Regulation of gut microbiota on immune cell ferroptosis: A novel insight for immunotherapy against tumor

免疫系统 免疫疗法 肠道菌群 免疫学 生物 肿瘤免疫学 癌症研究
作者
Ruobing Liu,Juanjuan Wang,Yuqing Liu,Yunhuan Gao,Rongcun Yang
出处
期刊:Cancer Letters [Elsevier]
卷期号:: 217115-217115
标识
DOI:10.1016/j.canlet.2024.217115
摘要

Gut microbiota contributes to the homeostasis of immune system and is related to various diseases such as tumorigenesis. Ferroptosis, a new type of cell death, is also involved in the disease pathogenesis. Recent studies have found the correlations of gut microbiota mediated ferroptosis and immune cell death. Gut microbiota derived immunosuppressive metabolites, which can promote differentiation and function of immune cells, tend to inhibit ferroptosis through their receptors, whereas inflammatory metabolites from gut microbiota also affect the differentiation and function of immune cells and their ferroptosis. Thus, it is possible for gut microbiota to regulate immune cell ferroptosis. Indeed, gut microbiota metabolite receptor aryl hydrocarbon receptor (AhR) can affect ferroptosis of intestinal intraepithelial lymphocytes, leading to disease pathogenesis. Since immune cell ferroptosis in tumor microenvironment (TME) affects the occurrence and development of tumor, the modulation of gut microbiota in these cell ferroptosis might influence on the tumorigenesis, and also immunotherapy against tumors. Here we will summarize the recent advance of ferroptosis mediated by gut microbiota metabolites, which potentially acts as regulator(s) on immune cells in TME for therapy against tumor.
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