MiRNAs: dynamic regulators of immune cell functions in inflammation and cancer

被引:97
作者
Hirschberger, Simon [1 ,2 ]
Hinske, Ludwig Christian [1 ]
Kreth, Simone [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Anesthesiol, Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Walter Brendel Ctr Expt Med, Munich, Germany
关键词
Immuno-miRs; Immune cell function; MicroRNA-containing exosomes; Tumor immune escape; EPITHELIAL OVARIAN-CANCER; DENDRITIC CELLS; SUPPRESSOR-CELLS; GENE-EXPRESSION; T-CELLS; MIR-17-SIMILAR-TO-92; FAMILY; MICRORNA BIOGENESIS; MAMMALIAN MICRORNAS; TARGET RECOGNITION; NONCODING RNAS;
D O I
10.1016/j.canlet.2018.05.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs), small noncoding RNA molecules, have emerged as important regulators of almost all cellular processes. By binding to specific sequence motifs within the 3 '-untranslated region of their target mRNAs, they induce either mRNA degradation or translational repression. In the human immune system, potent miRNAs and miRNA-clusters have been discovered, that exert pivotal roles in the regulation of gene expression. By targeting cellular signaling hubs, these so-called immuno-miRs have fundamental regulative impact on both innate and adaptive immune cells in health and disease. Importantly, they also act as mediators of tumor immune escape. Secreted by cancer cells and consecutively taken up by immune cells, immuno-miRs are capable to influence immune functions towards a blunted anti-tumor response, thus shaping a permissive tumor environment. This review provides an overview of immuno-miRs and their functional impact on individual immune cell entities. Further, implications of immuno-miRs in the amelioration of tumor surveillance are discussed.
引用
收藏
页码:11 / 21
页数:11
相关论文
共 154 条
[1]   MicroRNAs Transfer from Human Macrophages to Hepato-Carcinoma Cells and Inhibit Proliferation [J].
Aucher, Anne ;
Rudnicka, Dominika ;
Davis, Daniel M. .
JOURNAL OF IMMUNOLOGY, 2013, 191 (12) :6250-6260
[2]   The impact of microRNAs on protein output [J].
Baek, Daehyun ;
Villen, Judit ;
Shin, Chanseok ;
Camargo, Fernando D. ;
Gygi, Steven P. ;
Bartel, David P. .
NATURE, 2008, 455 (7209) :64-U38
[3]  
Bandara Kanchana Veronika, 2017, Microrna, V6, P80, DOI 10.2174/2211536606666170313114821
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[5]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[6]   NLRP3 Inflammasome Activity Is Negatively Controlled by miR-223 [J].
Bauernfeind, Franz ;
Rieger, Anna ;
Schildberg, Frank A. ;
Knolle, Percy A. ;
Schmid-Burgk, Jonathan L. ;
Hornung, Veit .
JOURNAL OF IMMUNOLOGY, 2012, 189 (08) :4175-4181
[7]   The microRNA cluster miR-17∼92 promotes TFH cell differentiation and represses subset-inappropriate gene expression [J].
Baumjohann, Dirk ;
Kageyama, Robin ;
Clingan, Jonathan M. ;
Morar, Malika M. ;
Patel, Sana ;
de Kouchkovsky, Dimitri ;
Bannard, Oliver ;
Bluestone, Jeffrey A. ;
Matloubian, Mehrdad ;
Ansel, K. Mark ;
Jeker, Lukas T. .
NATURE IMMUNOLOGY, 2013, 14 (08) :840-+
[8]   A regulatory interplay between miR-27a and Runx1 during megakaryopoiesis [J].
Ben-Ami, Oren ;
Pencovich, Niv ;
Lotem, Joseph ;
Levanon, Ditsa ;
Groner, Yoram .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (01) :238-243
[9]   RETRACTED: miR-181a Induces Macrophage Polarized to M2 Phenotype and Promotes M2 Macrophage-mediated Tumor Cell Metastasis by Targeting KLF6 and C/EBPα (Retracted article. See vol. 28, pg. 792, 2022) [J].
Bi, Jia ;
Zeng, Xianxin ;
Zhao, Lin ;
Wei, Qian ;
Yu, Lifeng ;
Wang, Xinnan ;
Yu, Zhaojin ;
Cao, Yaming ;
Shan, Fengping ;
Wei, Minjie .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2016, 5 :e368
[10]   Alternative Polyadenylation Directs Tissue-Specific miRNA Targeting in Caenorhabditis elegans Somatic Tissues [J].
Blazie, Stephen M. ;
Geissel, Heather C. ;
Wilky, Henry ;
Joshi, Rajan ;
Newbern, Jason ;
Mangone, Marco .
GENETICS, 2017, 206 (02) :757-774