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Chemodynamic nanomaterials for cancer theranostics

It is of utmost urgency to achieve effective and safe anticancer treatment with the increasing mortality rate of cancer. Novel anticancer drugs and strategies need to be designed for enhanced therapeutic efficacy. Fenton- and Fenton-like reaction-based chemodynamic therapy (CDT) are new strategies t...

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Autores principales: Xin, Jingqi, Deng, Caiting, Aras, Omer, Zhou, Mengjiao, Wu, Chunsheng, An, Feifei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240398/
https://www.ncbi.nlm.nih.gov/pubmed/34183023
http://dx.doi.org/10.1186/s12951-021-00936-y
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author Xin, Jingqi
Deng, Caiting
Aras, Omer
Zhou, Mengjiao
Wu, Chunsheng
An, Feifei
author_facet Xin, Jingqi
Deng, Caiting
Aras, Omer
Zhou, Mengjiao
Wu, Chunsheng
An, Feifei
author_sort Xin, Jingqi
collection PubMed
description It is of utmost urgency to achieve effective and safe anticancer treatment with the increasing mortality rate of cancer. Novel anticancer drugs and strategies need to be designed for enhanced therapeutic efficacy. Fenton- and Fenton-like reaction-based chemodynamic therapy (CDT) are new strategies to enhance anticancer efficacy due to their capacity to generate reactive oxygen species (ROS) and oxygen (O(2)). On the one hand, the generated ROS can damage the cancer cells directly. On the other hand, the generated O(2) can relieve the hypoxic condition in the tumor microenvironment (TME) which hinders efficient photodynamic therapy, radiotherapy, etc. Therefore, CDT can be used together with many other therapeutic strategies for synergistically enhanced combination therapy. The antitumor applications of Fenton- and Fenton-like reaction-based nanomaterials will be discussed in this review, including: (iþ) producing abundant ROS in-situ to kill cancer cells directly, (ii) enhancing therapeutic efficiency indirectly by Fenton reaction-mediated combination therapy, (iii) diagnosis and monitoring of cancer therapy. These strategies exhibit the potential of CDT-based nanomaterials for efficient cancer therapy. [Image: see text]
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spelling pubmed-82403982021-06-30 Chemodynamic nanomaterials for cancer theranostics Xin, Jingqi Deng, Caiting Aras, Omer Zhou, Mengjiao Wu, Chunsheng An, Feifei J Nanobiotechnology Review It is of utmost urgency to achieve effective and safe anticancer treatment with the increasing mortality rate of cancer. Novel anticancer drugs and strategies need to be designed for enhanced therapeutic efficacy. Fenton- and Fenton-like reaction-based chemodynamic therapy (CDT) are new strategies to enhance anticancer efficacy due to their capacity to generate reactive oxygen species (ROS) and oxygen (O(2)). On the one hand, the generated ROS can damage the cancer cells directly. On the other hand, the generated O(2) can relieve the hypoxic condition in the tumor microenvironment (TME) which hinders efficient photodynamic therapy, radiotherapy, etc. Therefore, CDT can be used together with many other therapeutic strategies for synergistically enhanced combination therapy. The antitumor applications of Fenton- and Fenton-like reaction-based nanomaterials will be discussed in this review, including: (iþ) producing abundant ROS in-situ to kill cancer cells directly, (ii) enhancing therapeutic efficiency indirectly by Fenton reaction-mediated combination therapy, (iii) diagnosis and monitoring of cancer therapy. These strategies exhibit the potential of CDT-based nanomaterials for efficient cancer therapy. [Image: see text] BioMed Central 2021-06-28 /pmc/articles/PMC8240398/ /pubmed/34183023 http://dx.doi.org/10.1186/s12951-021-00936-y Text en © The Author(s) 2021 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 Review
Xin, Jingqi
Deng, Caiting
Aras, Omer
Zhou, Mengjiao
Wu, Chunsheng
An, Feifei
Chemodynamic nanomaterials for cancer theranostics
title Chemodynamic nanomaterials for cancer theranostics
title_full Chemodynamic nanomaterials for cancer theranostics
title_fullStr Chemodynamic nanomaterials for cancer theranostics
title_full_unstemmed Chemodynamic nanomaterials for cancer theranostics
title_short Chemodynamic nanomaterials for cancer theranostics
title_sort chemodynamic nanomaterials for cancer theranostics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240398/
https://www.ncbi.nlm.nih.gov/pubmed/34183023
http://dx.doi.org/10.1186/s12951-021-00936-y
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