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The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma
Melanoma is the most common form of skin cancer. Given its high mortality, the interest in the search of preventive measures, such as dietary factors, is growing significantly. In this study we tested, in vitro and in vivo, the potential anti-cancer effect of the acetyl deacylasadisulfide (ADA), a v...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326790/ https://www.ncbi.nlm.nih.gov/pubmed/28289382 http://dx.doi.org/10.3389/fphar.2017.00065 |
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author | De Cicco, Paola Panza, Elisabetta Armogida, Chiara Ercolano, Giuseppe Taglialatela-Scafati, Orazio Shokoohinia, Yalda Camerlingo, Rosa Pirozzi, Giuseppe Calderone, Vincenzo Cirino, Giuseppe Ianaro, Angela |
author_facet | De Cicco, Paola Panza, Elisabetta Armogida, Chiara Ercolano, Giuseppe Taglialatela-Scafati, Orazio Shokoohinia, Yalda Camerlingo, Rosa Pirozzi, Giuseppe Calderone, Vincenzo Cirino, Giuseppe Ianaro, Angela |
author_sort | De Cicco, Paola |
collection | PubMed |
description | Melanoma is the most common form of skin cancer. Given its high mortality, the interest in the search of preventive measures, such as dietary factors, is growing significantly. In this study we tested, in vitro and in vivo, the potential anti-cancer effect of the acetyl deacylasadisulfide (ADA), a vinyl disulfide compound, isolated and purified from asafoetida a foul-smelling oleo gum-resin of dietary and medicinal relevance. ADA markedly suppressed proliferation of human melanoma cell lines by inducing apoptosis. Moreover, treatment of melanoma cells with ADA reduced nuclear translocation and activation of NF-κB, decreased the expression of the anti-apoptotic proteins c-FLIP, XIAP, and Bcl-2 and inhibited the phosphorylation and activation of both AKT and ERK proteins, two of the most frequently deregulated pathways in melanoma. Finally, the results obtained in vitro were substantiated by the findings that ADA significantly and dose-dependently reduced lung metastatic foci formation in C57BL/6 mice. In conclusion, our findings suggest that ADA significantly inhibits melanoma progression in vivo and could represent an important lead compound for the development of new anti-metastatic agents. |
format | Online Article Text |
id | pubmed-5326790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53267902017-03-13 The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma De Cicco, Paola Panza, Elisabetta Armogida, Chiara Ercolano, Giuseppe Taglialatela-Scafati, Orazio Shokoohinia, Yalda Camerlingo, Rosa Pirozzi, Giuseppe Calderone, Vincenzo Cirino, Giuseppe Ianaro, Angela Front Pharmacol Pharmacology Melanoma is the most common form of skin cancer. Given its high mortality, the interest in the search of preventive measures, such as dietary factors, is growing significantly. In this study we tested, in vitro and in vivo, the potential anti-cancer effect of the acetyl deacylasadisulfide (ADA), a vinyl disulfide compound, isolated and purified from asafoetida a foul-smelling oleo gum-resin of dietary and medicinal relevance. ADA markedly suppressed proliferation of human melanoma cell lines by inducing apoptosis. Moreover, treatment of melanoma cells with ADA reduced nuclear translocation and activation of NF-κB, decreased the expression of the anti-apoptotic proteins c-FLIP, XIAP, and Bcl-2 and inhibited the phosphorylation and activation of both AKT and ERK proteins, two of the most frequently deregulated pathways in melanoma. Finally, the results obtained in vitro were substantiated by the findings that ADA significantly and dose-dependently reduced lung metastatic foci formation in C57BL/6 mice. In conclusion, our findings suggest that ADA significantly inhibits melanoma progression in vivo and could represent an important lead compound for the development of new anti-metastatic agents. Frontiers Media S.A. 2017-02-27 /pmc/articles/PMC5326790/ /pubmed/28289382 http://dx.doi.org/10.3389/fphar.2017.00065 Text en Copyright © 2017 De Cicco, Panza, Armogida, Ercolano, Taglialatela-Scafati, Shokoohinia, Camerlingo, Pirozzi, Calderone, Cirino and Ianaro. http://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) or licensor 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 | Pharmacology De Cicco, Paola Panza, Elisabetta Armogida, Chiara Ercolano, Giuseppe Taglialatela-Scafati, Orazio Shokoohinia, Yalda Camerlingo, Rosa Pirozzi, Giuseppe Calderone, Vincenzo Cirino, Giuseppe Ianaro, Angela The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma |
title | The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma |
title_full | The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma |
title_fullStr | The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma |
title_full_unstemmed | The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma |
title_short | The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma |
title_sort | hydrogen sulfide releasing molecule acetyl deacylasadisulfide inhibits metastatic melanoma |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326790/ https://www.ncbi.nlm.nih.gov/pubmed/28289382 http://dx.doi.org/10.3389/fphar.2017.00065 |
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