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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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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] |
format | Online Article Text |
id | pubmed-8240398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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