The Metabolic Control of Myeloid Cells in the Tumor Microenvironment

被引:5
|
作者
Ramel, Eloise [1 ]
Lillo, Sebastian [1 ]
Daher, Boutaina [2 ]
Fioleau, Marina [1 ]
Daubon, Thomas [2 ]
Saleh, Maya [1 ,3 ]
机构
[1] Univ Bordeaux, CNRS, ImmunoConcEpT, UMR 5164, F-33000 Bordeaux, France
[2] Univ Bordeaux, Inst Biochim & Genet Cellulaires IBGC, CNRS, UMR 5095, F-33000 Bordeaux, France
[3] McGill Univ, Dept Med, Montreal, PQ H3G 0B1, Canada
关键词
cellular metabolism; immunometabolism; myeloid cells; macrophages; tumor microenvironment; cancer; immunotherapy; SUPPRESSOR-CELLS; ALTERNATIVE ACTIVATION; AEROBIC GLYCOLYSIS; MACROPHAGES; EXPRESSION; ADENOSINE; POLARIZATION; HIF-1-ALPHA; CHECKPOINT; INHIBITION;
D O I
10.3390/cells10112960
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Myeloid cells are a key determinant of tumor progression and patient outcomes in a range of cancers and are therefore being actively pursued as targets of new immunotherapies. The recent use of high-dimensional single-cell approaches, e.g., mass cytometry and single-cell RNA-sequencing (scRNA-seq) has reinforced the predominance of myeloid cells in the tumor microenvironment and uncovered their phenotypic diversity in different cancers. The cancerous metabolic environment has emerged as a critical modulator of myeloid cell functions in anti-tumor immunity versus immune suppression and immune evasion. Here, we discuss mechanisms of immune-metabolic crosstalk in tumorigenesis, with a particular focus on the tumor-associated myeloid cell's metabolic programs. We highlight the impact of several metabolic pathways on the pro-tumoral functions of tumor-associated macrophages and myeloid-derived suppressor cells and discuss the potential myeloid cell metabolic checkpoints for cancer immunotherapy, either as monotherapies or in combination with other immunotherapies.
引用
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页数:16
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