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Which cell death modality wins the contest for photodynamic therapy of cancer?

Photodynamic therapy (PDT) was discovered more than 100 years ago. Since then, many protocols and agents for PDT have been proposed for the treatment of several types of cancer. Traditionally, cell death induced by PDT was categorized into three types: apoptosis, cell death associated with autophagy...

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Autores principales: Mishchenko, Tatiana, Balalaeva, Irina, Gorokhova, Anastasia, Vedunova, Maria, Krysko, Dmitri V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106666/
https://www.ncbi.nlm.nih.gov/pubmed/35562364
http://dx.doi.org/10.1038/s41419-022-04851-4
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author Mishchenko, Tatiana
Balalaeva, Irina
Gorokhova, Anastasia
Vedunova, Maria
Krysko, Dmitri V.
author_facet Mishchenko, Tatiana
Balalaeva, Irina
Gorokhova, Anastasia
Vedunova, Maria
Krysko, Dmitri V.
author_sort Mishchenko, Tatiana
collection PubMed
description Photodynamic therapy (PDT) was discovered more than 100 years ago. Since then, many protocols and agents for PDT have been proposed for the treatment of several types of cancer. Traditionally, cell death induced by PDT was categorized into three types: apoptosis, cell death associated with autophagy, and necrosis. However, with the discovery of several other regulated cell death modalities in recent years, it has become clear that this is a rather simple understanding of the mechanisms of action of PDT. New observations revealed that cancer cells exposed to PDT can pass through various non-conventional cell death pathways, such as paraptosis, parthanatos, mitotic catastrophe, pyroptosis, necroptosis, and ferroptosis. Nowadays, immunogenic cell death (ICD) has become one of the most promising ways to eradicate tumor cells by activation of the T-cell adaptive immune response and induction of long-term immunological memory. ICD can be triggered by many anti-cancer treatment methods, including PDT. In this review, we critically discuss recent findings on the non-conventional cell death mechanisms triggered by PDT. Next, we emphasize the role and contribution of ICD in these PDT-induced non-conventional cell death modalities. Finally, we discuss the obstacles and propose several areas of research that will help to overcome these challenges and lead to the development of highly effective anti-cancer therapy based on PDT.
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spelling pubmed-91066662022-05-15 Which cell death modality wins the contest for photodynamic therapy of cancer? Mishchenko, Tatiana Balalaeva, Irina Gorokhova, Anastasia Vedunova, Maria Krysko, Dmitri V. Cell Death Dis Review Article Photodynamic therapy (PDT) was discovered more than 100 years ago. Since then, many protocols and agents for PDT have been proposed for the treatment of several types of cancer. Traditionally, cell death induced by PDT was categorized into three types: apoptosis, cell death associated with autophagy, and necrosis. However, with the discovery of several other regulated cell death modalities in recent years, it has become clear that this is a rather simple understanding of the mechanisms of action of PDT. New observations revealed that cancer cells exposed to PDT can pass through various non-conventional cell death pathways, such as paraptosis, parthanatos, mitotic catastrophe, pyroptosis, necroptosis, and ferroptosis. Nowadays, immunogenic cell death (ICD) has become one of the most promising ways to eradicate tumor cells by activation of the T-cell adaptive immune response and induction of long-term immunological memory. ICD can be triggered by many anti-cancer treatment methods, including PDT. In this review, we critically discuss recent findings on the non-conventional cell death mechanisms triggered by PDT. Next, we emphasize the role and contribution of ICD in these PDT-induced non-conventional cell death modalities. Finally, we discuss the obstacles and propose several areas of research that will help to overcome these challenges and lead to the development of highly effective anti-cancer therapy based on PDT. Nature Publishing Group UK 2022-05-13 /pmc/articles/PMC9106666/ /pubmed/35562364 http://dx.doi.org/10.1038/s41419-022-04851-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Mishchenko, Tatiana
Balalaeva, Irina
Gorokhova, Anastasia
Vedunova, Maria
Krysko, Dmitri V.
Which cell death modality wins the contest for photodynamic therapy of cancer?
title Which cell death modality wins the contest for photodynamic therapy of cancer?
title_full Which cell death modality wins the contest for photodynamic therapy of cancer?
title_fullStr Which cell death modality wins the contest for photodynamic therapy of cancer?
title_full_unstemmed Which cell death modality wins the contest for photodynamic therapy of cancer?
title_short Which cell death modality wins the contest for photodynamic therapy of cancer?
title_sort which cell death modality wins the contest for photodynamic therapy of cancer?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106666/
https://www.ncbi.nlm.nih.gov/pubmed/35562364
http://dx.doi.org/10.1038/s41419-022-04851-4
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