Lipid-Laden Macrophages Recycle Myelin to Feed Glioblastoma

Tumor-associated microglia and macrophages (TAM) make up the largest immune cell population in the glioblastoma (GBM) tumor microenvironment. Given the heterogeneity and plasticity of TAMs in the GBM tumor microenvironment, understanding the context-dependent cancer cell-TAM symbiotic interaction is crucial for understanding GBM biology and developing effective therapies. In a recent issue of Cell, Kloosterman and colleagues identified a subpopulation of glycoprotein nonmetastatic melanoma protein Bhigh lipid-laden microglia and macrophages (LLM) in GBM. Mesenchymal-like GBM cells help generate the LLM phenotype. Reciprocally, LLMs are epigenetically rewired to recycle myelin and transfer the lipid from myelin to cancer cells, fueling mesenchymal-like GBM progression in a liver X receptor/ABCA1-dependent manner. Together, leveraging LLMs opens new therapeutic possibilities for rewiring the metabolism-mediated tumor-TAM interaction during GBM progression.

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Publication Details

Journal
Cancer Research
Published
2024-09-18
DOI
https://doi.org/10.1158/0008-5472.can-24-3362
Citations
9
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
2.16
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article

Lipid-Laden Macrophages Recycle Myelin to Feed Glioblastoma

Fei Zhou, Lizhi Pang, Peiwen Chen
9 citations
Cancer Research
Immune cells in cancer
2.16
article

Lipid-Laden Macrophages Recycle Myelin to Feed Glioblastoma

Fei Zhou, Lizhi Pang, Peiwen Chen
article en
9 citations

Abstract

Tumor-associated microglia and macrophages (TAM) make up the largest immune cell population in the glioblastoma (GBM) tumor microenvironment. Given the heterogeneity and plasticity of TAMs in the GBM tumor microenvironment, understanding the context-dependent cancer cell-TAM symbiotic interaction is crucial for understanding GBM biology and developing effective therapies. In a recent issue of Cell, Kloosterman and colleagues identified a subpopulation of glycoprotein nonmetastatic melanoma protein Bhigh lipid-laden microglia and macrophages (LLM) in GBM. Mesenchymal-like GBM cells help generate the LLM phenotype. Reciprocally, LLMs are epigenetically rewired to recycle myelin and transfer the lipid from myelin to cancer cells, fueling mesenchymal-like GBM progression in a liver X receptor/ABCA1-dependent manner. Together, leveraging LLMs opens new therapeutic possibilities for rewiring the metabolism-mediated tumor-TAM interaction during GBM progression.

Cancer ResearchVol. 84(22)
Northwestern University (US), Cleveland Clinic (US), Cleveland Clinic Lerner College of Medicine (US)
Good health and well-being
Openalex Percentile: Top 12%
Immune cells in cancer
2.16
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