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Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer

Local hypoxia is a common feature of many solid tumors and may lead to unsatisfactory chemotherapy outcomes. Anaerobic bacteria that have an affinity to hypoxic areas can be used to achieve targeted drug delivery in tumor tissues. In this study, we developed a biocompatible bacteria/nanoparticles bi...

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Autores principales: Xiao, Susu, Shi, Huan, Zhang, Yan, Fan, Yu, Wang, Li, Xiang, Li, Liu, Yanlin, Zhao, Ling, Fu, Shaozhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976953/
https://www.ncbi.nlm.nih.gov/pubmed/35366890
http://dx.doi.org/10.1186/s12951-022-01373-1
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author Xiao, Susu
Shi, Huan
Zhang, Yan
Fan, Yu
Wang, Li
Xiang, Li
Liu, Yanlin
Zhao, Ling
Fu, Shaozhi
author_facet Xiao, Susu
Shi, Huan
Zhang, Yan
Fan, Yu
Wang, Li
Xiang, Li
Liu, Yanlin
Zhao, Ling
Fu, Shaozhi
author_sort Xiao, Susu
collection PubMed
description Local hypoxia is a common feature of many solid tumors and may lead to unsatisfactory chemotherapy outcomes. Anaerobic bacteria that have an affinity to hypoxic areas can be used to achieve targeted drug delivery in tumor tissues. In this study, we developed a biocompatible bacteria/nanoparticles biohybrid (Bif@DOX-NPs) platform that employs the anaerobic Bifidobacterium infantis (Bif) to deliver adriamycin-loaded bovine serum albumin nanoparticles (DOX-NPs) into breast tumors. The Bif@DOX-NPs retained the targeting ability of B. infantis to hypoxic regions, as well as the cytotoxicity of DOX. The biohybrids were able to actively colonize the hypoxic tumors and significantly increased drug accumulation at the tumor site. The DOX concentration in the tumor masses colonized by Bif@DOX-NPs was 4 times higher than that in the free DOX-treated tumors, which significantly prolonged the median survival of the tumor-bearing mice to 69 days and reduced the toxic side-effects of DOX. Thus, anaerobic bacteria-based biohybrids are a highly promising tool for the targeted treatment of solid tumors with inaccessible hypoxic regions. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01373-1.
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spelling pubmed-89769532022-04-04 Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer Xiao, Susu Shi, Huan Zhang, Yan Fan, Yu Wang, Li Xiang, Li Liu, Yanlin Zhao, Ling Fu, Shaozhi J Nanobiotechnology Research Local hypoxia is a common feature of many solid tumors and may lead to unsatisfactory chemotherapy outcomes. Anaerobic bacteria that have an affinity to hypoxic areas can be used to achieve targeted drug delivery in tumor tissues. In this study, we developed a biocompatible bacteria/nanoparticles biohybrid (Bif@DOX-NPs) platform that employs the anaerobic Bifidobacterium infantis (Bif) to deliver adriamycin-loaded bovine serum albumin nanoparticles (DOX-NPs) into breast tumors. The Bif@DOX-NPs retained the targeting ability of B. infantis to hypoxic regions, as well as the cytotoxicity of DOX. The biohybrids were able to actively colonize the hypoxic tumors and significantly increased drug accumulation at the tumor site. The DOX concentration in the tumor masses colonized by Bif@DOX-NPs was 4 times higher than that in the free DOX-treated tumors, which significantly prolonged the median survival of the tumor-bearing mice to 69 days and reduced the toxic side-effects of DOX. Thus, anaerobic bacteria-based biohybrids are a highly promising tool for the targeted treatment of solid tumors with inaccessible hypoxic regions. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01373-1. BioMed Central 2022-04-02 /pmc/articles/PMC8976953/ /pubmed/35366890 http://dx.doi.org/10.1186/s12951-022-01373-1 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
Xiao, Susu
Shi, Huan
Zhang, Yan
Fan, Yu
Wang, Li
Xiang, Li
Liu, Yanlin
Zhao, Ling
Fu, Shaozhi
Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer
title Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer
title_full Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer
title_fullStr Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer
title_full_unstemmed Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer
title_short Bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer
title_sort bacteria-driven hypoxia targeting delivery of chemotherapeutic drug proving outcome of breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976953/
https://www.ncbi.nlm.nih.gov/pubmed/35366890
http://dx.doi.org/10.1186/s12951-022-01373-1
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