微泡
外体
肿瘤微环境
癌症研究
肿瘤进展
小RNA
巨噬细胞极化
免疫系统
转移
血管生成
生物
肿瘤相关巨噬细胞
巨噬细胞
免疫学
癌症
体外
基因
生物化学
遗传学
作者
Xintong Zhou,Qi Liu,Xiaomin Wang,Xiaoyu Yao,Baogang Zhang,Jibiao Wu,Changgang Sun
出处
期刊:Cancer Letters
[Elsevier]
日期:2022-10-25
卷期号:552: 215975-215975
被引量:16
标识
DOI:10.1016/j.canlet.2022.215975
摘要
As a biological carrier, exosomes participate in the communication between various kinds of cells, and can mediate the interactive ‘dialogue’ between tumor cells and tumor-associated macrophages (TAMs). TAMs are the most abundant cell population in the tumor stroma and are an important part of the tumor immune microenvironment. Various stimulating factors in the tumor microenvironment influence the polarization of TAMs into multiple phenotypes, such as M1 and M2. It plays a dual role in tumor immunity by both promoting and inhibiting tumor growth. Exosome-encapsulated non-coding RNAs (ncRNAs) participate in the interactive ‘dialogue’ between exosome-mediated TAMs and tumor cells. Tumor-derived exosomal ncRNAs can promote macrophage polarization, whereas exosomal ncRNAs derived from TAMs can affect tumor proliferation, metastasis, angiogenesis, and chemotherapy resistance. The present review summarizes the dual effects of exosomal ncRNAs on tumor cells and TAMs, and discusses the application of exosomal ncRNAs as a potential diagnostic or prognostic marker and drug delivery system, to provide a new perspective and potential therapeutic drugs on targeting exosomes and macrophages in the treatment of tumors.
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