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Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent

Cimetidine, the first H(2) receptor antagonist in widespread clinical use, has anti-cancer properties that have been elucidated in a broad range of pre-clinical and clinical studies for a number of different cancer types. These data are summarised and discussed in relation to a number of distinct me...

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Autores principales: Pantziarka, Pan, Bouche, Gauthier, Meheus, Lydie, Sukhatme, Vidula, Sukhatme, Vikas P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268104/
https://www.ncbi.nlm.nih.gov/pubmed/25525463
http://dx.doi.org/10.3332/ecancer.2014.485
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author Pantziarka, Pan
Bouche, Gauthier
Meheus, Lydie
Sukhatme, Vidula
Sukhatme, Vikas P
author_facet Pantziarka, Pan
Bouche, Gauthier
Meheus, Lydie
Sukhatme, Vidula
Sukhatme, Vikas P
author_sort Pantziarka, Pan
collection PubMed
description Cimetidine, the first H(2) receptor antagonist in widespread clinical use, has anti-cancer properties that have been elucidated in a broad range of pre-clinical and clinical studies for a number of different cancer types. These data are summarised and discussed in relation to a number of distinct mechanisms of action. Based on the evidence presented, it is proposed that cimetidine would synergise with a range of other drugs, including existing chemotherapeutics, and that further exploration of the potential of cimetidine as an anti-cancer therapeutic is warranted. Furthermore, there is compelling evidence that cimetidine administration during the peri-operative period may provide a survival benefit in some cancers. A number of possible combinations with other drugs are discussed in the supplementary material accompanying this paper.
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spelling pubmed-42681042014-12-18 Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent Pantziarka, Pan Bouche, Gauthier Meheus, Lydie Sukhatme, Vidula Sukhatme, Vikas P Ecancermedicalscience Clinical Study Cimetidine, the first H(2) receptor antagonist in widespread clinical use, has anti-cancer properties that have been elucidated in a broad range of pre-clinical and clinical studies for a number of different cancer types. These data are summarised and discussed in relation to a number of distinct mechanisms of action. Based on the evidence presented, it is proposed that cimetidine would synergise with a range of other drugs, including existing chemotherapeutics, and that further exploration of the potential of cimetidine as an anti-cancer therapeutic is warranted. Furthermore, there is compelling evidence that cimetidine administration during the peri-operative period may provide a survival benefit in some cancers. A number of possible combinations with other drugs are discussed in the supplementary material accompanying this paper. Cancer Intelligence 2014-11-26 /pmc/articles/PMC4268104/ /pubmed/25525463 http://dx.doi.org/10.3332/ecancer.2014.485 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution 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 Clinical Study
Pantziarka, Pan
Bouche, Gauthier
Meheus, Lydie
Sukhatme, Vidula
Sukhatme, Vikas P
Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent
title Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent
title_full Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent
title_fullStr Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent
title_full_unstemmed Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent
title_short Repurposing drugs in oncology (ReDO)—cimetidine as an anti-cancer agent
title_sort repurposing drugs in oncology (redo)—cimetidine as an anti-cancer agent
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268104/
https://www.ncbi.nlm.nih.gov/pubmed/25525463
http://dx.doi.org/10.3332/ecancer.2014.485
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