Exosomal microRNAs-mediated intercellular communication and exosome-based cancer treatment

被引:34
作者
Shi, Zhao-Yu [1 ]
Yang, Xiao-Xia [1 ]
Malichewe, ChristinaYallen [1 ]
Li, Ying-Shuang [1 ]
Guo, Xiu-Li [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Dept Pharmacol, Key Lab Chem Biol,Minist Educ, Jinan 250012, Peoples R China
关键词
Exosomes; MicroRNAs; Intercellular communication; MESENCHYMAL TRANSITION EMT; BREAST-CANCER; CISPLATIN RESISTANCE; POTENTIAL BIOMARKER; CELL-MIGRATION; GROWTH-FACTOR; DELIVERY; BIOGENESIS; MIR-21; SECRETION;
D O I
10.1016/j.ijbiomac.2020.04.228
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
Exosomes are extracellular vesicles with a diameter of about 30 to 100 nm, which play a crucial role in intercel-lular communication. Compared with normal cells, the release rate of tumor-derived exosomes (TDEs) signifi-cantly increased, and exosomal contents, especially microRNAs (miRNAs), greatly changed. TDEs contribute to the proliferation, metastasis and resistance of tumor cells, regulate immune response and tumor autophagy, and mediate tumor-stroma communication. In addition, exosomes may be involved in tumor complications. In view of the role of exosomes in intercellular communication, exosomes have been developed as tumor bio-markers, therapeutic targets, and drug delivery systems for tumor diagnosis, prognosis and treatment. Despite the many advantages of exosomes, there are many challenges in exosomal development and application, such as incomprehensive understanding of biological functions, safety and specificity for therapeutic use. This article reviews the biogenesis of TDEs and focuses on the role of exosomal miRNAs in intercellular communication and exosome-based treatment for cancer. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:530 / 541
页数:12
相关论文
共 141 条
[1]   Investigation of miR-21, miR-141, and miR-221 in blood circulation of patients with prostate cancer [J].
Agaoglu, Fulya Yaman ;
Kovancilar, Muge ;
Dizdar, Yavuz ;
Darendeliler, Emin ;
Holdenrieder, Stefan ;
Dalay, Nejat ;
Gezer, Ugur .
TUMOR BIOLOGY, 2011, 32 (03) :583-588
[2]   Up-regulated exosomal miRNA-140-3p in CML patients with musculoskeletal pain associated with discontinuation of tyrosine kinase inhibitors [J].
Asano, Michiyo ;
Umezu, Tomohiro ;
Katagiri, Seiichiro ;
Kobayashi, Chiaki ;
Tauchi, Tetsuzo ;
Gotoh, Moritaka ;
Ando, Keiko ;
Okabe, Seiichi ;
Ohyashiki, Junko H. ;
Ohyashiki, Kazuma .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2017, 105 (04) :419-422
[3]   Exosomes in cancer: Use them or target them? [J].
Bastos, Nuno ;
Ruivo, Carolina F. ;
da Silva, Soraia ;
Melo, Sonia A. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2018, 78 :13-21
[4]  
Batra Jaspreet Singh, 2014, J Biomark, V2014, P321680, DOI 10.1155/2014/321680
[5]   Hypoxic tumor-derived microvesicles negatively regulate NK cell function by a mechanism involving TGF- and miR23a transfer [J].
Berchem, Guy ;
Noman, Muhammad Zaeem ;
Bosseler, Manon ;
Paggetti, Jerome ;
Baconnais, Sonia ;
Le Cam, Eric ;
Nanbakhsh, Arash ;
Moussay, Etienne ;
Mami-Chouaib, Fathia ;
Janji, Bassam ;
Chouaib, Salem .
ONCOIMMUNOLOGY, 2016, 5 (04)
[6]   Dendritic cell-derived exosomes as maintenance immunotherapy after first line chemotherapy in NSCLC [J].
Besse, Benjamin ;
Charrier, Melinda ;
Lapierre, Valerie ;
Dansin, Eric ;
Lantz, Olivier ;
Planchard, David ;
Le Chevalier, Thierry ;
Livartoski, Alain ;
Barlesik, Fabrice ;
Laplanche, Agnes ;
Ploix, Stephanie ;
Vimond, Nadege ;
Peguillet, Isabelle ;
Thery, Clotilde ;
Lacroix, Ludovic ;
Zoernig, Inka ;
Dhodapkar, Kavita ;
Dhodapkar, Madhav ;
Viaud, Sophie ;
Soria, Jean-Charles ;
Reiners, Katrin S. ;
von Strandmann, Elke Pogge ;
Vely, Frederic ;
Rusakiewicz, Sylvie ;
Eggermont, Alexander ;
Pitt, Jonathan M. ;
Zitvogel, Laurence ;
Chaput, Nathalie .
ONCOIMMUNOLOGY, 2016, 5 (04)
[7]   Transfer of miRNA in Macrophage-Derived Exosomes Induces Drug Resistance in Pancreatic Adenocarcinoma [J].
Binenbaum, Yoav ;
Fridman, Eran ;
Yaari, Zvi ;
Milman, Neta ;
Schroeder, Avi ;
Ben David, Gil ;
Shlomi, Tomer ;
Gil, Ziv .
CANCER RESEARCH, 2018, 78 (18) :5287-5299
[8]   Exosomes in bodily fluids are a highly stable resource of disease biomarkers [J].
Boukouris, Stephanie ;
Mathivanan, Suresh .
PROTEOMICS CLINICAL APPLICATIONS, 2015, 9 (3-4) :358-367
[9]   Exosomal miR-21 regulates the TETs/PTENp1/PTEN pathway to promote hepatocellular carcinoma growth [J].
Cao, Liang-qi ;
Yang, Xue-wei ;
Chen, Yu-bin ;
Zhang, Da-wei ;
Jiang, Xiao-Feng ;
Xue, Ping .
MOLECULAR CANCER, 2019, 18 (01)
[10]   MiR-23a regulates TGF-β-induced epithelial-mesenchymal transition by targeting E-cadherin in lung cancer cells [J].
Cao, Mengru ;
Seike, Masahiro ;
Soeno, Chie ;
Mizutani, Hideaki ;
Kitamura, Kazuhiro ;
Minegishi, Yuji ;
Noro, Rintaro ;
Yoshimura, Akinobu ;
Cai, Li ;
Gemma, Akihiko .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2012, 41 (03) :869-875