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Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy

Photodynamic therapy (PDT) is performed using a photosensitizer and light of specific wavelength in the presence of oxygen to generate singlet oxygen and reactive oxygen species(ROS) in the cancer cells. The accumulated photosensitizers in target sites induce ROS generation upon light activation, th...

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Detalles Bibliográficos
Autores principales: Hwang, Hee Sook, Shin, Heejun, Han, Jieun, Na, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323106/
https://www.ncbi.nlm.nih.gov/pubmed/30680248
http://dx.doi.org/10.1007/s40005-017-0377-x
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author Hwang, Hee Sook
Shin, Heejun
Han, Jieun
Na, Kun
author_facet Hwang, Hee Sook
Shin, Heejun
Han, Jieun
Na, Kun
author_sort Hwang, Hee Sook
collection PubMed
description Photodynamic therapy (PDT) is performed using a photosensitizer and light of specific wavelength in the presence of oxygen to generate singlet oxygen and reactive oxygen species(ROS) in the cancer cells. The accumulated photosensitizers in target sites induce ROS generation upon light activation, then the generated cytotoxic reactive oxygen species lead to tumor cell death via apoptosis or necrosis, and damages the target sites which results tumor destruction. As a consequence, the PDT-mediated cell death is associated with anti-tumor immune response. In this paper, the effects of PDT and immune response on tumors are reviewed. Activation of an immune response regarding the innate and adaptive immune response, interaction with immune cells and tumor cells that associated with antitumor efficacy of PDT are also discussed.
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spelling pubmed-63231062019-01-22 Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy Hwang, Hee Sook Shin, Heejun Han, Jieun Na, Kun J Pharm Investig Review Photodynamic therapy (PDT) is performed using a photosensitizer and light of specific wavelength in the presence of oxygen to generate singlet oxygen and reactive oxygen species(ROS) in the cancer cells. The accumulated photosensitizers in target sites induce ROS generation upon light activation, then the generated cytotoxic reactive oxygen species lead to tumor cell death via apoptosis or necrosis, and damages the target sites which results tumor destruction. As a consequence, the PDT-mediated cell death is associated with anti-tumor immune response. In this paper, the effects of PDT and immune response on tumors are reviewed. Activation of an immune response regarding the innate and adaptive immune response, interaction with immune cells and tumor cells that associated with antitumor efficacy of PDT are also discussed. Springer Singapore 2018-11-01 2018 /pmc/articles/PMC6323106/ /pubmed/30680248 http://dx.doi.org/10.1007/s40005-017-0377-x Text en © The Author(s) 2017, corrected publication October 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, 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.
spellingShingle Review
Hwang, Hee Sook
Shin, Heejun
Han, Jieun
Na, Kun
Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy
title Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy
title_full Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy
title_fullStr Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy
title_full_unstemmed Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy
title_short Combination of photodynamic therapy (PDT) and anti-tumor immunity in cancer therapy
title_sort combination of photodynamic therapy (pdt) and anti-tumor immunity in cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323106/
https://www.ncbi.nlm.nih.gov/pubmed/30680248
http://dx.doi.org/10.1007/s40005-017-0377-x
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