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Application of engineered extracellular vesicles for targeted tumor therapy

All cells, including prokaryotes and eukaryotes, could release extracellular vesicles (EVs). EVs contain many cellular components, including RNA, and surface proteins, and are essential for maintaining normal intercellular communication and homeostasis of the internal environment. EVs released from...

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Autores principales: Zhang, Fusheng, Guo, Jinshuai, Zhang, Zhenghou, Duan, Meiqi, Wang, Guang, Qian, Yiping, Zhao, Haiying, Yang, Zhi, Jiang, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862579/
https://www.ncbi.nlm.nih.gov/pubmed/35189894
http://dx.doi.org/10.1186/s12929-022-00798-y
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author Zhang, Fusheng
Guo, Jinshuai
Zhang, Zhenghou
Duan, Meiqi
Wang, Guang
Qian, Yiping
Zhao, Haiying
Yang, Zhi
Jiang, Xiaofeng
author_facet Zhang, Fusheng
Guo, Jinshuai
Zhang, Zhenghou
Duan, Meiqi
Wang, Guang
Qian, Yiping
Zhao, Haiying
Yang, Zhi
Jiang, Xiaofeng
author_sort Zhang, Fusheng
collection PubMed
description All cells, including prokaryotes and eukaryotes, could release extracellular vesicles (EVs). EVs contain many cellular components, including RNA, and surface proteins, and are essential for maintaining normal intercellular communication and homeostasis of the internal environment. EVs released from different tissues and cells exhibit excellent properties and functions (e.g., targeting specificity, regulatory ability, physical durability, and immunogenicity), rendering them a potential new option for drug delivery and precision therapy. EVs have been demonstrated to transport antitumor drugs for tumor therapy; additionally, EVs' contents and surface substance can be altered to improve their therapeutic efficacy in the clinic by boosting targeting potential and drug delivery effectiveness. EVs can regulate immune system function by affecting the tumor microenvironment, thereby inhibiting tumor progression. Co-delivery systems for EVs can be utilized to further improve the drug delivery efficiency of EVs, including hydrogels and liposomes. In this review, we discuss the isolation technologies of EVs, as well as engineering approaches to their modification. Moreover, we evaluate the therapeutic potential of EVs in tumors, including engineered extracellular vesicles and EVs' co-delivery systems.
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spelling pubmed-88625792022-02-23 Application of engineered extracellular vesicles for targeted tumor therapy Zhang, Fusheng Guo, Jinshuai Zhang, Zhenghou Duan, Meiqi Wang, Guang Qian, Yiping Zhao, Haiying Yang, Zhi Jiang, Xiaofeng J Biomed Sci Review All cells, including prokaryotes and eukaryotes, could release extracellular vesicles (EVs). EVs contain many cellular components, including RNA, and surface proteins, and are essential for maintaining normal intercellular communication and homeostasis of the internal environment. EVs released from different tissues and cells exhibit excellent properties and functions (e.g., targeting specificity, regulatory ability, physical durability, and immunogenicity), rendering them a potential new option for drug delivery and precision therapy. EVs have been demonstrated to transport antitumor drugs for tumor therapy; additionally, EVs' contents and surface substance can be altered to improve their therapeutic efficacy in the clinic by boosting targeting potential and drug delivery effectiveness. EVs can regulate immune system function by affecting the tumor microenvironment, thereby inhibiting tumor progression. Co-delivery systems for EVs can be utilized to further improve the drug delivery efficiency of EVs, including hydrogels and liposomes. In this review, we discuss the isolation technologies of EVs, as well as engineering approaches to their modification. Moreover, we evaluate the therapeutic potential of EVs in tumors, including engineered extracellular vesicles and EVs' co-delivery systems. BioMed Central 2022-02-21 /pmc/articles/PMC8862579/ /pubmed/35189894 http://dx.doi.org/10.1186/s12929-022-00798-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Zhang, Fusheng
Guo, Jinshuai
Zhang, Zhenghou
Duan, Meiqi
Wang, Guang
Qian, Yiping
Zhao, Haiying
Yang, Zhi
Jiang, Xiaofeng
Application of engineered extracellular vesicles for targeted tumor therapy
title Application of engineered extracellular vesicles for targeted tumor therapy
title_full Application of engineered extracellular vesicles for targeted tumor therapy
title_fullStr Application of engineered extracellular vesicles for targeted tumor therapy
title_full_unstemmed Application of engineered extracellular vesicles for targeted tumor therapy
title_short Application of engineered extracellular vesicles for targeted tumor therapy
title_sort application of engineered extracellular vesicles for targeted tumor therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862579/
https://www.ncbi.nlm.nih.gov/pubmed/35189894
http://dx.doi.org/10.1186/s12929-022-00798-y
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