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Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action

Platinum-based anticancer drugs are a class of widely used agents in clinical cancer treatment. However, their efficacy was greatly limited by their severe side effects and the arising drug resistance. The selective activation of inert platinum-based drugs in the tumor site by light irradiation is a...

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Autores principales: Dai, Ziwen, Wang, Zhigang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664195/
https://www.ncbi.nlm.nih.gov/pubmed/33171980
http://dx.doi.org/10.3390/molecules25215167
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author Dai, Ziwen
Wang, Zhigang
author_facet Dai, Ziwen
Wang, Zhigang
author_sort Dai, Ziwen
collection PubMed
description Platinum-based anticancer drugs are a class of widely used agents in clinical cancer treatment. However, their efficacy was greatly limited by their severe side effects and the arising drug resistance. The selective activation of inert platinum-based drugs in the tumor site by light irradiation is able to reduce side effects, and the novel mechanism of action of photoactivatable platinum drugs might also conquer the resistance. In this review, the recent advances in the design of photoactivatable platinum-based drugs were summarized. The complexes are classified according to their mode of action, including photoreduction, photo-uncaging, and photodissociation. The rationale of drug design, dark stability, photoactivation process, cytotoxicity, and mechanism of action of typical photoactivatable platinum drugs were reviewed. Finally, the challenges and opportunities for designing more potent photoactivatable platinum drugs were discussed.
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spelling pubmed-76641952020-11-14 Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action Dai, Ziwen Wang, Zhigang Molecules Review Platinum-based anticancer drugs are a class of widely used agents in clinical cancer treatment. However, their efficacy was greatly limited by their severe side effects and the arising drug resistance. The selective activation of inert platinum-based drugs in the tumor site by light irradiation is able to reduce side effects, and the novel mechanism of action of photoactivatable platinum drugs might also conquer the resistance. In this review, the recent advances in the design of photoactivatable platinum-based drugs were summarized. The complexes are classified according to their mode of action, including photoreduction, photo-uncaging, and photodissociation. The rationale of drug design, dark stability, photoactivation process, cytotoxicity, and mechanism of action of typical photoactivatable platinum drugs were reviewed. Finally, the challenges and opportunities for designing more potent photoactivatable platinum drugs were discussed. MDPI 2020-11-06 /pmc/articles/PMC7664195/ /pubmed/33171980 http://dx.doi.org/10.3390/molecules25215167 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dai, Ziwen
Wang, Zhigang
Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action
title Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action
title_full Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action
title_fullStr Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action
title_full_unstemmed Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action
title_short Photoactivatable Platinum-Based Anticancer Drugs: Mode of Photoactivation and Mechanism of Action
title_sort photoactivatable platinum-based anticancer drugs: mode of photoactivation and mechanism of action
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664195/
https://www.ncbi.nlm.nih.gov/pubmed/33171980
http://dx.doi.org/10.3390/molecules25215167
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