Dynamic changes in glioma macrophage populations after radiotherapy reveal CSF-1R inhibition as a strategy to overcome resistance
- PMID: 32669424
- DOI: 10.1126/scitranslmed.aaw7843
Dynamic changes in glioma macrophage populations after radiotherapy reveal CSF-1R inhibition as a strategy to overcome resistance
Abstract
Tumor-associated macrophages (TAMs) and microglia (MG) are potent regulators of glioma development and progression. However, the dynamic alterations of distinct TAM populations during the course of therapeutic intervention, response, and recurrence have not yet been fully explored. Here, we investigated how radiotherapy changes the relative abundance and phenotypes of brain-resident MG and peripherally recruited monocyte-derived macrophages (MDMs) in glioblastoma. We identified radiation-specific, stage-dependent MG and MDM gene expression signatures in murine gliomas and confirmed altered expression of several genes and proteins in recurrent human glioblastoma. We found that targeting these TAM populations using a colony-stimulating factor-1 receptor (CSF-1R) inhibitor combined with radiotherapy substantially enhanced survival in preclinical models. Our findings reveal the dynamics and plasticity of distinct macrophage populations in the irradiated tumor microenvironment, which has translational relevance for enhancing the efficacy of standard-of-care treatment in gliomas.
Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.
Comment in
-
CSF1R Inhibitor Prevents Glioblastoma Recurrence.Cancer Discov. 2020 Oct;10(10):OF1. doi: 10.1158/2159-8290.CD-NB2020-078. Epub 2020 Aug 21. Cancer Discov. 2020. PMID: 32826234
Similar articles
-
CSF-1R inhibition alters macrophage polarization and blocks glioma progression.Nat Med. 2013 Oct;19(10):1264-72. doi: 10.1038/nm.3337. Epub 2013 Sep 22. Nat Med. 2013. PMID: 24056773 Free PMC article.
-
The tumor microenvironment underlies acquired resistance to CSF-1R inhibition in gliomas.Science. 2016 May 20;352(6288):aad3018. doi: 10.1126/science.aad3018. Science. 2016. PMID: 27199435 Free PMC article.
-
Colony stimulating factor 1 receptor inhibition delays recurrence of glioblastoma after radiation by altering myeloid cell recruitment and polarization.Neuro Oncol. 2016 Jun;18(6):797-806. doi: 10.1093/neuonc/nov272. Epub 2015 Nov 3. Neuro Oncol. 2016. PMID: 26538619 Free PMC article.
-
The diversity and dynamics of tumor-associated macrophages in recurrent glioblastoma.Front Immunol. 2023 Sep 4;14:1238233. doi: 10.3389/fimmu.2023.1238233. eCollection 2023. Front Immunol. 2023. PMID: 37731483 Free PMC article. Review.
-
Macrophage exclusion after radiation therapy (MERT): A new and effective way to increase the therapeutic ratio of radiotherapy.Radiother Oncol. 2020 Mar;144:159-164. doi: 10.1016/j.radonc.2019.11.020. Epub 2019 Dec 5. Radiother Oncol. 2020. PMID: 31812931 Review.
Cited by
-
Targeting macrophages: a novel treatment strategy in solid tumors.J Transl Med. 2022 Dec 12;20(1):586. doi: 10.1186/s12967-022-03813-w. J Transl Med. 2022. PMID: 36510315 Free PMC article. Review.
-
Immunosuppressive cells in cancer: mechanisms and potential therapeutic targets.J Hematol Oncol. 2022 May 18;15(1):61. doi: 10.1186/s13045-022-01282-8. J Hematol Oncol. 2022. PMID: 35585567 Free PMC article. Review.
-
Tumor-associated macrophage-related strategies for glioma immunotherapy.NPJ Precis Oncol. 2023 Aug 19;7(1):78. doi: 10.1038/s41698-023-00431-7. NPJ Precis Oncol. 2023. PMID: 37598273 Free PMC article. Review.
-
TAMs in Brain Metastasis: Molecular Signatures in Mouse and Man.Front Immunol. 2021 Sep 3;12:716504. doi: 10.3389/fimmu.2021.716504. eCollection 2021. Front Immunol. 2021. PMID: 34539650 Free PMC article. Review.
-
Exosome-transmitted podoplanin promotes tumor-associated macrophage-mediated immune tolerance in glioblastoma.CNS Neurosci Ther. 2024 Mar;30(3):e14643. doi: 10.1111/cns.14643. CNS Neurosci Ther. 2024. PMID: 38470096 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous