Your browser doesn't support javascript.
loading
Targeting Metabolic Pathways of Myeloid Cells Improves Cancer Immunotherapy.
Li, Jianying; Bolyard, Chelsea; Xin, Gang; Li, Zihai.
Affiliation
  • Li J; Pelotonia Institute of Immuno-Oncology, the Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, Columbus, OH, United States.
  • Bolyard C; Pelotonia Institute of Immuno-Oncology, the Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, Columbus, OH, United States.
  • Xin G; Pelotonia Institute of Immuno-Oncology, the Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, Columbus, OH, United States.
  • Li Z; Department of Microbial Infection and Immunity, the Ohio State University College of Medicine, Columbus, OH, United States.
Front Cell Dev Biol ; 9: 747863, 2021.
Article in En | MEDLINE | ID: mdl-34988072
ABSTRACT
Tumor-infiltrating myeloid cells are a prominent pro-tumorigenic immune cell population that limit host anti-tumor immunity and present a significant obstacle for many cancer immunotherapies. Targeting the mechanisms regulating myeloid cell function within the tumor microenvironment may overcome immunotherapy resistance in some cancers. Recent discoveries in the emerging field of immunometabolism reveal that the metabolic profiles of intratumoral myeloid cells are rewired to adapt to the nutrition-limited tumor microenvironment, and this shapes their pro-tumor phenotypes. Interestingly, metabolic modulation can shift these myeloid cells toward the immune-stimulating anti-tumor phenotype. In this review, we will highlight the roles of specific metabolic pathways in the activation and function of myeloid cells, and discuss the therapeutic value of metabolically reprogramming myeloid cells to augment and improve outcomes with cancer immunotherapy.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2021 Type: Article Affiliation country: United States