Autophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light

Glioblastoma is one of the most aggressive types of tumors. Although few treatment options are currently available, new modalities are needed to improve prognosis. In this context, photodynamic therapy (PDT) is a promising adjuvant treatment modality. In the present work, hypericin-mediated PDT (hyp...

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Autores principales: Viktoria Pevna, Georges Wagnières, Veronika Huntosova
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:5a7d69b034f141ea91dff5449db815a42021-11-25T16:51:00ZAutophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light10.3390/biomedicines91117032227-9059https://doaj.org/article/5a7d69b034f141ea91dff5449db815a42021-11-01T00:00:00Zhttps://www.mdpi.com/2227-9059/9/11/1703https://doaj.org/toc/2227-9059Glioblastoma is one of the most aggressive types of tumors. Although few treatment options are currently available, new modalities are needed to improve prognosis. In this context, photodynamic therapy (PDT) is a promising adjuvant treatment modality. In the present work, hypericin-mediated PDT (hypericin-PDT, 2 J/cm<sup>2</sup>) of U87 MG cells is combined with (2 min, 15 mW/cm<sup>2</sup> at 808 nm) photobiomodulation (PBM). We observed that PBM stimulates autophagy, which, in combination with PDT, increases the treatment efficacy and leads to apoptosis. Confocal fluorescence microscopy, cytotoxicity assays and Western blot were used to monitor apoptotic and autophagic processes in these cells. Destabilization of lysosomes, mitochondria and the Golgi apparatus led to an increase in lactate dehydrogenase activity, oxidative stress levels, LC3-II, and caspase-3, as well as a decrease of the PKCα and STAT3 protein levels in response to hypericin-PDT subcellular concentration in U87 MG cells. Our results indicate that therapeutic hypericin concentrations can be reduced when PDT is combined with PBM. This will likely allow to reduce the damage induced in surrounding healthy tissues when PBM-hypericin-PDT is used for in vivo tumor treatments.Viktoria PevnaGeorges WagnièresVeronika HuntosovaMDPI AGarticleglioblastoma cellsautophagyphotodynamic therapyphotobiomodulationapoptosismicroscopyBiology (General)QH301-705.5ENBiomedicines, Vol 9, Iss 1703, p 1703 (2021)
institution DOAJ
collection DOAJ
language EN
topic glioblastoma cells
autophagy
photodynamic therapy
photobiomodulation
apoptosis
microscopy
Biology (General)
QH301-705.5
spellingShingle glioblastoma cells
autophagy
photodynamic therapy
photobiomodulation
apoptosis
microscopy
Biology (General)
QH301-705.5
Viktoria Pevna
Georges Wagnières
Veronika Huntosova
Autophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light
description Glioblastoma is one of the most aggressive types of tumors. Although few treatment options are currently available, new modalities are needed to improve prognosis. In this context, photodynamic therapy (PDT) is a promising adjuvant treatment modality. In the present work, hypericin-mediated PDT (hypericin-PDT, 2 J/cm<sup>2</sup>) of U87 MG cells is combined with (2 min, 15 mW/cm<sup>2</sup> at 808 nm) photobiomodulation (PBM). We observed that PBM stimulates autophagy, which, in combination with PDT, increases the treatment efficacy and leads to apoptosis. Confocal fluorescence microscopy, cytotoxicity assays and Western blot were used to monitor apoptotic and autophagic processes in these cells. Destabilization of lysosomes, mitochondria and the Golgi apparatus led to an increase in lactate dehydrogenase activity, oxidative stress levels, LC3-II, and caspase-3, as well as a decrease of the PKCα and STAT3 protein levels in response to hypericin-PDT subcellular concentration in U87 MG cells. Our results indicate that therapeutic hypericin concentrations can be reduced when PDT is combined with PBM. This will likely allow to reduce the damage induced in surrounding healthy tissues when PBM-hypericin-PDT is used for in vivo tumor treatments.
format article
author Viktoria Pevna
Georges Wagnières
Veronika Huntosova
author_facet Viktoria Pevna
Georges Wagnières
Veronika Huntosova
author_sort Viktoria Pevna
title Autophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light
title_short Autophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light
title_full Autophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light
title_fullStr Autophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light
title_full_unstemmed Autophagy and Apoptosis Induced in U87 MG Glioblastoma Cells by Hypericin-Mediated Photodynamic Therapy Can Be Photobiomodulated with 808 nm Light
title_sort autophagy and apoptosis induced in u87 mg glioblastoma cells by hypericin-mediated photodynamic therapy can be photobiomodulated with 808 nm light
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/5a7d69b034f141ea91dff5449db815a4
work_keys_str_mv AT viktoriapevna autophagyandapoptosisinducedinu87mgglioblastomacellsbyhypericinmediatedphotodynamictherapycanbephotobiomodulatedwith808nmlight
AT georgeswagnieres autophagyandapoptosisinducedinu87mgglioblastomacellsbyhypericinmediatedphotodynamictherapycanbephotobiomodulatedwith808nmlight
AT veronikahuntosova autophagyandapoptosisinducedinu87mgglioblastomacellsbyhypericinmediatedphotodynamictherapycanbephotobiomodulatedwith808nmlight
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