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Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments

BACKGROUND: Total annual cancer rates have decreased due to improved treatment and prevention. However, the incidence of melanoma is rising, and not all patients respond to immune and targeted approaches. Therefore, we sought to determine the efficacy of red light (RL) phototherapy in preclinical mo...

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Autores principales: Austin, Evan, Huang, Alisen, Wang, Jennifer Y., Cohen, Marc, Heilman, Edward, Maverakis, Emanual, Michl, Josef, Jagdeo, Jared
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9278815/
https://www.ncbi.nlm.nih.gov/pubmed/35847848
http://dx.doi.org/10.3389/fonc.2022.928484
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author Austin, Evan
Huang, Alisen
Wang, Jennifer Y.
Cohen, Marc
Heilman, Edward
Maverakis, Emanual
Michl, Josef
Jagdeo, Jared
author_facet Austin, Evan
Huang, Alisen
Wang, Jennifer Y.
Cohen, Marc
Heilman, Edward
Maverakis, Emanual
Michl, Josef
Jagdeo, Jared
author_sort Austin, Evan
collection PubMed
description BACKGROUND: Total annual cancer rates have decreased due to improved treatment and prevention. However, the incidence of melanoma is rising, and not all patients respond to immune and targeted approaches. Therefore, we sought to determine the efficacy of red light (RL) phototherapy in preclinical models of melanoma. METHODS: Melanoma cells (A375, B16F10, MNT-1) were irradiated with RL. Melanoma proliferation, apoptosis, oxidative stress, and p53 phosphorylation were measured in vitro. In C57BL/6 mice, phototherapy safety, B16F10 tumor growth, and immunocyte infiltration were assessed following RL. RESULTS: In vitro, 640 J/cm(2) RL decreased cellular proliferation without increasing apoptosis, while 1280 J/cm(2) increased apoptosis. RL increased intracellular reactive oxygen species generation and p53 phosphorylation. In animal models, 2560 J/cm(2) RL significantly prevented melanoma growth and increased the expression of CD103+ dendritic cells. 1280 and 1920 J/cm(2) RL decreased tumor volume, but not significantly. RL did not cause skin inflammation or erythema in normal skin. CONCLUSION: RL represents a potentially safe and effective melanoma therapeutic. RL prevented tumor growth and increased the expression of immune markers, such as CD103, that are associated with favorable melanoma outcomes. Further research is needed to determine the optimal clinical treatment regimen for melanoma using RL.
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spelling pubmed-92788152022-07-14 Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments Austin, Evan Huang, Alisen Wang, Jennifer Y. Cohen, Marc Heilman, Edward Maverakis, Emanual Michl, Josef Jagdeo, Jared Front Oncol Oncology BACKGROUND: Total annual cancer rates have decreased due to improved treatment and prevention. However, the incidence of melanoma is rising, and not all patients respond to immune and targeted approaches. Therefore, we sought to determine the efficacy of red light (RL) phototherapy in preclinical models of melanoma. METHODS: Melanoma cells (A375, B16F10, MNT-1) were irradiated with RL. Melanoma proliferation, apoptosis, oxidative stress, and p53 phosphorylation were measured in vitro. In C57BL/6 mice, phototherapy safety, B16F10 tumor growth, and immunocyte infiltration were assessed following RL. RESULTS: In vitro, 640 J/cm(2) RL decreased cellular proliferation without increasing apoptosis, while 1280 J/cm(2) increased apoptosis. RL increased intracellular reactive oxygen species generation and p53 phosphorylation. In animal models, 2560 J/cm(2) RL significantly prevented melanoma growth and increased the expression of CD103+ dendritic cells. 1280 and 1920 J/cm(2) RL decreased tumor volume, but not significantly. RL did not cause skin inflammation or erythema in normal skin. CONCLUSION: RL represents a potentially safe and effective melanoma therapeutic. RL prevented tumor growth and increased the expression of immune markers, such as CD103, that are associated with favorable melanoma outcomes. Further research is needed to determine the optimal clinical treatment regimen for melanoma using RL. Frontiers Media S.A. 2022-06-24 /pmc/articles/PMC9278815/ /pubmed/35847848 http://dx.doi.org/10.3389/fonc.2022.928484 Text en Copyright © 2022 Austin, Huang, Wang, Cohen, Heilman, Maverakis, Michl and Jagdeo https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Austin, Evan
Huang, Alisen
Wang, Jennifer Y.
Cohen, Marc
Heilman, Edward
Maverakis, Emanual
Michl, Josef
Jagdeo, Jared
Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments
title Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments
title_full Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments
title_fullStr Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments
title_full_unstemmed Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments
title_short Red Light Phototherapy Using Light-Emitting Diodes Inhibits Melanoma Proliferation and Alters Tumor Microenvironments
title_sort red light phototherapy using light-emitting diodes inhibits melanoma proliferation and alters tumor microenvironments
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9278815/
https://www.ncbi.nlm.nih.gov/pubmed/35847848
http://dx.doi.org/10.3389/fonc.2022.928484
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