肿瘤微环境
巨噬细胞极化
癌症研究
巨噬细胞
生物
NF-κB
癌症免疫疗法
免疫疗法
免疫抑制
表型
炎症
免疫系统
免疫学
基因
体外
遗传学
作者
Jessica Cornice,Daniela Verzella,Paola Arboretto,Davide Vecchiotti,Daria Capece,Francesca Zazzeroni,Guido Franzoso
出处
期刊:Genes
[MDPI AG]
日期:2024-01-31
卷期号:15 (2): 197-197
被引量:11
标识
DOI:10.3390/genes15020197
摘要
Tumor-associated macrophages (TAMs) are the major component of the tumor microenvironment (TME), where they sustain tumor progression and or-tumor immunity. Due to their plasticity, macrophages can exhibit anti- or pro-tumor functions through the expression of different gene sets leading to distinct macrophage phenotypes: M1-like or pro-inflammatory and M2-like or anti-inflammatory. NF-κB transcription factors are central regulators of TAMs in cancers, where they often drive macrophage polarization toward an M2-like phenotype. Therefore, the NF-κB pathway is an attractive therapeutic target for cancer immunotherapy in a wide range of human tumors. Hence, targeting NF-κB pathway in the myeloid compartment is a potential clinical strategy to overcome microenvironment-induced immunosuppression and increase anti-tumor immunity. In this review, we discuss the role of NF-κB as a key driver of macrophage functions in tumors as well as the principal strategies to overcome tumor immunosuppression by targeting the NF-κB pathway.
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