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Potential contribution of aspirin to cancer control programmes

Chemoprevention describes the potential of chemicals to intervene and block multi-stage carcinogenesis. Aspirin (acetylsalicylate) is showing cancer chemopreventive potential and the medicine has public health potential given that low doses also reduce the risk of cardiovascular events by up to 30%....

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Autor principal: Morgan, G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234056/
https://www.ncbi.nlm.nih.gov/pubmed/22275980
http://dx.doi.org/10.3332/ecancer.2008.100
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author Morgan, G
author_facet Morgan, G
author_sort Morgan, G
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description Chemoprevention describes the potential of chemicals to intervene and block multi-stage carcinogenesis. Aspirin (acetylsalicylate) is showing cancer chemopreventive potential and the medicine has public health potential given that low doses also reduce the risk of cardiovascular events by up to 30%. Whilst recognizing that aspirin has undesirable effects, such as increasing the risk of stomach bleeding, perhaps the medicine may compliment other cancer control programmes such as screening and lifestyle measures. Furthermore, perhaps the cancer chemopreventive potential of aspirin might be mediated, at least in part, by salicylate, which is present in fruits and vegetables. Salicylate might, therefore, be considered to be a nutraceutical. Furthermore, there are a number of matters that arise including the potential for the public health field to further advocate the self-care preventive agenda, which might include aspirin. Perhaps, it is now timely for a conference on the public health potential of aspirin to be convened.
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spelling pubmed-32340562012-01-24 Potential contribution of aspirin to cancer control programmes Morgan, G Ecancermedicalscience Policy Documents Chemoprevention describes the potential of chemicals to intervene and block multi-stage carcinogenesis. Aspirin (acetylsalicylate) is showing cancer chemopreventive potential and the medicine has public health potential given that low doses also reduce the risk of cardiovascular events by up to 30%. Whilst recognizing that aspirin has undesirable effects, such as increasing the risk of stomach bleeding, perhaps the medicine may compliment other cancer control programmes such as screening and lifestyle measures. Furthermore, perhaps the cancer chemopreventive potential of aspirin might be mediated, at least in part, by salicylate, which is present in fruits and vegetables. Salicylate might, therefore, be considered to be a nutraceutical. Furthermore, there are a number of matters that arise including the potential for the public health field to further advocate the self-care preventive agenda, which might include aspirin. Perhaps, it is now timely for a conference on the public health potential of aspirin to be convened. Cancer Intelligence 2008-11-12 /pmc/articles/PMC3234056/ /pubmed/22275980 http://dx.doi.org/10.3332/ecancer.2008.100 Text en Copyright: © the authors; licensee ecancermedicalscience. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Policy Documents
Morgan, G
Potential contribution of aspirin to cancer control programmes
title Potential contribution of aspirin to cancer control programmes
title_full Potential contribution of aspirin to cancer control programmes
title_fullStr Potential contribution of aspirin to cancer control programmes
title_full_unstemmed Potential contribution of aspirin to cancer control programmes
title_short Potential contribution of aspirin to cancer control programmes
title_sort potential contribution of aspirin to cancer control programmes
topic Policy Documents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234056/
https://www.ncbi.nlm.nih.gov/pubmed/22275980
http://dx.doi.org/10.3332/ecancer.2008.100
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