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Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer
BACKGROUND: Cancer cell membrane-camouflaged nanotechnology for metal complex can enhance its biocompatibility and extend the effective circulation time in body. The ruthenium polypyridyl complex (RuPOP) has extensive antitumor activity, but it still has disadvantages such as poor biocompatibility,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446690/ https://www.ncbi.nlm.nih.gov/pubmed/36064356 http://dx.doi.org/10.1186/s12951-022-01593-5 |
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author | Li, Xiaoying Yu, Yanzi Chen, Qi Lin, Jiabao Zhu, Xueqiong Liu, Xiaoting He, Lizhen Chen, Tianfeng He, Weiling |
author_facet | Li, Xiaoying Yu, Yanzi Chen, Qi Lin, Jiabao Zhu, Xueqiong Liu, Xiaoting He, Lizhen Chen, Tianfeng He, Weiling |
author_sort | Li, Xiaoying |
collection | PubMed |
description | BACKGROUND: Cancer cell membrane-camouflaged nanotechnology for metal complex can enhance its biocompatibility and extend the effective circulation time in body. The ruthenium polypyridyl complex (RuPOP) has extensive antitumor activity, but it still has disadvantages such as poor biocompatibility, lack of targeting, and being easily metabolized by the organism. Cancer cell membranes retain a large number of surface antigens and tumor adhesion molecules CD47, which can be used to camouflage the metal complex and give it tumor homing ability and high biocompatibility. RESULTS: Therefore, this study provides an electrostatic adsorption method, which uses the electrostatic interaction of positive and negative charges between RuPOP and cell membranes to construct a cancer cell membrane-camouflaged nano-platform (RuPOP@CM). Interestingly, RuPOP@CM maintains the expression of surface antigens and tumor adhesion molecules, which can inhibit the phagocytosis of macrophage, reduce the clearance rate of RuPOP, and increase effective circulation time, thus enhancing the accumulation in tumor sites. Besides, RuPOP@CM can enhance the activity of cellular immune response and promote the production of inflammatory cytokines including TNF-α, IL-12 and IL-6, which is of great significance in treatment of tumor. On the other hand, RuPOP@MCM can produce intracellular ROS overproduction, thereby accelerating the apoptosis and cell cycle arrest of tumor cells to play an excellent antitumor effect in vitro and in vivo. CONCLUSION: In brief, engineering cancer cell membrane-camouflaged metal complex is a potential strategy to improve its biocompatibility, biological safety and antitumor effects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01593-5. |
format | Online Article Text |
id | pubmed-9446690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94466902022-09-07 Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer Li, Xiaoying Yu, Yanzi Chen, Qi Lin, Jiabao Zhu, Xueqiong Liu, Xiaoting He, Lizhen Chen, Tianfeng He, Weiling J Nanobiotechnology Research BACKGROUND: Cancer cell membrane-camouflaged nanotechnology for metal complex can enhance its biocompatibility and extend the effective circulation time in body. The ruthenium polypyridyl complex (RuPOP) has extensive antitumor activity, but it still has disadvantages such as poor biocompatibility, lack of targeting, and being easily metabolized by the organism. Cancer cell membranes retain a large number of surface antigens and tumor adhesion molecules CD47, which can be used to camouflage the metal complex and give it tumor homing ability and high biocompatibility. RESULTS: Therefore, this study provides an electrostatic adsorption method, which uses the electrostatic interaction of positive and negative charges between RuPOP and cell membranes to construct a cancer cell membrane-camouflaged nano-platform (RuPOP@CM). Interestingly, RuPOP@CM maintains the expression of surface antigens and tumor adhesion molecules, which can inhibit the phagocytosis of macrophage, reduce the clearance rate of RuPOP, and increase effective circulation time, thus enhancing the accumulation in tumor sites. Besides, RuPOP@CM can enhance the activity of cellular immune response and promote the production of inflammatory cytokines including TNF-α, IL-12 and IL-6, which is of great significance in treatment of tumor. On the other hand, RuPOP@MCM can produce intracellular ROS overproduction, thereby accelerating the apoptosis and cell cycle arrest of tumor cells to play an excellent antitumor effect in vitro and in vivo. CONCLUSION: In brief, engineering cancer cell membrane-camouflaged metal complex is a potential strategy to improve its biocompatibility, biological safety and antitumor effects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01593-5. BioMed Central 2022-09-05 /pmc/articles/PMC9446690/ /pubmed/36064356 http://dx.doi.org/10.1186/s12951-022-01593-5 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 | Research Li, Xiaoying Yu, Yanzi Chen, Qi Lin, Jiabao Zhu, Xueqiong Liu, Xiaoting He, Lizhen Chen, Tianfeng He, Weiling Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer |
title | Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer |
title_full | Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer |
title_fullStr | Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer |
title_full_unstemmed | Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer |
title_short | Engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer |
title_sort | engineering cancer cell membrane-camouflaged metal complex for efficient targeting therapy of breast cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446690/ https://www.ncbi.nlm.nih.gov/pubmed/36064356 http://dx.doi.org/10.1186/s12951-022-01593-5 |
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