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Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence
Developing a living prosthetic breast to inhibit potential breast cancer recurrence and simultaneously promote breast reconstruction would be a promising strategy for clinical treatment of breast cancer after mastectomy. Here, a living prosthetic breast in the form of injectable gelatin methacryloyl...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487338/ https://www.ncbi.nlm.nih.gov/pubmed/37693055 http://dx.doi.org/10.1002/btm2.10409 |
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author | Xu, Wenting Huang, Yu Yuen, Ho‐Yin Shi, Linli Qian, Haiqing Cui, Lijuan Tang, Mengyu Wang, Jiahui Zhu, Jie Wang, Zhirong Xiao, Long Zhao, Xin Wang, Lihong |
author_facet | Xu, Wenting Huang, Yu Yuen, Ho‐Yin Shi, Linli Qian, Haiqing Cui, Lijuan Tang, Mengyu Wang, Jiahui Zhu, Jie Wang, Zhirong Xiao, Long Zhao, Xin Wang, Lihong |
author_sort | Xu, Wenting |
collection | PubMed |
description | Developing a living prosthetic breast to inhibit potential breast cancer recurrence and simultaneously promote breast reconstruction would be a promising strategy for clinical treatment of breast cancer after mastectomy. Here, a living prosthetic breast in the form of injectable gelatin methacryloyl microspheres is prepared, where they encapsulated zeolitic imidazolate framework (ZIF) nanoparticles loaded with small molecules urolithin C (Uro‐C) and adipose‐derived stem cells (ADSCs). Taking advantage of the acidic tumor microenvironment, the ZIF triggered a pH‐sensitive drug release in situ so that Uro‐C can induce tumor cell apoptosis via reactive oxygen species (ROS) generation. Meanwhile, the ADSCs proliferate in situ to promote tissue regeneration. Using such a design, our data showed that the ADSCs maintained viable and proliferate under the inhibitory effect of Uro‐C in vitro. Through ROS generation, Uro‐C also activated a suppressive tumor microenvironment in mice by both re‐polarizing M2 macrophages to M1 macrophages for elevated inflammatory responses, and increasing the ratio between CD8 and CD4 T cells for tumor recurrence inhibition, significantly promoting new adipose tissue formation. Altogether, our results demonstrate that the prepared living prosthetic breast with bifunctional properties can be a promising candidate in clinic involving tumor treatment and tissue engineering in synergy. |
format | Online Article Text |
id | pubmed-10487338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104873382023-09-09 Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence Xu, Wenting Huang, Yu Yuen, Ho‐Yin Shi, Linli Qian, Haiqing Cui, Lijuan Tang, Mengyu Wang, Jiahui Zhu, Jie Wang, Zhirong Xiao, Long Zhao, Xin Wang, Lihong Bioeng Transl Med Special Issue Articles Developing a living prosthetic breast to inhibit potential breast cancer recurrence and simultaneously promote breast reconstruction would be a promising strategy for clinical treatment of breast cancer after mastectomy. Here, a living prosthetic breast in the form of injectable gelatin methacryloyl microspheres is prepared, where they encapsulated zeolitic imidazolate framework (ZIF) nanoparticles loaded with small molecules urolithin C (Uro‐C) and adipose‐derived stem cells (ADSCs). Taking advantage of the acidic tumor microenvironment, the ZIF triggered a pH‐sensitive drug release in situ so that Uro‐C can induce tumor cell apoptosis via reactive oxygen species (ROS) generation. Meanwhile, the ADSCs proliferate in situ to promote tissue regeneration. Using such a design, our data showed that the ADSCs maintained viable and proliferate under the inhibitory effect of Uro‐C in vitro. Through ROS generation, Uro‐C also activated a suppressive tumor microenvironment in mice by both re‐polarizing M2 macrophages to M1 macrophages for elevated inflammatory responses, and increasing the ratio between CD8 and CD4 T cells for tumor recurrence inhibition, significantly promoting new adipose tissue formation. Altogether, our results demonstrate that the prepared living prosthetic breast with bifunctional properties can be a promising candidate in clinic involving tumor treatment and tissue engineering in synergy. John Wiley & Sons, Inc. 2022-09-20 /pmc/articles/PMC10487338/ /pubmed/37693055 http://dx.doi.org/10.1002/btm2.10409 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. 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 | Special Issue Articles Xu, Wenting Huang, Yu Yuen, Ho‐Yin Shi, Linli Qian, Haiqing Cui, Lijuan Tang, Mengyu Wang, Jiahui Zhu, Jie Wang, Zhirong Xiao, Long Zhao, Xin Wang, Lihong Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence |
title | Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence |
title_full | Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence |
title_fullStr | Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence |
title_full_unstemmed | Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence |
title_short | Living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence |
title_sort | living prosthetic breast for promoting tissue regeneration and inhibiting tumor recurrence |
topic | Special Issue Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487338/ https://www.ncbi.nlm.nih.gov/pubmed/37693055 http://dx.doi.org/10.1002/btm2.10409 |
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