Macrophages in Glioblastoma Development and Therapy: A Double-Edged Sword

Glioblastoma (GBM) is one of the leading lethal tumors, featuring aggressive malignancy and poor outcome to current standard temozolomide (TMZ) or radio-based therapy. Developing immunotherapies, especially immune checkpoint inhibitors, have improved patient outcomes in other solid tumors but remain...

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Main Authors: Mengwan Wu, Ying Shi, Luyi Zhu, Luoyi Chen, Xinchen Zhao, Chuan Xu
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Life
Subjects:
Online Access:https://www.mdpi.com/2075-1729/12/8/1225
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author Mengwan Wu
Ying Shi
Luyi Zhu
Luoyi Chen
Xinchen Zhao
Chuan Xu
author_facet Mengwan Wu
Ying Shi
Luyi Zhu
Luoyi Chen
Xinchen Zhao
Chuan Xu
author_sort Mengwan Wu
collection DOAJ
description Glioblastoma (GBM) is one of the leading lethal tumors, featuring aggressive malignancy and poor outcome to current standard temozolomide (TMZ) or radio-based therapy. Developing immunotherapies, especially immune checkpoint inhibitors, have improved patient outcomes in other solid tumors but remain fatigued in GBM patients. Emerging evidence has shown that GBM-associated macrophages (GAMs), comprising brain-resident microglia and bone marrow-derived macrophages, act critically in boosting tumor progression, altering drug resistance, and establishing an immunosuppressive environment. Based on its crucial role, evaluations of the safety and efficacy of GAM-targeted therapy are ongoing, with promising (pre)clinical evidence updated. In this review, we summarized updated literature related to GAM nature, the interplay between GAMs and GBM cells, and GAM-targeted therapeutic strategies.
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spelling doaj.art-78c54351e2f64304a5fcff2dd4d890272023-12-03T13:58:55ZengMDPI AGLife2075-17292022-08-01128122510.3390/life12081225Macrophages in Glioblastoma Development and Therapy: A Double-Edged SwordMengwan Wu0Ying Shi1Luyi Zhu2Luoyi Chen3Xinchen Zhao4Chuan Xu5Integrative Cancer Center & Cancer Clinical Research Center, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, ChinaIntegrative Cancer Center & Cancer Clinical Research Center, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, ChinaIntegrative Cancer Center & Cancer Clinical Research Center, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, ChinaIntegrative Cancer Center & Cancer Clinical Research Center, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, ChinaIntegrative Cancer Center & Cancer Clinical Research Center, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, ChinaIntegrative Cancer Center & Cancer Clinical Research Center, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, ChinaGlioblastoma (GBM) is one of the leading lethal tumors, featuring aggressive malignancy and poor outcome to current standard temozolomide (TMZ) or radio-based therapy. Developing immunotherapies, especially immune checkpoint inhibitors, have improved patient outcomes in other solid tumors but remain fatigued in GBM patients. Emerging evidence has shown that GBM-associated macrophages (GAMs), comprising brain-resident microglia and bone marrow-derived macrophages, act critically in boosting tumor progression, altering drug resistance, and establishing an immunosuppressive environment. Based on its crucial role, evaluations of the safety and efficacy of GAM-targeted therapy are ongoing, with promising (pre)clinical evidence updated. In this review, we summarized updated literature related to GAM nature, the interplay between GAMs and GBM cells, and GAM-targeted therapeutic strategies.https://www.mdpi.com/2075-1729/12/8/1225glioblastomamacrophagemicrogliaimmunotherapytargeted therapy
spellingShingle Mengwan Wu
Ying Shi
Luyi Zhu
Luoyi Chen
Xinchen Zhao
Chuan Xu
Macrophages in Glioblastoma Development and Therapy: A Double-Edged Sword
Life
glioblastoma
macrophage
microglia
immunotherapy
targeted therapy
title Macrophages in Glioblastoma Development and Therapy: A Double-Edged Sword
title_full Macrophages in Glioblastoma Development and Therapy: A Double-Edged Sword
title_fullStr Macrophages in Glioblastoma Development and Therapy: A Double-Edged Sword
title_full_unstemmed Macrophages in Glioblastoma Development and Therapy: A Double-Edged Sword
title_short Macrophages in Glioblastoma Development and Therapy: A Double-Edged Sword
title_sort macrophages in glioblastoma development and therapy a double edged sword
topic glioblastoma
macrophage
microglia
immunotherapy
targeted therapy
url https://www.mdpi.com/2075-1729/12/8/1225
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AT luoyichen macrophagesinglioblastomadevelopmentandtherapyadoubleedgedsword
AT xinchenzhao macrophagesinglioblastomadevelopmentandtherapyadoubleedgedsword
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