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A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer
BACKGROUND: As an endocytic nanosicle involved in intercellular communication, an exosome can efficiently deliver drugs from one cell to another and deliver therapeutic short interfering RNA (siRNA) to target cells. This is conducive to gene therapy for cancers. In this study, an exosome was used as...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161323/ https://www.ncbi.nlm.nih.gov/pubmed/35545838 http://dx.doi.org/10.1111/1759-7714.14445 |
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author | Lin, Xianbin Lin, Liangan Wu, Jingyang Jiang, Wentan Wu, Jiayun Yang, Jianshen Chen, Chun |
author_facet | Lin, Xianbin Lin, Liangan Wu, Jingyang Jiang, Wentan Wu, Jiayun Yang, Jianshen Chen, Chun |
author_sort | Lin, Xianbin |
collection | PubMed |
description | BACKGROUND: As an endocytic nanosicle involved in intercellular communication, an exosome can efficiently deliver drugs from one cell to another and deliver therapeutic short interfering RNA (siRNA) to target cells. This is conducive to gene therapy for cancers. In this study, an exosome was used as the siRNA‐loaded substrate to prepare a targeted siRNA‐loaded PD‐L1 exosome and evaluate its function against lung cancer. METHODS: The optimal preparation process and binding ratio of the targeted nanovesicle/siRNA complex was determined by detecting the particle size, potential, and other physical parameters in combination with cell binding and uptake capacity of exosome complexes. The biological cell behavior of targeted exosome nanosicles was evaluated through cytotoxicity, apoptosis, and the cell uptake capacity. RESULTS: A targeted exosome nanovesicle capable of loading siRNA and characterized with low toxicity, high loading rate, and the ability to be used for targeted tumor cell gene therapy was constructed. CONCLUSION: The PD‐L1 targeting exosome can be used as an efficient siRNA delivery carrier, which is an efficient and safe nanocarrier for tumor targeted gene therapy. |
format | Online Article Text |
id | pubmed-9161323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-91613232022-06-04 A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer Lin, Xianbin Lin, Liangan Wu, Jingyang Jiang, Wentan Wu, Jiayun Yang, Jianshen Chen, Chun Thorac Cancer Original Articles BACKGROUND: As an endocytic nanosicle involved in intercellular communication, an exosome can efficiently deliver drugs from one cell to another and deliver therapeutic short interfering RNA (siRNA) to target cells. This is conducive to gene therapy for cancers. In this study, an exosome was used as the siRNA‐loaded substrate to prepare a targeted siRNA‐loaded PD‐L1 exosome and evaluate its function against lung cancer. METHODS: The optimal preparation process and binding ratio of the targeted nanovesicle/siRNA complex was determined by detecting the particle size, potential, and other physical parameters in combination with cell binding and uptake capacity of exosome complexes. The biological cell behavior of targeted exosome nanosicles was evaluated through cytotoxicity, apoptosis, and the cell uptake capacity. RESULTS: A targeted exosome nanovesicle capable of loading siRNA and characterized with low toxicity, high loading rate, and the ability to be used for targeted tumor cell gene therapy was constructed. CONCLUSION: The PD‐L1 targeting exosome can be used as an efficient siRNA delivery carrier, which is an efficient and safe nanocarrier for tumor targeted gene therapy. John Wiley & Sons Australia, Ltd 2022-05-11 2022-06 /pmc/articles/PMC9161323/ /pubmed/35545838 http://dx.doi.org/10.1111/1759-7714.14445 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Lin, Xianbin Lin, Liangan Wu, Jingyang Jiang, Wentan Wu, Jiayun Yang, Jianshen Chen, Chun A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer |
title | A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer |
title_full | A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer |
title_fullStr | A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer |
title_full_unstemmed | A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer |
title_short | A targeted siRNA‐loaded PDL1‐exosome and functional evaluation against lung cancer |
title_sort | targeted sirna‐loaded pdl1‐exosome and functional evaluation against lung cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161323/ https://www.ncbi.nlm.nih.gov/pubmed/35545838 http://dx.doi.org/10.1111/1759-7714.14445 |
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