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Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells
Salicylamide, a non-steroidal anti-inflammatory drug (NSAID), is used as an analgesic and antipyretic agent. We have previously shown that several NSAIDs have anti-melanogenic properties in B16F1 melanoma cells. In contrast, we have found that salicylamide enhances melanin contents in B16F1 melanoma...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Applied Pharmacology
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255140/ https://www.ncbi.nlm.nih.gov/pubmed/33731492 http://dx.doi.org/10.4062/biomolther.2020.222 |
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author | Ito, Yusuke Sato, Kazuomi |
author_facet | Ito, Yusuke Sato, Kazuomi |
author_sort | Ito, Yusuke |
collection | PubMed |
description | Salicylamide, a non-steroidal anti-inflammatory drug (NSAID), is used as an analgesic and antipyretic agent. We have previously shown that several NSAIDs have anti-melanogenic properties in B16F1 melanoma cells. In contrast, we have found that salicylamide enhances melanin contents in B16F1 melanoma cells; however, the underlying mechanism is not known. Therefore, we investigated the mechanism through which salicylamide stimulates melanogenesis. Interestingly, salicylamide enhanced diphenolase activity in a cell-free assay. Western blotting and real-time RT-PCR revealed that salicylamide increased tyrosinase expression via transcriptional activation of the Mitf gene. Together, our results indicate that salicylamide could be used as an anti-hypopigmentation agent for skin and/or hair. |
format | Online Article Text |
id | pubmed-8255140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-82551402021-07-09 Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells Ito, Yusuke Sato, Kazuomi Biomol Ther (Seoul) Original Article Salicylamide, a non-steroidal anti-inflammatory drug (NSAID), is used as an analgesic and antipyretic agent. We have previously shown that several NSAIDs have anti-melanogenic properties in B16F1 melanoma cells. In contrast, we have found that salicylamide enhances melanin contents in B16F1 melanoma cells; however, the underlying mechanism is not known. Therefore, we investigated the mechanism through which salicylamide stimulates melanogenesis. Interestingly, salicylamide enhanced diphenolase activity in a cell-free assay. Western blotting and real-time RT-PCR revealed that salicylamide increased tyrosinase expression via transcriptional activation of the Mitf gene. Together, our results indicate that salicylamide could be used as an anti-hypopigmentation agent for skin and/or hair. The Korean Society of Applied Pharmacology 2021-07-01 2021-03-17 /pmc/articles/PMC8255140/ /pubmed/33731492 http://dx.doi.org/10.4062/biomolther.2020.222 Text en Copyright © 2021, The Korean Society of Applied Pharmacology https://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 (https://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 Ito, Yusuke Sato, Kazuomi Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells |
title | Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells |
title_full | Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells |
title_fullStr | Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells |
title_full_unstemmed | Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells |
title_short | Salicylamide Enhances Melanin Synthesis in B16F1 Melanoma Cells |
title_sort | salicylamide enhances melanin synthesis in b16f1 melanoma cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255140/ https://www.ncbi.nlm.nih.gov/pubmed/33731492 http://dx.doi.org/10.4062/biomolther.2020.222 |
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