BACKGROUND: Tumor-associated macrophages have been implicated in the progression and treatment resistance of glioblastoma (GBM). This study aimed to identify macrophage-related genes associated with prognosis and therapeutic response in GBM. MATERIALS AND METHODS: Bulk RNA-seq data from 533 patients with GBM were downloaded from the Cancer Genome Atlas (TCGA) and Chinese Glioma Genome Atlas (CGGA) databases. Bioinformatic tools were used to detect the co-expression gene modules associated with the infiltration of immune cells, identify a prognostic macrophage-related gene signature, and explore their association with sensitivity to chemotherapeutic drugs and immune checkpoint blockade. Single-cell RNA-seq data and multiplexed immunofluorescence were used to validate ISG20 expression (a member of the identified gene signature) in macrophages. RESULTS: We detected gene modules associated with macrophages and identified a signature consisting of three macrophage-related genes (ISG20, PARP12 and IFIT5) in the discovery set (TCGA-GBM, nâ=â159), and validated its prognostic value in the validation set (CGGA-GBM, nâ=â374). This gene signature demonstrated favorable accuracy in predicting prognosis and resistance of immuno- and chemo-therapy. The co-expression of ISG20 and PD-1 in macrophages was verified by single-cell RNA-seq data and multiplex immunofluorescence. CONCLUSIONS: This study presents a macrophage-related gene signature to predict prognosis and therapeutic response in GBM. ISG20, PARP12 and IFIT5 are interferon-stimulated genes, and further investigations may provide new insights into the interplay between macrophages and interferon signaling in GBM.
Identification of a prognostic signature consisting of three macrophage-related genes for glioblastoma based on bulk and single-cell transcriptomes analyses.
基于整体和单细胞转录组分析,鉴定出由三个巨噬细胞相关基因组成的胶质母细胞瘤预后特征
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作者:Wu Qiyan, Chen Chuanbiao, Li Lina, Liu Hongyu, Cui Lingling, Bai Yang, Zhang Liping, Wang Lingxiong, Peng Yaojun
| 期刊: | Annals of Medicine | 影响因子: | 4.300 |
| 时间: | 2025 | 起止号: | 2025 Dec;57(1):2546111 |
| doi: | 10.1080/07853890.2025.2546111 | 研究方向: | 细胞生物学 |
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