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The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells
The anticancer activity of disulfiram (DS) is copper(ii) (Cu)-dependent. This study investigated the anticancer mechanisms of DS/Cu using in vitro cytotoxicity and metabolic kinetic analysis. Our study indicates that DS/Cu targets cancer cells by the combination of two types of actions: (1) instant...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027600/ https://www.ncbi.nlm.nih.gov/pubmed/27708770 http://dx.doi.org/10.1039/c5tx00210a |
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author | Tawari, Patricia Erebi Wang, Zhipeng Najlah, Mohammad Tsang, Chi Wai Kannappan, Vinodh Liu, Peng McConville, Christopher He, Bin Armesilla, Angel L. Wang, Weiguang |
author_facet | Tawari, Patricia Erebi Wang, Zhipeng Najlah, Mohammad Tsang, Chi Wai Kannappan, Vinodh Liu, Peng McConville, Christopher He, Bin Armesilla, Angel L. Wang, Weiguang |
author_sort | Tawari, Patricia Erebi |
collection | PubMed |
description | The anticancer activity of disulfiram (DS) is copper(ii) (Cu)-dependent. This study investigated the anticancer mechanisms of DS/Cu using in vitro cytotoxicity and metabolic kinetic analysis. Our study indicates that DS/Cu targets cancer cells by the combination of two types of actions: (1) instant killing executed by DS/Cu reaction generated reactive oxygen species; (2) delayed cytotoxicity introduced by the end product, DDC-Cu. Nanoencapsulation of DS might shed light on repositioning of DS into cancer treatment. |
format | Online Article Text |
id | pubmed-5027600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-50276002016-10-03 The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells Tawari, Patricia Erebi Wang, Zhipeng Najlah, Mohammad Tsang, Chi Wai Kannappan, Vinodh Liu, Peng McConville, Christopher He, Bin Armesilla, Angel L. Wang, Weiguang Toxicol Res (Camb) Chemistry The anticancer activity of disulfiram (DS) is copper(ii) (Cu)-dependent. This study investigated the anticancer mechanisms of DS/Cu using in vitro cytotoxicity and metabolic kinetic analysis. Our study indicates that DS/Cu targets cancer cells by the combination of two types of actions: (1) instant killing executed by DS/Cu reaction generated reactive oxygen species; (2) delayed cytotoxicity introduced by the end product, DDC-Cu. Nanoencapsulation of DS might shed light on repositioning of DS into cancer treatment. Royal Society of Chemistry 2015-11-19 2015-09-10 /pmc/articles/PMC5027600/ /pubmed/27708770 http://dx.doi.org/10.1039/c5tx00210a Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Tawari, Patricia Erebi Wang, Zhipeng Najlah, Mohammad Tsang, Chi Wai Kannappan, Vinodh Liu, Peng McConville, Christopher He, Bin Armesilla, Angel L. Wang, Weiguang The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells |
title | The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells |
title_full | The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells |
title_fullStr | The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells |
title_full_unstemmed | The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells |
title_short | The cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells |
title_sort | cytotoxic mechanisms of disulfiram and copper(ii) in cancer cells |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027600/ https://www.ncbi.nlm.nih.gov/pubmed/27708770 http://dx.doi.org/10.1039/c5tx00210a |
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