Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells

Detalhes bibliográficos
Autor(a) principal: de Melo Gomes, Laura Calazans
Data de Publicação: 2023
Outros Autores: de Oliveira Cunha, Amanda Branquinho, Peixoto, Luiz Felipe Fernandes, Zanon, Renata Graciele, Botelho, Françoise Vasconcelos, Silva, Marcelo José Barbosa, Pinto-Fochi, Maria Etelvina, Góes, Rejane Maira [UNESP], de Paoli, Flávia, Ribeiro, Daniele Lisboa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s43630-023-00382-9
http://hdl.handle.net/11449/249716
Resumo: Prostate cancer is the most common cancer in American men, aside from skin cancer. As an alternative cancer treatment, photodynamic laser therapy (PDT) can be used to induce cell death. We evaluated the PDT effect, using methylene blue as a photosensitizer, in human prostate tumor cells (PC3). PC3 were subjected to four different conditions: DMEM (control); laser treatment (L—660 nm, 100 mW, 100 J.cm−2); methylene blue treatment (MB—25 μM, 30 min), and MB treatment followed by low-level red laser irradiation (MB-PDT). Groups were evaluated after 24 h. MB-PDT treatment reduced cell viability and migration. However, because MB-PDT did not significantly increase the levels of active caspase-3 and BCL-2, apoptosis was not the primary mode of cell death. MB-PDT, on the other hand, increased the acid compartment by 100% and the LC3 immunofluorescence (an autophagy marker) by 254%. Active MLKL level, a necroptosis marker, was higher in PC3 cells after MB-PDT treatment. Furthermore, MB-PDT resulted in oxidative stress due to a decrease in total antioxidant potential, catalase levels, and increased lipid peroxidation. According to these findings, MB-PDT therapy is effective at inducing oxidative stress and reducing PC3 cell viability. In such therapy, necroptosis is also an important mechanism of cell death triggered by autophagy. Graphical Abstract: [Figure not available: see fulltext.]
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spelling Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cellsCell deathMethylene bluePhotodynamic therapyProstate cancerProstate cancer is the most common cancer in American men, aside from skin cancer. As an alternative cancer treatment, photodynamic laser therapy (PDT) can be used to induce cell death. We evaluated the PDT effect, using methylene blue as a photosensitizer, in human prostate tumor cells (PC3). PC3 were subjected to four different conditions: DMEM (control); laser treatment (L—660 nm, 100 mW, 100 J.cm−2); methylene blue treatment (MB—25 μM, 30 min), and MB treatment followed by low-level red laser irradiation (MB-PDT). Groups were evaluated after 24 h. MB-PDT treatment reduced cell viability and migration. However, because MB-PDT did not significantly increase the levels of active caspase-3 and BCL-2, apoptosis was not the primary mode of cell death. MB-PDT, on the other hand, increased the acid compartment by 100% and the LC3 immunofluorescence (an autophagy marker) by 254%. Active MLKL level, a necroptosis marker, was higher in PC3 cells after MB-PDT treatment. Furthermore, MB-PDT resulted in oxidative stress due to a decrease in total antioxidant potential, catalase levels, and increased lipid peroxidation. According to these findings, MB-PDT therapy is effective at inducing oxidative stress and reducing PC3 cell viability. In such therapy, necroptosis is also an important mechanism of cell death triggered by autophagy. Graphical Abstract: [Figure not available: see fulltext.]Department of Cell Biology Histology and Embryology. Institute of Biomedical Sciences-ICBIM Federal University of Uberlândia-UFU, Minas GeraisDepartment of Anatomy. Institute of Biomedical Sciences-ICBIM Federal University of Uberlândia-UFU, Minas GeraisInstitute of Biotechnology-IBTEC Federal University of Uberlândia-UFU, Minas GeraisDepartment of Immunology Institute of Biomedical Sciences-ICBIM Federal University of Uberlândia-UFU, Minas GeraisFaculdade de Medicina União das Faculdades Dos Grandes Lagos São José Do Rio Preto-São PauloDepartment of Biology Institute of Biosciences Humanities and Exact Sciences São Paulo State University-UNESPDepartment of Morphology Institute of Biological Sciences Federal University of Juiz de Fora-UFJF, Minas GeraisDepartment of Biology Institute of Biosciences Humanities and Exact Sciences São Paulo State University-UNESPUniversidade Federal de Uberlândia (UFU)São José Do Rio Preto-São PauloUniversidade Estadual Paulista (UNESP)Federal University of Juiz de Fora-UFJFde Melo Gomes, Laura Calazansde Oliveira Cunha, Amanda BranquinhoPeixoto, Luiz Felipe FernandesZanon, Renata