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Tumor Acidity as Evolutionary Spite
Most cancer cells shift their metabolic pathway from a metabolism reflecting the Pasteur-effect into one reflecting the Warburg-effect. This shift creates an acidic microenvironment around the tumor and becomes the driving force for a positive carcinogenesis feedback loop. As a consequence of tumor...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756368/ https://www.ncbi.nlm.nih.gov/pubmed/24310355 http://dx.doi.org/10.3390/cancers3010408 |
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author | Alfarouk, Khalid O. Muddathir, Abdel Khalig Shayoub, Mohammed E. A. |
author_facet | Alfarouk, Khalid O. Muddathir, Abdel Khalig Shayoub, Mohammed E. A. |
author_sort | Alfarouk, Khalid O. |
collection | PubMed |
description | Most cancer cells shift their metabolic pathway from a metabolism reflecting the Pasteur-effect into one reflecting the Warburg-effect. This shift creates an acidic microenvironment around the tumor and becomes the driving force for a positive carcinogenesis feedback loop. As a consequence of tumor acidity, the tumor microenvironment encourages a selection of certain cell phenotypes that are able to survive in this caustic environment to the detriment of other cell types. This selection can be described by a process which can be modeled upon spite: the tumor cells reduce their own fitness by making an acidic environment, but this reduces the fitness of their competitors to an even greater extent. Moreover, the environment is an important dimension that further drives this spite process. Thus, diminishing the selective environment most probably interferes with the spite process. Such interference has been recently utilized in cancer treatment. |
format | Online Article Text |
id | pubmed-3756368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-37563682013-09-04 Tumor Acidity as Evolutionary Spite Alfarouk, Khalid O. Muddathir, Abdel Khalig Shayoub, Mohammed E. A. Cancers (Basel) Opinion Most cancer cells shift their metabolic pathway from a metabolism reflecting the Pasteur-effect into one reflecting the Warburg-effect. This shift creates an acidic microenvironment around the tumor and becomes the driving force for a positive carcinogenesis feedback loop. As a consequence of tumor acidity, the tumor microenvironment encourages a selection of certain cell phenotypes that are able to survive in this caustic environment to the detriment of other cell types. This selection can be described by a process which can be modeled upon spite: the tumor cells reduce their own fitness by making an acidic environment, but this reduces the fitness of their competitors to an even greater extent. Moreover, the environment is an important dimension that further drives this spite process. Thus, diminishing the selective environment most probably interferes with the spite process. Such interference has been recently utilized in cancer treatment. Molecular Diversity Preservation International (MDPI) 2011-01-20 /pmc/articles/PMC3756368/ /pubmed/24310355 http://dx.doi.org/10.3390/cancers3010408 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Opinion Alfarouk, Khalid O. Muddathir, Abdel Khalig Shayoub, Mohammed E. A. Tumor Acidity as Evolutionary Spite |
title | Tumor Acidity as Evolutionary Spite |
title_full | Tumor Acidity as Evolutionary Spite |
title_fullStr | Tumor Acidity as Evolutionary Spite |
title_full_unstemmed | Tumor Acidity as Evolutionary Spite |
title_short | Tumor Acidity as Evolutionary Spite |
title_sort | tumor acidity as evolutionary spite |
topic | Opinion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756368/ https://www.ncbi.nlm.nih.gov/pubmed/24310355 http://dx.doi.org/10.3390/cancers3010408 |
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