Exosome-Mediated Therapeutic Strategies for Management of Solid and Hematological Malignancies

被引:15
作者
Allegra, Alessandro [1 ]
Petrarca, Claudia [2 ,3 ]
Di Gioacchino, Mario [2 ,4 ]
Casciaro, Marco [5 ]
Musolino, Caterina [1 ]
Gangemi, Sebastiano [5 ]
机构
[1] Univ Messina, Dept Human Pathol Adulthood & Childhood Gaetano B, Div Hematol, I-98125 Messina, Italy
[2] Univ G dAnnunzio, Ctr Adv Studies & Technol, I-66100 Chieti, Italy
[3] Univ G dAnnunzio, Dept Med & Aging Sci, I-66100 Chieti, Italy
[4] Inst Clin Immunotherapy & Adv Biol Treatments, I-65100 Pescara, Italy
[5] Univ Messina, Sch Allergy & Clin Immunol, Dept Clin & Expt Med, Unit Allergy & Clin Immunol, I-98125 Messina, Italy
关键词
extracellular vesicles; exosome; cancer; hematological malignancy; cell communication; chemoresistance; microRNA; drug delivery; immune response; CELL-DERIVED EXOSOMES; MESENCHYMAL STROMAL CELLS; COLON-CANCER CELLS; INHIBIT IN-VITRO; BREAST-CANCER; DELIVERY-SYSTEMS; OVARIAN-CANCER; EXTRACELLULAR VESICLES; LEUKEMIA-CELLS; STEM-CELLS;
D O I
10.3390/cells11071128
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Exosomes are small membrane vesicles of endocytic origin containing cytokines, RNAs, growth factors, proteins, lipids, and metabolites. They have been identified as fundamental intercellular communication controllers in several diseases and an enormous volume of data confirmed that exosomes could either sustain or inhibit tumor onset and diffusion in diverse solid and hematological malignancies by paracrine signaling. Thus, exosomes might constitute a promising cell-free tumor treatment alternative. This review focuses on the effects of exosomes in the treatment of tumors, by discussing the most recent and promising data from in vitro and experimental in vivo studies and the few existing clinical trials. Exosomes are extremely promising as transporters of drugs, antagomir, genes, and other therapeutic substances that can be integrated into their core via different procedures. Moreover, exosomes can augment or inhibit non-coding RNAs, change the metabolism of cancer cells, and modify the function of immunologic effectors thus modifying the tumor microenvironment transforming it from pro-tumor to antitumor milieu. Here, we report the development of currently realized exosome modifiers that offer indications for the forthcoming elaboration of other more effective methods capable of enhancing the activity of the exosomes.
引用
收藏
页数:33
相关论文
共 224 条
[91]   Development of exosome-encapsulated paclitaxel to overcome MDR in cancer cells [J].
Kim, Myung Soo ;
Haney, Matthew J. ;
Zhao, Yuling ;
Mahajan, Vivek ;
Deygen, Irina ;
Klyachko, Natalia L. ;
Inskoe, Eli ;
Piroyan, Aleksandr ;
Sokolsky, Marina ;
Okolie, Onyi ;
Hingtgen, Shawn D. ;
Kabanov, Alexander V. ;
Batrakova, Elena V. .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2016, 12 (03) :655-664
[92]   Adipose-Derived Mesenchymal Stem Cell Exosomes Suppress Hepatocellular Carcinoma Growth in a Rat Model: Apparent Diffusion Coefficient, Natural Killer T-Cell Responses, and Histopathological Features [J].
Ko, Sheung-Fat ;
Yip, Hon-Kan ;
Zhen, Yen-Yi ;
Lee, Chen-Chang ;
Lee, Chia-Chang ;
Huang, Chung-Cheng ;
Ng, Shu-Hang ;
Lin, Jui-Wei .
STEM CELLS INTERNATIONAL, 2015, 2015
[93]   Exploring the potential of engineered exosomes as delivery systems for tumor-suppressor microRNA replacement therapy in ovarian cancer [J].