GracieleBotelho, Françoise VasconcelosSilva, Marcelo José BarbosaPinto-Fochi, Maria EtelvinaGóes, Rejane Maira [UNESP]de Paoli, FláviaRibeiro, Daniele Lisboa2023-07-29T16:07:18Z2023-07-29T16:07:18Z2023-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s43630-023-00382-9Photochemical and Photobiological Sciences.1474-90921474-905Xhttp://hdl.handle.net/11449/24971610.1007/s43630-023-00382-92-s2.0-85149204525Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPhotochemical and Photobiological Sciencesinfo:eu-repo/semantics/openAccess2023-07-29T16:07:18Zoai:repositorio.unesp.br:11449/249716Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-07-29T16:07:18Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
title Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
spellingShingle Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
de Melo Gomes, Laura Calazans
Cell death
Methylene blue
Photodynamic therapy
Prostate cancer
title_short Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
title_full Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
title_fullStr Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
title_full_unstemmed Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
title_sort Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells
author de Melo Gomes, Laura Calazans
author_facet de Melo Gomes, Laura Calazans
de Oliveira Cunha, Amanda Branquinho
Peixoto, Luiz Felipe Fernandes
Zanon, Renata Graciele
Botelho, Françoise Vasconcelos
Silva, Marcelo José Barbosa
Pinto-Fochi, Maria Etelvina
Góes, Rejane Maira [UNESP]
de Paoli, Flávia
Ribeiro, Daniele Lisboa
author_role author
author2 de Oliveira Cunha, Amanda Branquinho
Peixoto, Luiz Felipe Fernandes
Zanon, Renata Graciele
Botelho, Françoise Vasconcelos
Silva, Marcelo José Barbosa
Pinto-Fochi, Maria Etelvina
Góes, Rejane Maira [UNESP]
de Paoli, Flávia
Ribeiro, Daniele Lisboa
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Uberlândia (UFU)
São José Do Rio Preto-São Paulo
Universidade Estadual Paulista (UNESP)
Federal University of Juiz de Fora-UFJF
dc.contributor.author.fl_str_mv de Melo Gomes, Laura Calazans
de Oliveira Cunha, Amanda Branquinho
Peixoto, Luiz Felipe Fernandes
Zanon, Renata Graciele
Botelho, Françoise Vasconcelos
Silva, Marcelo José Barbosa
Pinto-Fochi, Maria Etelvina
Góes, Rejane Maira [UNESP]
de Paoli, Flávia
Ribeiro, Daniele Lisboa
dc.subject.por.fl_str_mv Cell death
Methylene blue
Photodynamic therapy
Prostate cancer
topic Cell death
Methylene blue
Photodynamic therapy
Prostate cancer
description Prostate cancer is the most common cancer in American men, aside from skin cancer. As an alternative cancer treatment, photodynamic laser therapy (PDT) can be used to induce cell death. We evaluated the PDT effect, using methylene blue as a photosensitizer, in human prostate tumor cells (PC3). PC3 were subjected to four different conditions: DMEM (control); laser treatment (L—660 nm, 100 mW, 100 J.cm−2); methylene blue treatment (MB—25 μM, 30 min), and MB treatment followed by low-level red laser irradiation (MB-PDT). Groups were evaluated after 24 h. MB-PDT treatment reduced cell viability and migration. However, because MB-PDT did not significantly increase the levels of active caspase-3 and BCL-2, apoptosis was not the primary mode of cell death. MB-PDT, on the other hand, increased the acid compartment by 100% and the LC3 immunofluorescence (an autophagy marker) by 254%. Active MLKL level, a necroptosis marker, was higher in PC3 cells after MB-PDT treatment. Furthermore, MB-PDT resulted in oxidative stress due to a decrease in total antioxidant potential, catalase levels, and increased lipid peroxidation. According to these findings, MB-PDT therapy is effective at inducing oxidative stress and reducing PC3 cell viability. In such therapy, necroptosis is also an important mechanism of cell death triggered by autophagy. Graphical Abstract: [Figure not available: see fulltext.]
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T16:07:18Z
2023-07-29T16:07:18Z
2023-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s43630-023-00382-9
Photochemical and Photobiological Sciences.
1474-9092
1474-905X
http://hdl.handle.net/11449/249716
10.1007/s43630-023-00382-9
2-s2.0-85149204525
url http://dx.doi.org/10.1007/s43630-023-00382-9
http://hdl.handle.net/11449/249716
identifier_str_mv Photochemical and Photobiological Sciences.
1474-9092
1474-905X
10.1007/s43630-023-00382-9
2-s2.0-85149204525
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Photochemical and Photobiological Sciences
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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