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Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma

Melanoma, the most aggressive skin cancer that originated from genetic mutations in the melanocytes, is still a troublesome medical problem under the current therapeutic approaches, which include surgical resection, chemotherapy, photodynamic therapy, immunotherapy, biochemotherapy and targeted ther...

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Autores principales: Hou, Chongchao, Wu, Qiang, Xu, Lizhou, Cui, Rongwei, Ou, Rongying, Li, Danyang, Xu, Yunsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714302/
https://www.ncbi.nlm.nih.gov/pubmed/36466338
http://dx.doi.org/10.3389/fbioe.2022.1054324
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author Hou, Chongchao
Wu, Qiang
Xu, Lizhou
Cui, Rongwei
Ou, Rongying
Li, Danyang
Xu, Yunsheng
author_facet Hou, Chongchao
Wu, Qiang
Xu, Lizhou
Cui, Rongwei
Ou, Rongying
Li, Danyang
Xu, Yunsheng
author_sort Hou, Chongchao
collection PubMed
description Melanoma, the most aggressive skin cancer that originated from genetic mutations in the melanocytes, is still a troublesome medical problem under the current therapeutic approaches, which include surgical resection, chemotherapy, photodynamic therapy, immunotherapy, biochemotherapy and targeted therapy. Nanotechnology has significantly contributed to the development of cancer treatment in the past few years, among which extracellular vesicles (EVs) are nanosized lipid bilayer vesicles secreted from almost all cells that play essential roles in many physiological and pathological processes. In terms of melanoma therapy, the unique physicochemical properties of EVs make them promising nanocarriers for drug transportation compared to other synthetic nanocarriers. Moreover, EVs can be further engineered to maximize their drug delivery potential. Herein, in this minireview, we gave a brief overview of EV-based drug delivery strategies for melanoma therapy, in which different therapeutics delivered via EVs were summarized. We also highlighted the current progress of the EV-based delivery platform for melanoma therapy in clinical trials. The obstacles to applying exosomes in clinical practice toward further translation of EVs melanoma therapy were also discussed at the end. In summary, EVs offer promising prospects for melanoma therapy, whilst the ways for unlocking EVs’ full potential in melanoma therapies should be further investigated by solving relevant issues which hamper EVs-based melanoma therapy translation in the future.
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spelling pubmed-97143022022-12-02 Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma Hou, Chongchao Wu, Qiang Xu, Lizhou Cui, Rongwei Ou, Rongying Li, Danyang Xu, Yunsheng Front Bioeng Biotechnol Bioengineering and Biotechnology Melanoma, the most aggressive skin cancer that originated from genetic mutations in the melanocytes, is still a troublesome medical problem under the current therapeutic approaches, which include surgical resection, chemotherapy, photodynamic therapy, immunotherapy, biochemotherapy and targeted therapy. Nanotechnology has significantly contributed to the development of cancer treatment in the past few years, among which extracellular vesicles (EVs) are nanosized lipid bilayer vesicles secreted from almost all cells that play essential roles in many physiological and pathological processes. In terms of melanoma therapy, the unique physicochemical properties of EVs make them promising nanocarriers for drug transportation compared to other synthetic nanocarriers. Moreover, EVs can be further engineered to maximize their drug delivery potential. Herein, in this minireview, we gave a brief overview of EV-based drug delivery strategies for melanoma therapy, in which different therapeutics delivered via EVs were summarized. We also highlighted the current progress of the EV-based delivery platform for melanoma therapy in clinical trials. The obstacles to applying exosomes in clinical practice toward further translation of EVs melanoma therapy were also discussed at the end. In summary, EVs offer promising prospects for melanoma therapy, whilst the ways for unlocking EVs’ full potential in melanoma therapies should be further investigated by solving relevant issues which hamper EVs-based melanoma therapy translation in the future. Frontiers Media S.A. 2022-11-17 /pmc/articles/PMC9714302/ /pubmed/36466338 http://dx.doi.org/10.3389/fbioe.2022.1054324 Text en Copyright © 2022 Hou, Wu, Xu, Cui, Ou, Li and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Hou, Chongchao
Wu, Qiang
Xu, Lizhou
Cui, Rongwei
Ou, Rongying
Li, Danyang
Xu, Yunsheng
Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma
title Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma
title_full Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma
title_fullStr Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma
title_full_unstemmed Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma
title_short Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma
title_sort exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714302/
https://www.ncbi.nlm.nih.gov/pubmed/36466338
http://dx.doi.org/10.3389/fbioe.2022.1054324
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