MicroRNAs in tumor immunity: functional regulation in tumor-associated macrophages

被引:34
作者
Chen, Chong [1 ,2 ,3 ]
Liu, Jia-ming [1 ,2 ,3 ]
Luo, Yun-ping [1 ,2 ,3 ]
机构
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Dept Immunol, Beijing 100005, Peoples R China
[2] Peking Union Med Coll, Sch Basic Med, Beijing 100005, Peoples R China
[3] Chinese Acad Med Sci, Collaborat Innovat Ctr Biotherapy, Inst Basic Med Sci, Beijing 100005, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNA; Tumor microenvironment; Tumor-associated macrophage; Functional polarization; R730; 2; ANTI-HEPATOCELLULAR CARCINOMA; STEM-CELLS; CANCER-CELLS; COLORECTAL-CANCER; POLARIZATION; ACTIVATION; PROMOTES; MIR-146A; DIFFERENTIATION; EXPRESSION;
D O I
10.1631/jzus.B1900452
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor-associated macrophages (TAMs) are the most abundant immune cells in the tumor microenvironment (TME) and are critical for cancer initiation and progression. MicroRNAs (miRNAs) could notably influence the phenotype of TAMs through various targets and signal pathways during cancer progression due to their post-transcriptional regulation. In this review, we discuss mainly the regulatory function of miRNAs on macrophage differentiation, functional polarization, and cellular crosstalk. Firstly, during the generation process, miRNAs take part in the differentiation from myeloid cells to mature macrophages, and this maturation process directly influences their recruitment into the TME, attracted by tumor cells. Secondly, macrophages in the TME can be either tumor-promoting or tumor-suppressing, depending on their functional polarization. Large numbers of miRNAs can influence the polarization of macrophages, which is crucial for tumor progression, including tumor cell invasion, intravasation, extravasation, and premetastatic site formation. Thirdly, crosstalk between tumor cells and macrophages is essential for TME formation and tumor progression, and miRNAs can be the mediator of communication in different forms, especially when encapsulated in microvesicles or exosomes. We also assess the potential value of certain macrophage-related miRNAs (MRMs) as diagnostic and prognostic markers, and discuss the possible development of MRM-based therapies.
引用
收藏
页码:12 / 28
页数:17
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