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Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death

BACKGROUND: Disulfiram (DSF), which is used to treat alcohol dependence, has been reported to have anti-cancer effects in various malignant tumors. In this study, we investigated the anti-cancer effects and mechanism of DSF in HNSCC. METHODS: Head and neck squamous carcinoma cell lines (FaDu and Hep...

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Autores principales: Park, Young Min, Go, Yoon Young, Shin, Sun Hwa, Cho, Jae-Gu, Woo, Jeong-Soo, Song, Jae-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136695/
https://www.ncbi.nlm.nih.gov/pubmed/30212479
http://dx.doi.org/10.1371/journal.pone.0203069
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author Park, Young Min
Go, Yoon Young
Shin, Sun Hwa
Cho, Jae-Gu
Woo, Jeong-Soo
Song, Jae-Jun
author_facet Park, Young Min
Go, Yoon Young
Shin, Sun Hwa
Cho, Jae-Gu
Woo, Jeong-Soo
Song, Jae-Jun
author_sort Park, Young Min
collection PubMed
description BACKGROUND: Disulfiram (DSF), which is used to treat alcohol dependence, has been reported to have anti-cancer effects in various malignant tumors. In this study, we investigated the anti-cancer effects and mechanism of DSF in HNSCC. METHODS: Head and neck squamous carcinoma cell lines (FaDu and Hep2) were used to analyze the anti-cancer effects of DSF. The anti-cancer effects of DSF were confirmed in vivo using a xenograft tumor model. RESULTS: The anti-cancer effects of DSF in HNSCC were found to be copper (Cu) dependent. Specifically, DSF/Cu markedly inhibited HNSCC at a concentration of 1 μM. After DSF/Cu administration, production of reactive oxygen species (ROS) was remarkable starting at 0.5 μM, suggesting that the inhibitory effects of DSF/Cu on HNSCC are mediated through the formation of ROS. The levels of phospho-JNK, phospho-cJun and phospho-p38 were increased after DSF/Cu treatment while levels of phospho-Akt were decreased. These results suggested that the inhibitory effects of DSF/Cu on HNSCC cells involve ROS formation and down-regulation of Akt-signaling. Through these molecular mechanisms, DSF ultimately induce the inhibitory effects on HNSCC cell lines mainly through autophagic cell death, not apoptotic cell death. Lastly, we investigated the clinical relevance of DSF/Cu using a HNSCC xenograft animal model, which showed that tumor growth was remarkably decreased by DSF (50 mg/kg injection). CONCLUSION: In treating patients with HNSCC, DSF may contribute to improved HNSCC patient’s survival. The characteristic anti-cancer effects of DSF on HNSCC may suggest new therapeutic potential for this medication in HNSCC patients.
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spelling pubmed-61366952018-09-27 Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death Park, Young Min Go, Yoon Young Shin, Sun Hwa Cho, Jae-Gu Woo, Jeong-Soo Song, Jae-Jun PLoS One Research Article BACKGROUND: Disulfiram (DSF), which is used to treat alcohol dependence, has been reported to have anti-cancer effects in various malignant tumors. In this study, we investigated the anti-cancer effects and mechanism of DSF in HNSCC. METHODS: Head and neck squamous carcinoma cell lines (FaDu and Hep2) were used to analyze the anti-cancer effects of DSF. The anti-cancer effects of DSF were confirmed in vivo using a xenograft tumor model. RESULTS: The anti-cancer effects of DSF in HNSCC were found to be copper (Cu) dependent. Specifically, DSF/Cu markedly inhibited HNSCC at a concentration of 1 μM. After DSF/Cu administration, production of reactive oxygen species (ROS) was remarkable starting at 0.5 μM, suggesting that the inhibitory effects of DSF/Cu on HNSCC are mediated through the formation of ROS. The levels of phospho-JNK, phospho-cJun and phospho-p38 were increased after DSF/Cu treatment while levels of phospho-Akt were decreased. These results suggested that the inhibitory effects of DSF/Cu on HNSCC cells involve ROS formation and down-regulation of Akt-signaling. Through these molecular mechanisms, DSF ultimately induce the inhibitory effects on HNSCC cell lines mainly through autophagic cell death, not apoptotic cell death. Lastly, we investigated the clinical relevance of DSF/Cu using a HNSCC xenograft animal model, which showed that tumor growth was remarkably decreased by DSF (50 mg/kg injection). CONCLUSION: In treating patients with HNSCC, DSF may contribute to improved HNSCC patient’s survival. The characteristic anti-cancer effects of DSF on HNSCC may suggest new therapeutic potential for this medication in HNSCC patients. Public Library of Science 2018-09-13 /pmc/articles/PMC6136695/ /pubmed/30212479 http://dx.doi.org/10.1371/journal.pone.0203069 Text en © 2018 Park et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Park, Young Min
Go, Yoon Young
Shin, Sun Hwa
Cho, Jae-Gu
Woo, Jeong-Soo
Song, Jae-Jun
Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
title Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
title_full Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
title_fullStr Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
title_full_unstemmed Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
title_short Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
title_sort anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136695/
https://www.ncbi.nlm.nih.gov/pubmed/30212479
http://dx.doi.org/10.1371/journal.pone.0203069
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