Cancer-derived exosomic microRNAs shape the immune system within the tumor microenvironment: State of the art

被引:59
作者
Fanini, Francesca [1 ]
Fabbri, Muller [2 ,3 ,4 ]
机构
[1] Ist Sci Romagnolo Studio & Cura Tumori IRST Srl I, Unit Gene Therapy, I-47014 Meldola, FC, Italy
[2] Univ Southern Calif, Childrens Ctr Canc & Blood Dis, Dept Pediat, Los Angeles, CA 90027 USA
[3] Univ Southern Calif, Childrens Ctr Canc & Blood Dis, Dept Mol Microbiol & Immunol, Norris Comprehens Canc Ctr,Keck Sch Med, Los Angeles, CA 90027 USA
[4] Childrens Hosp Los Angeles, Saban Res Inst, Los Angeles, CA 90027 USA
关键词
Tumor-derived exosomes; microRNAs; Cancer; Immune system; Microenvironment; REGULATORY T-CELLS; TOLL-LIKE RECEPTORS; DENDRITIC CELLS; MESSENGER-RNAS; MACROPHAGE; EXPRESSION; DIFFERENTIATION; MECHANISM; MICROVESICLES; INFILTRATION;
D O I
10.1016/j.semcdb.2016.12.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In recent years there has been an increasing interest of the scientific community on exosome research, with particular emphasis on the mechanisms by which tumor-derived exosomes can promote tumor growth. Particularly, exosome-mediated immune-escape is under deep investigation and still represents a quite controversial issue. Tumor-derived exosomes are carriers of information able to reprogram functions of immune target cells, influencing their development, maturation, and antitumor activities. They deliver proteins similar to those of the parent cancer cells, but also genetic messages like genomic DNA, mRNA, and microRNAs (miRNAs) that ultimately share the so called "tumor microenvironment" in a pro-tumoral fashion. The content of tumor-derived exosomes could be implicated in several signaling pathways operating in the tumor microenvironment, providing a further modality of dys-regulation of antitumor immunity. The aim of this review is to provide a state-of-the-art highlight of to the most recent discoveries in the field of interaction between tumor-derived exosomic miRNAs and the cells of immune system. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:23 / 28
页数:6
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