肿瘤微环境
免疫系统
癌症研究
肿瘤进展
免疫疗法
肿瘤相关巨噬细胞
巨噬细胞极化
转移
巨噬细胞
肺癌
癌症免疫疗法
表型
癌症
生物
血管生成
肿瘤发生
免疫学
医学
体外
病理
内科学
基因
生物化学
作者
Yinxue Zhou,Dunqiang Ren,Huanhuan Bi,Bingqian Yi,Cai Zhang,Hongmei Wang,Jiaxing Sun
出处
期刊:PubMed
[National Institutes of Health]
日期:2024-03-20
卷期号:27 (3): 231-240
被引量:6
标识
DOI:10.3779/j.issn.1009-3419.2024.102.13
摘要
Tumor-associated macrophage (TAM) play a crucial role in the immune microenvironment of lung cancer. Through changes in their phenotype and phagocytic functions, TAM contribute to the initiation and progression of lung cancer. By promoting the formation of an immune-suppressive microenvironment and accelerating the growth of abnormal tumor vasculature, TAM facilitate the invasion and metastasis of lung cancer. Macrophages can polarize into different subtypes with distinct functions and characteristics in response to various stimuli, categorized as anti-tumor M1 and pro-tumor M2 types. In tumor tissues, TAM typically polarize into the alternatively activated M2 phenotype, exhibiting inhibitory effects on tumor immunity. This article reviews the role of anti-angiogenic drugs in modulating TAM phenotypes, highlighting their potential to reprogram M2-type TAM into an anti-tumor M1 phenotype. Additionally, the functional alterations of TAM play a significant role in anti-angiogenic therapy and immunotherapy strategies. In summary, the regulation of TAM polarization and function opens up new avenues for lung cancer treatment and may serve as a novel target for modulating the immune microenvironment of tumors. .
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