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Auranofin: Repurposing an Old Drug for a Golden New Age
Drug discovery, development and registration is an expensive and time-consuming process associated with a high failure rate [Pessetto et al. (Mol Cancer Ther 12:1299–1309, 2013), Woodcock and Woosley (Annu Rev Med 59:1–12, 2008)]. Drug ‘repurposing’ is the identification of new therapeutic purposes...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359176/ https://www.ncbi.nlm.nih.gov/pubmed/25698589 http://dx.doi.org/10.1007/s40268-015-0083-y |
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author | Roder, Christine Thomson, Melanie J. |
author_facet | Roder, Christine Thomson, Melanie J. |
author_sort | Roder, Christine |
collection | PubMed |
description | Drug discovery, development and registration is an expensive and time-consuming process associated with a high failure rate [Pessetto et al. (Mol Cancer Ther 12:1299–1309, 2013), Woodcock and Woosley (Annu Rev Med 59:1–12, 2008)]. Drug ‘repurposing’ is the identification of new therapeutic purposes for already approved drugs and is more affordable and achievable than novel drug discovery [Pessetto et al. (Mol Cancer Ther 12:1299–1309, 2013)]. Auranofin is a drug that is approved for the treatment of rheumatoid arthritis but is being investigated for potential therapeutic application in a number of other diseases including cancer, neurodegenerative disorders, HIV/AIDS, parasitic infections and bacterial infections [Tejman-Yarden et al. (Antimicrob Agents Chemother 57:2029–2035, 2013)]. The main mechanism of action of auranofin is through the inhibition of reduction/oxidation (redox) enzymes that are essential for maintaining intracellular levels of reactive oxygen species. Inhibition of these enzymes leads to cellular oxidative stress and intrinsic apoptosis [Pessetto et al. (Mol Cancer Ther 12:1299–1309, 2013), Fan et al. (Cell Death Dis 5:e1191, 2014), Fiskus et al. (Cancer Res 74:2520–2532, 2014), Marzano et al. (Free Radic Biol Med 42:872–881, 2007)]. Drugs such as auranofin that have already been approved for human use [Tejman-Yarden et al. (Antimicrob Agents Chemother 57:2029–2035, 2013)] can be brought into clinical use for other diseases relatively quickly and for a fraction of the cost of new drugs. |
format | Online Article Text |
id | pubmed-4359176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-43591762015-03-18 Auranofin: Repurposing an Old Drug for a Golden New Age Roder, Christine Thomson, Melanie J. Drugs R D Leading Article Drug discovery, development and registration is an expensive and time-consuming process associated with a high failure rate [Pessetto et al. (Mol Cancer Ther 12:1299–1309, 2013), Woodcock and Woosley (Annu Rev Med 59:1–12, 2008)]. Drug ‘repurposing’ is the identification of new therapeutic purposes for already approved drugs and is more affordable and achievable than novel drug discovery [Pessetto et al. (Mol Cancer Ther 12:1299–1309, 2013)]. Auranofin is a drug that is approved for the treatment of rheumatoid arthritis but is being investigated for potential therapeutic application in a number of other diseases including cancer, neurodegenerative disorders, HIV/AIDS, parasitic infections and bacterial infections [Tejman-Yarden et al. (Antimicrob Agents Chemother 57:2029–2035, 2013)]. The main mechanism of action of auranofin is through the inhibition of reduction/oxidation (redox) enzymes that are essential for maintaining intracellular levels of reactive oxygen species. Inhibition of these enzymes leads to cellular oxidative stress and intrinsic apoptosis [Pessetto et al. (Mol Cancer Ther 12:1299–1309, 2013), Fan et al. (Cell Death Dis 5:e1191, 2014), Fiskus et al. (Cancer Res 74:2520–2532, 2014), Marzano et al. (Free Radic Biol Med 42:872–881, 2007)]. Drugs such as auranofin that have already been approved for human use [Tejman-Yarden et al. (Antimicrob Agents Chemother 57:2029–2035, 2013)] can be brought into clinical use for other diseases relatively quickly and for a fraction of the cost of new drugs. Springer International Publishing 2015-02-20 2015-03 /pmc/articles/PMC4359176/ /pubmed/25698589 http://dx.doi.org/10.1007/s40268-015-0083-y Text en © The Author(s) 2015 https://creativecommons.org/licenses/by-nc/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Leading Article Roder, Christine Thomson, Melanie J. Auranofin: Repurposing an Old Drug for a Golden New Age |
title | Auranofin: Repurposing an Old Drug for a Golden New Age |
title_full | Auranofin: Repurposing an Old Drug for a Golden New Age |
title_fullStr | Auranofin: Repurposing an Old Drug for a Golden New Age |
title_full_unstemmed | Auranofin: Repurposing an Old Drug for a Golden New Age |
title_short | Auranofin: Repurposing an Old Drug for a Golden New Age |
title_sort | auranofin: repurposing an old drug for a golden new age |
topic | Leading Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359176/ https://www.ncbi.nlm.nih.gov/pubmed/25698589 http://dx.doi.org/10.1007/s40268-015-0083-y |
work_keys_str_mv | AT roderchristine auranofinrepurposinganolddrugforagoldennewage AT thomsonmelaniej auranofinrepurposinganolddrugforagoldennewage |