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
收藏
页数:16
相关论文
共 50 条
  • [41] The tumor microenvironment as a metabolic barrier to effector T cells and immunotherapy
    Lim, Aaron R.
    Rathmell, W. Kimryn
    Rathmell, Jeffrey C.
    ELIFE, 2020, 9 : 1 - 13
  • [42] Tumor-derived exosomes, myeloid-derived suppressor cells, and tumor microenvironment
    Xinyu Tian
    Han Shen
    Zhiyang Li
    Tingting Wang
    Shengjun Wang
    Journal of Hematology & Oncology, 12
  • [43] The Tumor Microenvironment-A Metabolic Obstacle to NK Cells' Activity
    Domagala, Joanna
    Lachota, Mieszko
    Klopotowska, Marta
    Graczyk-Jarzynka, Agnieszka
    Domagala, Antoni
    Zhylko, Andriy
    Soroczynska, Karolina
    Winiarska, Magdalena
    CANCERS, 2020, 12 (12) : 1 - 36
  • [44] Tumor-derived exosomes, myeloid-derived suppressor cells, and tumor microenvironment
    Tian, Xinyu
    Shen, Han
    Li, Zhiyang
    Wang, Tingting
    Wang, Shengjun
    JOURNAL OF HEMATOLOGY & ONCOLOGY, 2019, 12 (01)
  • [45] Tumor microenvironment, histone modifications, and myeloid-derived suppressor cells
    Tian, Xinyu
    Wang, Ting
    Shen, Han
    Wang, Shengjun
    CYTOKINE & GROWTH FACTOR REVIEWS, 2023, 74 : 108 - 121
  • [46] Myeloid-derived suppressor cells in the tumor microenvironment: expect the unexpected
    Marvel, Douglas
    Gabrilovich, Dmitry I.
    JOURNAL OF CLINICAL INVESTIGATION, 2015, 125 (09): : 3356 - 3364
  • [47] Allies or Enemies-The Multifaceted Role of Myeloid Cells in the Tumor Microenvironment
    Haas, Lisa
    Obenauf, Anna C.
    FRONTIERS IN IMMUNOLOGY, 2019, 10
  • [48] The interplay between tumor cells, cancer associated fibroblasts, and immature myeloid cells in the esophageal tumor microenvironment
    Karakasheva, Tatiana
    Lin, Eric
    Hicks, Phil
    Waldron, Todd
    Rustgi, Anil K.
    CANCER RESEARCH, 2016, 76
  • [49] Expansion and functions of myeloid-derived suppressor cells in the tumor microenvironment
    Qu, Peng
    Wang, Li-zhen
    Lin, P. Charles
    CANCER LETTERS, 2016, 380 (01) : 253 - 256
  • [50] Novel Characterization of Myeloid-Derived Suppressor Cells in Tumor Microenvironment
    Li, Yanan
    He, Hongdan
    Jihu, Ribu
    Zhou, Junfu
    Zeng, Rui
    Yan, Hengxiu
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9