MicroRNA networks regulate the differentiation, expansion and suppression function of myeloid-derived suppressor cells in tumor microenvironment

被引:25
|
作者
Su, Yanping [1 ]
Qiu, Ye [2 ]
Qiu, Zhidong [3 ]
Qu, Peng [4 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Dept Histol & Embryol, Tai An, Shandong, Peoples R China
[2] Northeast Normal Univ, Natl Engn Lab Druggable Gene & Prot Screening, Changchun, Jilin, Peoples R China
[3] Changchun Univ Chinese Med, Dept Pharm, Changchun, Jilin, Peoples R China
[4] NCI, NIH, Frederick, MD 21702 USA
来源
JOURNAL OF CANCER | 2019年 / 10卷 / 18期
基金
中国国家自然科学基金;
关键词
MicroRNA; Myeloid-derived suppressor cells; Tumor; CANCER; EXPRESSION; PROMOTES; INFLAMMATION; MIR-21; ACTIVATION; PLASTICITY; MECHANISM; APOPTOSIS; SEPSIS;
D O I
10.7150/jca.35205
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Myeloid-derived suppressor cells (MDSCs), one heterogeneous population of immature myeloid cells, have suppressive function on immune response during tumor, inflammation, infection and autoimmune diseases. The molecular mechanism underlying expansion and function of MDSCs is becoming appreciated to manipulate immune response in the diseases. MicroRNA (miRNAs) as one short noncoding RNAs, are involved in regulating cell proliferation, differentiation and maturation. However, it needs to be further studied how miRNAs mediate the development and function of MDSC in association with cancer and other diseases. In the review, we report and discuss recent studies that miRNAs networks regulate the differentiation, expansion and suppression function of MDSCs in tumor microenvironment or other diseases through different signaling pathways. Those studies may provide one novel potential approach for tumor immunotherapy.
引用
收藏
页码:4350 / 4356
页数:7
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