免疫系统
生物
癌细胞
表型
肿瘤微环境
免疫
细胞生物学
CD8型
癌症
肿瘤进展
代谢途径
癌症研究
免疫学
新陈代谢
遗传学
生物化学
基因
作者
Silvia Cadenas-De Miguel,Giulia Lucianer,Ilaria Elia
标识
DOI:10.1016/j.tibs.2023.03.004
摘要
The metabolic cross-talk between cancer cells and T cells dictates cancer formation and progression. These cells possess metabolic plasticity. Thus, they adapt their metabolic profile to meet their phenotypic requirements. However, the nutrient microenvironment of a tumor is a very hostile niche in which these cells are forced to compete for the available nutrients. The hyperactive metabolism of tumor cells often outcompetes the antitumorigenic CD8+ T cells while promoting the protumorigenic exhausted CD8+ T cells and T regulatory (Treg) cells. Thus, cancer cells elude the immune response and spread in an uncontrolled manner. Identifying the metabolic pathways necessary to shift the balance from a protumorigenic to an antitumorigenic immune phenotype is essential to potentiate antitumor immunity.
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