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Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells
Melatonin plays different physiological functions ranging from the regulation of circadian rhythms to tumor inhibition, owing to its antioxidant, immunomodulatory and anti-aging properties. Due to its pleiotropic functions, melatonin has been shown to elicit cytoprotective processes in normal cells...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620261/ https://www.ncbi.nlm.nih.gov/pubmed/28978121 http://dx.doi.org/10.18632/oncotarget.20124 |
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author | Gatti, Giuliana Lucini, Valeria Dugnani, Silvana Calastretti, Angela Spadoni, Gilberto Bedini, Annalida Rivara, Silvia Mor, Marco Canti, Gianfranco Scaglione, Francesco Bevilacqua, Annamaria |
author_facet | Gatti, Giuliana Lucini, Valeria Dugnani, Silvana Calastretti, Angela Spadoni, Gilberto Bedini, Annalida Rivara, Silvia Mor, Marco Canti, Gianfranco Scaglione, Francesco Bevilacqua, Annamaria |
author_sort | Gatti, Giuliana |
collection | PubMed |
description | Melatonin plays different physiological functions ranging from the regulation of circadian rhythms to tumor inhibition, owing to its antioxidant, immunomodulatory and anti-aging properties. Due to its pleiotropic functions, melatonin has been shown to elicit cytoprotective processes in normal cells and trigger pro-apoptotic signals in cancer cells. The therapeutic potential of melatonin analogues prompted us to investigate the in vitro and in vivo antitumor activity of new melatonin derivatives and explore the underlying molecular mechanisms. The experiments revealed that the new melatonin analogues inhibited the growth of melanoma and breast cancer cells in a dose- and time-dependent manner. In addition, our results indicated that melatonin derivative UCM 1037 could induce apoptosis in melanoma and breast cancer cells, as well as cell necrosis, in MCF-7. Together, apoptosis and necrosis could be two possible mechanisms to explain the cytotoxic effect of the melatonin analogue against cancer cells. The suppression of tumor growth by the melatonin analogues was further demonstrated in vivo in a xenograft mice model. A decrease in the activation of MAPK pathway was observed in all cancer cells following UCM 1037 treatment. Overall, this study describes a promising antitumor compound showing antiproliferative and cytotoxic activity in melanoma and breast cancer cells. |
format | Online Article Text |
id | pubmed-5620261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56202612017-10-03 Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells Gatti, Giuliana Lucini, Valeria Dugnani, Silvana Calastretti, Angela Spadoni, Gilberto Bedini, Annalida Rivara, Silvia Mor, Marco Canti, Gianfranco Scaglione, Francesco Bevilacqua, Annamaria Oncotarget Research Paper Melatonin plays different physiological functions ranging from the regulation of circadian rhythms to tumor inhibition, owing to its antioxidant, immunomodulatory and anti-aging properties. Due to its pleiotropic functions, melatonin has been shown to elicit cytoprotective processes in normal cells and trigger pro-apoptotic signals in cancer cells. The therapeutic potential of melatonin analogues prompted us to investigate the in vitro and in vivo antitumor activity of new melatonin derivatives and explore the underlying molecular mechanisms. The experiments revealed that the new melatonin analogues inhibited the growth of melanoma and breast cancer cells in a dose- and time-dependent manner. In addition, our results indicated that melatonin derivative UCM 1037 could induce apoptosis in melanoma and breast cancer cells, as well as cell necrosis, in MCF-7. Together, apoptosis and necrosis could be two possible mechanisms to explain the cytotoxic effect of the melatonin analogue against cancer cells. The suppression of tumor growth by the melatonin analogues was further demonstrated in vivo in a xenograft mice model. A decrease in the activation of MAPK pathway was observed in all cancer cells following UCM 1037 treatment. Overall, this study describes a promising antitumor compound showing antiproliferative and cytotoxic activity in melanoma and breast cancer cells. Impact Journals LLC 2017-08-10 /pmc/articles/PMC5620261/ /pubmed/28978121 http://dx.doi.org/10.18632/oncotarget.20124 Text en Copyright: © 2017 Gatti et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Gatti, Giuliana Lucini, Valeria Dugnani, Silvana Calastretti, Angela Spadoni, Gilberto Bedini, Annalida Rivara, Silvia Mor, Marco Canti, Gianfranco Scaglione, Francesco Bevilacqua, Annamaria Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells |
title | Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells |
title_full | Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells |
title_fullStr | Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells |
title_full_unstemmed | Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells |
title_short | Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells |
title_sort | antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620261/ https://www.ncbi.nlm.nih.gov/pubmed/28978121 http://dx.doi.org/10.18632/oncotarget.20124 |
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