu Yuqi, Kong Weikai, Miao Jingya, Ye Shuanghui, Luo Min, An Lele, Wang Lujing, Che Linrong, Niu Qin, Ma Qinghua, Zhang Xia, Zhang Zhihong, Hu Rong, Feng Hua, Ping Yi-Fang, Bian Xiu-Wu, Shi Yu
Аннотация
Monocyte-derived tumor-associated macrophages (Mo-TAMs) intensively infiltrate diffuse gliomas with remarkable heterogeneity. Using single-cell transcriptomics, we chart a spatially resolved transcriptional landscape of Mo-TAMs across 51 patients with isocitrate dehydrogenase (IDH)-wild-type glioblastomas or IDH-mutant gliomas. We characterize a Mo-TAM subset that is localized to the peri-necrotic niche and skewed by hypoxic niche cues to acquire a hypoxia response signature. Hypoxia-TAM destabilizes endothelial adherens junctions by activating adrenomedullin paracrine signaling, thereby stimulating a hyperpermeable neovasculature that hampers drug delivery in glioblastoma xenografts. Accordingly, genetic ablation or pharmacological blockade of adrenomedullin produced by Hypoxia-TAM restores vascular integrity, improves intratumoral concentration of the anti-tumor agent dabrafenib, and achieves combinatorial therapeutic benefits. Increased proportion of Hypoxia-TAM or adrenomedullin expression is predictive of tumor vessel hyperpermeability and a worse prognosis of glioblastoma. Our findings highlight Mo-TAM diversity and spatial niche-steered Mo-TAM reprogramming in diffuse gliomas and indicate potential therapeutics targeting Hypoxia-TAM to normalize tumor vasculature.