Ketoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes

Malignant melanoma is responsible for the majority of skin cancer-related deaths. The methods of cancer treatment include surgical removal, chemotherapy, immunotherapy, and targeted therapy. However, neither of these methods gives satisfactory results. Therefore, the development of new anticancer th...

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Autores principales: Klaudia Banach, Justyna Kowalska, Zuzanna Rzepka, Artur Beberok, Jakub Rok, Dorota Wrześniok
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:e3ea8656673249caa07738f09854b4312021-11-11T17:23:18ZKetoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes10.3390/ijms2221119661422-00671661-6596https://doaj.org/article/e3ea8656673249caa07738f09854b4312021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/21/11966https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Malignant melanoma is responsible for the majority of skin cancer-related deaths. The methods of cancer treatment include surgical removal, chemotherapy, immunotherapy, and targeted therapy. However, neither of these methods gives satisfactory results. Therefore, the development of new anticancer therapeutic strategies is very important and may extend the life span of people suffering from melanoma. The aim of this study was to examine the effect of ketoprofen (KTP) and UVA radiation (UVAR) therapy on cell proliferation, apoptosis, and cell cycle distribution in both melanotic melanoma cells (COLO829) and human melanocytes (HEMn-DP) in relation to its supportive effect in the treatment of melanoma. The therapy combining the use of pre-incubation with KTP and UVAR causes a significant increase in the anti-proliferative properties of ketoprofen towards melanoma cells and the co-exposure of melanotic melanoma cells induced apoptosis shown as the mitochondrial membrane breakdown, cell-cycle deregulation, and DNA fragmentation. Moreover, co-treatment led to GSH depletion showing its pro-apoptotic effect dependent on ROS overproduction. The treatment did not show a significant effect on normal cells—melanocytes—which indicates its high selectivity. The results suggest a possible benefit from the use of the ketoprofen and ultraviolet A irradiation as a new concept of melanotic melanoma therapy.Klaudia BanachJustyna KowalskaZuzanna RzepkaArtur BeberokJakub RokDorota WrześniokMDPI AGarticlemelanotic melanomaUVA radiationketoprofenmelanocytesCOLO829Biology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 11966, p 11966 (2021)
institution DOAJ
collection DOAJ
language EN
topic melanotic melanoma
UVA radiation
ketoprofen
melanocytes
COLO829
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle melanotic melanoma
UVA radiation
ketoprofen
melanocytes
COLO829
Biology (General)
QH301-705.5
Chemistry
QD1-999
Klaudia Banach
Justyna Kowalska
Zuzanna Rzepka
Artur Beberok
Jakub Rok
Dorota Wrześniok
Ketoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes
description Malignant melanoma is responsible for the majority of skin cancer-related deaths. The methods of cancer treatment include surgical removal, chemotherapy, immunotherapy, and targeted therapy. However, neither of these methods gives satisfactory results. Therefore, the development of new anticancer therapeutic strategies is very important and may extend the life span of people suffering from melanoma. The aim of this study was to examine the effect of ketoprofen (KTP) and UVA radiation (UVAR) therapy on cell proliferation, apoptosis, and cell cycle distribution in both melanotic melanoma cells (COLO829) and human melanocytes (HEMn-DP) in relation to its supportive effect in the treatment of melanoma. The therapy combining the use of pre-incubation with KTP and UVAR causes a significant increase in the anti-proliferative properties of ketoprofen towards melanoma cells and the co-exposure of melanotic melanoma cells induced apoptosis shown as the mitochondrial membrane breakdown, cell-cycle deregulation, and DNA fragmentation. Moreover, co-treatment led to GSH depletion showing its pro-apoptotic effect dependent on ROS overproduction. The treatment did not show a significant effect on normal cells—melanocytes—which indicates its high selectivity. The results suggest a possible benefit from the use of the ketoprofen and ultraviolet A irradiation as a new concept of melanotic melanoma therapy.
format article
author Klaudia Banach
Justyna Kowalska
Zuzanna Rzepka
Artur Beberok
Jakub Rok
Dorota Wrześniok
author_facet Klaudia Banach
Justyna Kowalska
Zuzanna Rzepka
Artur Beberok
Jakub Rok
Dorota Wrześniok
author_sort Klaudia Banach
title Ketoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes
title_short Ketoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes
title_full Ketoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes
title_fullStr Ketoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes
title_full_unstemmed Ketoprofen Combined with UVA Irradiation Exerts Higher Selectivity in the Mode of Action against Melanotic Melanoma Cells than against Normal Human Melanocytes
title_sort ketoprofen combined with uva irradiation exerts higher selectivity in the mode of action against melanotic melanoma cells than against normal human melanocytes
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/e3ea8656673249caa07738f09854b431
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