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Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate
Sodium 2-mercaptoethanesulfonate (mesna) is a protective agent that is widely used in medicine because of its antioxidant effects. Recently, reactive oxygen species (ROS) were shown to increase pigmentation. Thus, ROS scavengers and inhibitors of ROS production may suppress melanogenesis. Forkhead b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Physiological Society and The Korean Society of Pharmacology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043997/ https://www.ncbi.nlm.nih.gov/pubmed/32140038 http://dx.doi.org/10.4196/kjpp.2020.24.2.149 |
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author | Kim, Jeong-Hwan Oh, Chang-Taek Kwon, Tae-Rin Kim, Jong Hwan Bak, Dong-Ho Kim, Hyuk Park, Won-Seok Kim, Beom Joon |
author_facet | Kim, Jeong-Hwan Oh, Chang-Taek Kwon, Tae-Rin Kim, Jong Hwan Bak, Dong-Ho Kim, Hyuk Park, Won-Seok Kim, Beom Joon |
author_sort | Kim, Jeong-Hwan |
collection | PubMed |
description | Sodium 2-mercaptoethanesulfonate (mesna) is a protective agent that is widely used in medicine because of its antioxidant effects. Recently, reactive oxygen species (ROS) were shown to increase pigmentation. Thus, ROS scavengers and inhibitors of ROS production may suppress melanogenesis. Forkhead box-O3a (FoxO3a) is an antimelanogenic factor that mediates ROS-induced skin pigmentation. In this study, we aimed to investigate the whitening effect of mesna and the signaling mechanism mediating this effect. Human melanoma (MNT-1) cells were used in this study. mRNA and protein expression were measured by real-time quantitative PCR and Western blotting analysis to track changes in FoxO3a-related signals induced by mesna. An immunofluorescence assay was performed to determine the nuclear translocation of FoxO3a. When MNT-1 melanoma cells were treated with mesna, melanin production and secretion decreased. These effects were accompanied by increases in FoxO3a activation and nuclear translocation, resulting in downregulation of four master genes of melanogenesis: MITF, TYR, TRP1, and TRP2. We found that mesna, an antioxidant and radical scavenger, suppresses melanin production and may therefore be a useful agent for the clinical treatment of hyperpigmentation disorders. |
format | Online Article Text |
id | pubmed-7043997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Physiological Society and The Korean Society of Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-70439972020-03-06 Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate Kim, Jeong-Hwan Oh, Chang-Taek Kwon, Tae-Rin Kim, Jong Hwan Bak, Dong-Ho Kim, Hyuk Park, Won-Seok Kim, Beom Joon Korean J Physiol Pharmacol Original Article Sodium 2-mercaptoethanesulfonate (mesna) is a protective agent that is widely used in medicine because of its antioxidant effects. Recently, reactive oxygen species (ROS) were shown to increase pigmentation. Thus, ROS scavengers and inhibitors of ROS production may suppress melanogenesis. Forkhead box-O3a (FoxO3a) is an antimelanogenic factor that mediates ROS-induced skin pigmentation. In this study, we aimed to investigate the whitening effect of mesna and the signaling mechanism mediating this effect. Human melanoma (MNT-1) cells were used in this study. mRNA and protein expression were measured by real-time quantitative PCR and Western blotting analysis to track changes in FoxO3a-related signals induced by mesna. An immunofluorescence assay was performed to determine the nuclear translocation of FoxO3a. When MNT-1 melanoma cells were treated with mesna, melanin production and secretion decreased. These effects were accompanied by increases in FoxO3a activation and nuclear translocation, resulting in downregulation of four master genes of melanogenesis: MITF, TYR, TRP1, and TRP2. We found that mesna, an antioxidant and radical scavenger, suppresses melanin production and may therefore be a useful agent for the clinical treatment of hyperpigmentation disorders. The Korean Physiological Society and The Korean Society of Pharmacology 2020-03 2020-02-20 /pmc/articles/PMC7043997/ /pubmed/32140038 http://dx.doi.org/10.4196/kjpp.2020.24.2.149 Text en Copyright © Korean J Physiol Pharmacol http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Jeong-Hwan Oh, Chang-Taek Kwon, Tae-Rin Kim, Jong Hwan Bak, Dong-Ho Kim, Hyuk Park, Won-Seok Kim, Beom Joon Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate |
title | Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate |
title_full | Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate |
title_fullStr | Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate |
title_full_unstemmed | Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate |
title_short | Inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate |
title_sort | inhibition of melanogenesis by sodium 2-mercaptoethanesulfonate |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043997/ https://www.ncbi.nlm.nih.gov/pubmed/32140038 http://dx.doi.org/10.4196/kjpp.2020.24.2.149 |
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