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Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy

BACKGROUND: Radiotherapy is a commonly used tool in clinical practice to treat solid tumors. However, due to the unique microenvironment inside the tumor, such as high levels of GSH, overexpressed H(2)O(2) and hypoxia, these factors can seriously affect the effectiveness of radiotherapy. RESULTS: Th...

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Autores principales: Pi, Fen, Deng, Xuanru, Xue, Qian, Zheng, Lan, Liu, Hongxing, Yang, Fang, Chen, Tianfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018832/
https://www.ncbi.nlm.nih.gov/pubmed/36922836
http://dx.doi.org/10.1186/s12951-023-01850-1
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author Pi, Fen
Deng, Xuanru
Xue, Qian
Zheng, Lan
Liu, Hongxing
Yang, Fang
Chen, Tianfeng
author_facet Pi, Fen
Deng, Xuanru
Xue, Qian
Zheng, Lan
Liu, Hongxing
Yang, Fang
Chen, Tianfeng
author_sort Pi, Fen
collection PubMed
description BACKGROUND: Radiotherapy is a commonly used tool in clinical practice to treat solid tumors. However, due to the unique microenvironment inside the tumor, such as high levels of GSH, overexpressed H(2)O(2) and hypoxia, these factors can seriously affect the effectiveness of radiotherapy. RESULTS: Therefore, to further improve the efficiency of radiotherapy, a core–shell nanocomposite CeO(2)–MnO(2) is designed as a novel radiosensitizer that can modulate the tumor microenvironment (TME) and thus improve the efficacy of radiation therapy. CeO(2)–MnO(2) can act as a radiosensitizer to enhance X-ray absorption at the tumor site while triggering the response behavior associated with the tumor microenvironment. According to in vivo and in vitro experiments, the nanoparticles aggravate the killing effect on tumor cells by generating large amounts of ROS and disrupting the redox balance. In this process, the outer layer of MnO(2) reacts with GSH and H(2)O(2) in the tumor microenvironment to generate ROS and release oxygen, thus alleviating the hypoxic condition in the tumor area. Meanwhile, the manganese ions produced by degradation can enhance T1-weighted magnetic resonance imaging (MRI). In addition, CeO(2)–MnO(2), due to its high atomic number oxide CeO(2), releases a large number of electrons under the effect of radiotherapy, which further reacts with intracellular molecules to produce reactive oxygen species and enhances the killing effect on tumor cells, thus having the effect of radiotherapy sensitization. In conclusion, the nanomaterial CeO(2)–MnO(2), as a novel radiosensitizer, greatly improves the efficiency of cancer radiation therapy by improving the lack of oxygen in tumor and responding to the tumor microenvironment, providing an effective strategy for the construction of nanosystem with radiosensitizing function. CONCLUSION: In conclusion, the nanomaterial CeO(2)–MnO(2), as a novel radiosensitizer, greatly improves the efficiency of cancer radiation therapy by improving the lack of oxygen in tumor and responding to the tumor microenvironment, providing an effective strategy for the construction of nanosystems with radiosensitizing function. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01850-1.
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spelling pubmed-100188322023-03-17 Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy Pi, Fen Deng, Xuanru Xue, Qian Zheng, Lan Liu, Hongxing Yang, Fang Chen, Tianfeng J Nanobiotechnology Research BACKGROUND: Radiotherapy is a commonly used tool in clinical practice to treat solid tumors. However, due to the unique microenvironment inside the tumor, such as high levels of GSH, overexpressed H(2)O(2) and hypoxia, these factors can seriously affect the effectiveness of radiotherapy. RESULTS: Therefore, to further improve the efficiency of radiotherapy, a core–shell nanocomposite CeO(2)–MnO(2) is designed as a novel radiosensitizer that can modulate the tumor microenvironment (TME) and thus improve the efficacy of radiation therapy. CeO(2)–MnO(2) can act as a radiosensitizer to enhance X-ray absorption at the tumor site while triggering the response behavior associated with the tumor microenvironment. According to in vivo and in vitro experiments, the nanoparticles aggravate the killing effect on tumor cells by generating large amounts of ROS and disrupting the redox balance. In this process, the outer layer of MnO(2) reacts with GSH and H(2)O(2) in the tumor microenvironment to generate ROS and release oxygen, thus alleviating the hypoxic condition in the tumor area. Meanwhile, the manganese ions produced by degradation can enhance T1-weighted magnetic resonance imaging (MRI). In addition, CeO(2)–MnO(2), due to its high atomic number oxide CeO(2), releases a large number of electrons under the effect of radiotherapy, which further reacts with intracellular molecules to produce reactive oxygen species and enhances the killing effect on tumor cells, thus having the effect of radiotherapy sensitization. In conclusion, the nanomaterial CeO(2)–MnO(2), as a novel radiosensitizer, greatly improves the efficiency of cancer radiation therapy by improving the lack of oxygen in tumor and responding to the tumor microenvironment, providing an effective strategy for the construction of nanosystem with radiosensitizing function. CONCLUSION: In conclusion, the nanomaterial CeO(2)–MnO(2), as a novel radiosensitizer, greatly improves the efficiency of cancer radiation therapy by improving the lack of oxygen in tumor and responding to the tumor microenvironment, providing an effective strategy for the construction of nanosystems with radiosensitizing function. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01850-1. BioMed Central 2023-03-15 /pmc/articles/PMC10018832/ /pubmed/36922836 http://dx.doi.org/10.1186/s12951-023-01850-1 Text en © The Author(s) 2023 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
Pi, Fen
Deng, Xuanru
Xue, Qian
Zheng, Lan
Liu, Hongxing
Yang, Fang
Chen, Tianfeng
Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy
title Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy
title_full Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy
title_fullStr Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy
title_full_unstemmed Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy
title_short Alleviating the hypoxic tumor microenvironment with MnO(2)-coated CeO(2) nanoplatform for magnetic resonance imaging guided radiotherapy
title_sort alleviating the hypoxic tumor microenvironment with mno(2)-coated ceo(2) nanoplatform for magnetic resonance imaging guided radiotherapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018832/
https://www.ncbi.nlm.nih.gov/pubmed/36922836
http://dx.doi.org/10.1186/s12951-023-01850-1
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