Kobayashi, Masaki ;
Sawada, Kenjiro ;
Miyamoto, Mayuko ;
Shimizu, Aasa ;
Yamamoto, Misa ;
Kinose, Yasuto ;
Nakamura, Koji ;
Kawano, Mahiru ;
Kodama, Michiko ;
Hashimoto, Kae ;
Kimura, Tadashi .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2020, 527 (01) :153-161
[94]   Populational equilibrium through exosome-mediated Wnt signaling in tumor progression of diffuse large B-cell lymphoma [J].
Koch, Raphael ;
Demant, Martin ;
Aung, Thiha ;
Diering, Nina ;
Cicholas, Anna ;
Chapuy, Bjoern ;
Wenzel, Dirk ;
Lahmann, Marlen ;
Guentsch, Annemarie ;
Kiecke, Christina ;
Becker, Sabrina ;
Hupfeld, Timo ;
Venkataramani, Vivek ;
Ziepert, Marita ;
Opitz, Lennart ;
Klapper, Wolfram ;
Truemper, Lorenz ;
Wulf, Gerald G. .
BLOOD, 2014, 123 (14) :2189-2198
[95]   MSC-derived exosomes: a novel tool to treat therapy-refractory graft-versus-host disease [J].
Kordelas, L. ;
Rebmann, V. ;
Ludwig, A-K ;
Radtke, S. ;
Ruesing, J. ;
Doeppner, T. R. ;
Epple, M. ;
Horn, P. A. ;
Beelen, D. W. ;
Giebel, B. .
LEUKEMIA, 2014, 28 (04) :970-973
[96]   Extracellular Vesicles as Natural Nanosized Delivery Systems for Small-Molecule Drugs and Genetic Material: Steps towards the Future Nanomedicines [J].
Kotmakci, Mustafa ;
Cetintas, Vildan B. .
JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, 2015, 18 (03) :396-413
[97]   Circular RNA Expression Profile of Pancreatic Ductal Adenocarcinoma Revealed by Microarray [J].
Li, Haimin ;
Hao, Xiaokun ;
Wang, Huimin ;
Liu, Zhengcai ;
He, Yong ;
Pu, Meng ;
Zhang, Hongtao ;
Yu, Hengchao ;
Duan, Juanli ;
Qu, Shibin .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2016, 40 (06) :1334-1344
[98]   Exosomes derived from siRNA against GRP78 modified bone-marrow-derived mesenchymal stem cells suppress Sorafenib resistance in hepatocellular carcinoma [J].
Li, Hongdan ;
Yang, Cheng ;
Shi, Yijie ;
Zhao, Liang .
JOURNAL OF NANOBIOTECHNOLOGY, 2018, 16
[99]   A Multifunctional Polymeric Nanotheranostic System Delivers Doxorubicin and Imaging Agents across the Blood-Brain Barrier Targeting Brain Metastases of Breast Cancer [J].
Li, Jason ;
Cai, Ping ;
Shalviri, Alireza ;
Henderson, Jeffrey T. ;
He, Chunsheng ;
Foltz, Warren D. ;
Prasad, Preethy ;
Brodersen, Peter M. ;
Chen, Yonghong ;
DaCosta, Ralph ;
Rauth, Andrew Michael ;
Wu, Xiao Yu .
ACS NANO, 2014, 8 (10) :9925-9940
[100]   Rab27B enhances drug resistance in hepatocellular carcinoma by promoting exosome-mediated drug efflux [J].
Li, Rui ;
Dong, Chengyong ;
Jiang, Keqiu ;
Sun, Rui ;
Zhou, Yang ;
Yin, Zeli ;
Lv, Jiaxin ;
Zhang, Junlin ;
Wang, Qi ;
Wang, Liming .
CARCINOGENESIS, 2020, 41 (11) :1583-1591