Back to Search Start Over

The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma

Authors :
Angela Ianaro
Orazio Taglialatela-Scafati
Yalda Shokoohinia
Vincenzo Calderone
Elisabetta Panza
Rosa Camerlingo
Chiara Armogida
Giuseppe Pirozzi
Giuseppe Ercolano
Paola De Cicco
Giuseppe Cirino
DE CICCO, Paola
Panza, Elisabetta
Armogida, Chiara
Ercolano, Giuseppe
TAGLIALATELA SCAFATI, Orazio
Shokoohinia, Yalda
Camerlingo, Rosa
Pirozzi, Giuseppe
Calderone, Vincenzo
Cirino, Giuseppe
Ianaro, Angela
Source :
Frontiers in Pharmacology
Publication Year :
2017
Publisher :
Frontiers Media S.A., 2017.

Abstract

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.

Details

Language :
English
ISSN :
16639812
Volume :
8
Database :
OpenAIRE
Journal :
Frontiers in Pharmacology
Accession number :
edsair.doi.dedup.....6bc64437faeb6a57351d5f1b7c702a60
Full Text :
https://doi.org/10.3389/fphar.2017.00065