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The Hydrogen Sulfide Releasing Molecule Acetyl Deacylasadisulfide Inhibits Metastatic Melanoma
Paola De Cicco1, Elisabetta Panza1, Chiara Armogida1
1Department of Pharmacy, University of Naples Federico II Naples, Italy.
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.
Insights
Acetyl deacylasadisulfide (ADA) from asafoetida shows anti-melanoma properties. This dietary compound suppressed melanoma cell growth and reduced lung metastasis in mice, suggesting potential as an anti-cancer agent.
Area of Science:
- Oncology
- Pharmacology
- Natural Products Chemistry
Background:
- Melanoma is a prevalent and deadly skin cancer.
- Preventive strategies, including dietary factors, are increasingly sought.
- Asafoetida, a dietary oleo gum-resin, contains bioactive compounds.
Purpose of the Study:
- To investigate the anti-cancer effects of acetyl deacylasadisulfide (ADA), a compound from asafoetida.
- To evaluate ADA's efficacy against human melanoma cells both in vitro and in vivo.
Main Methods:
- In vitro studies using human melanoma cell lines.
- In vivo studies involving C57BL/6 mice with induced lung metastatic foci.
- Analysis of molecular pathways including NF-κB, AKT, and ERK signaling.
Main Results:
- ADA significantly suppressed melanoma cell proliferation by inducing apoptosis.
- ADA inhibited key pro-survival and pro-metastatic signaling pathways (NF-κB, AKT, ERK).
- ADA dose-dependently reduced lung metastasis formation in mice.
Conclusions:
- ADA exhibits significant anti-melanoma and anti-metastatic activity.
- ADA demonstrates potential as a lead compound for novel anti-cancer drug development.
- Dietary compounds like ADA warrant further investigation for cancer prevention and treatment.
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