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Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity
Approved drugs target approximately 400 different mechanisms of action, of which as few as 60 are currently used as anti-cancer therapies. Given that on average it takes 10–15 years for a new cancer therapeutic to be approved, and the recent success of drug repurposing for agents such as thalidomide...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122340/ https://www.ncbi.nlm.nih.gov/pubmed/25093583 http://dx.doi.org/10.1371/journal.pone.0101708 |
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author | Roix, Jeffrey J. Harrison, S. D. Rainbolt, Elizabeth A. Meshaw, Kathryn R. McMurry, Avery S. Cheung, Peter Saha, Saurabh |
author_facet | Roix, Jeffrey J. Harrison, S. D. Rainbolt, Elizabeth A. Meshaw, Kathryn R. McMurry, Avery S. Cheung, Peter Saha, Saurabh |
author_sort | Roix, Jeffrey J. |
collection | PubMed |
description | Approved drugs target approximately 400 different mechanisms of action, of which as few as 60 are currently used as anti-cancer therapies. Given that on average it takes 10–15 years for a new cancer therapeutic to be approved, and the recent success of drug repurposing for agents such as thalidomide, we hypothesized that effective, safe cancer treatments may be found by testing approved drugs in new therapeutic settings. Here, we report in-vivo testing of a broad compound collection in cancer xenograft models. Using 182 compounds that target 125 unique target mechanisms, we identified 3 drugs that displayed reproducible activity in combination with the chemotherapeutic temozolomide. Candidate drugs appear effective at dose equivalents that exceed current prescription levels, suggesting that additional pre-clinical efforts will be needed before these drugs can be tested for efficacy in clinical trials. In total, we suggest drug repurposing is a relatively resource-intensive method that can identify approved medicines with a narrow margin of anti-cancer activity. |
format | Online Article Text |
id | pubmed-4122340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41223402014-08-12 Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity Roix, Jeffrey J. Harrison, S. D. Rainbolt, Elizabeth A. Meshaw, Kathryn R. McMurry, Avery S. Cheung, Peter Saha, Saurabh PLoS One Research Article Approved drugs target approximately 400 different mechanisms of action, of which as few as 60 are currently used as anti-cancer therapies. Given that on average it takes 10–15 years for a new cancer therapeutic to be approved, and the recent success of drug repurposing for agents such as thalidomide, we hypothesized that effective, safe cancer treatments may be found by testing approved drugs in new therapeutic settings. Here, we report in-vivo testing of a broad compound collection in cancer xenograft models. Using 182 compounds that target 125 unique target mechanisms, we identified 3 drugs that displayed reproducible activity in combination with the chemotherapeutic temozolomide. Candidate drugs appear effective at dose equivalents that exceed current prescription levels, suggesting that additional pre-clinical efforts will be needed before these drugs can be tested for efficacy in clinical trials. In total, we suggest drug repurposing is a relatively resource-intensive method that can identify approved medicines with a narrow margin of anti-cancer activity. Public Library of Science 2014-08-05 /pmc/articles/PMC4122340/ /pubmed/25093583 http://dx.doi.org/10.1371/journal.pone.0101708 Text en © 2014 Roix 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Roix, Jeffrey J. Harrison, S. D. Rainbolt, Elizabeth A. Meshaw, Kathryn R. McMurry, Avery S. Cheung, Peter Saha, Saurabh Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity |
title | Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity |
title_full | Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity |
title_fullStr | Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity |
title_full_unstemmed | Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity |
title_short | Systematic Repurposing Screening in Xenograft Models Identifies Approved Drugs with Novel Anti-Cancer Activity |
title_sort | systematic repurposing screening in xenograft models identifies approved drugs with novel anti-cancer activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122340/ https://www.ncbi.nlm.nih.gov/pubmed/25093583 http://dx.doi.org/10.1371/journal.pone.0101708 |
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