Functions of Cancer-Derived Extracellular Vesicles in Immunosuppression

被引:0
作者
Liliana Czernek
Markus Düchler
机构
[1] Polish Academy of Sciences,Department of Bioorganic Chemistry, Centre of Molecular and Macromolecular Studies
来源
Archivum Immunologiae et Therapiae Experimentalis | 2017年 / 65卷
关键词
Exosomes; Extracellular vesicles; Cancer immunosuppression; Suppressor cells; Immune escape;
D O I
暂无
中图分类号
学科分类号
摘要
Extracellular vesicles, including exosomes, constitute an important element of intercellular communication by carrying a variety of molecules from producer to target cells. The transport of mRNA and miRNA can directly modulate gene expression in the target cells. The miRNA content in exosomes is characteristic for the cell from which the vesicles were derived enabling the usage of exosomes as biomarkers for the diagnosis various diseases, including cancer. Cancer-derived exosomes support the survival and progression of tumors in many ways and also contribute to the neutralization of the anti-cancer immune response. Exosomes participate in all known mechanisms by which cancer evades the immune system. They influence the differentiation and activation of immune suppressor cells, they modulate antigen presentation, and are able to induce T-cell apoptosis. Although cancer-derived exosomes mainly suppress the immune system and facilitate tumor progression, they are also important sources of tumor antigens with potential clinical application in stimulating immune responses. This review summarizes how exosomes assist cancer to escape immune recognition and to acquire control over the immune system.
引用
收藏
页码:311 / 323
页数:12
相关论文
共 431 条
  • [1] Abusamra AJ(2005)Tumor exosomes expressing Fas ligand mediate CD8 Blood Cells Mol Dis 35 169-173
  • [2] Zhong Z(2015) T-cell apoptosis Nat Commun 6 7321-624
  • [3] Zheng X(2008)Exosome-delivered microRNAs modulate the inflammatory response to endotoxin Nat Cell Biol 10 619-3799
  • [4] Alexander M(2009)Intercellular transfer of the oncogenic receptor EGFRvIII by microvesicles derived from tumour cells Proc Natl Acad Sci USA 106 3794-2136
  • [5] Hu R(2004)Endothelial expression of autocrine VEGF upon the uptake of tumor-derived microvesicles containing oncogenic EGFR J Immunol 172 2126-1316
  • [6] Runtsch MC(2002)Exosomes as potent cell-free peptide-based vaccine. I. Dendritic cell-derived exosomes transfer functional MHC class I/peptide complexes to dendritic cells J Exp Med 195 1303-312
  • [7] Al-Nedawi K(2013)Induction of lymphocyte apoptosis by tumor cell secretion of FasL-bearing microvesicles Stem Cell Res 10 301-685
  • [8] Meehan B(2016)Mesenchymal stem cell-derived exosomes increase ATP levels, decrease oxidative stress and activate PI3K/Akt pathway to enhance myocardial viability and prevent adverse remodeling after myocardial ischemia/reperfusion injury Sci Rep 6 35376-529
  • [9] Micallef J(2012)Massive release of extracellular vesicles from cancer cells after photodynamic treatment or chemotherapy Nat Cell Biol 14 677-3241
  • [10] Al-Nedawi K(2016)Syndecan-syntenin-ALIX regulates the biogenesis of exosomes J Transl Med 14 36-2679