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Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer

Elucidation of tumour suppression mechanisms is a major challenge in cancer biology. Therefore, Peto's paradox, or low cancer incidence in large animals, has attracted focus. According to the gene-abundance hypothesis, which considers the increase/decrease in cancer-related genes with body size...

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Autores principales: Takemoto, Kazuhiro, Ii, Masato, Nishizuka, Satoshi S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043308/
https://www.ncbi.nlm.nih.gov/pubmed/27703689
http://dx.doi.org/10.1098/rsos.160267
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author Takemoto, Kazuhiro
Ii, Masato
Nishizuka, Satoshi S.
author_facet Takemoto, Kazuhiro
Ii, Masato
Nishizuka, Satoshi S.
author_sort Takemoto, Kazuhiro
collection PubMed
description Elucidation of tumour suppression mechanisms is a major challenge in cancer biology. Therefore, Peto's paradox, or low cancer incidence in large animals, has attracted focus. According to the gene-abundance hypothesis, which considers the increase/decrease in cancer-related genes with body size, researchers evaluated the associations between gene abundance and body size. However, previous studies only focused on a few specific gene functions and have ignored the alternative hypothesis (metabolic rate hypothesis): in this hypothesis, the cellular metabolic rate and subsequent oxidative stress decreases with increasing body size. In this study, we have elected to explore the gene-abundance hypothesis taking into account the metabolic rate hypothesis. Thus, we comprehensively investigated the correlation between the number of genes in various functional categories and body size while at the same time correcting for the mass-specific metabolic rate (B(c)). A number of gene functions that correlated with body size were initially identified, but they were found to be artefactual due to the decrease in B(c) with increasing body size. By contrast, immune system-related genes were found to increase with increasing body size when the correlation included this correction for B(c). These findings support the gene-abundance hypothesis and emphasize the importance of also taking into account the metabolic rate when evaluating gene abundance–body size relationships. This finding may be useful for understanding cancer evolution and tumour suppression mechanisms as well as for determining cancer-related genes and functions.
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spelling pubmed-50433082016-10-04 Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer Takemoto, Kazuhiro Ii, Masato Nishizuka, Satoshi S. R Soc Open Sci Cellular and Molecular Biology Elucidation of tumour suppression mechanisms is a major challenge in cancer biology. Therefore, Peto's paradox, or low cancer incidence in large animals, has attracted focus. According to the gene-abundance hypothesis, which considers the increase/decrease in cancer-related genes with body size, researchers evaluated the associations between gene abundance and body size. However, previous studies only focused on a few specific gene functions and have ignored the alternative hypothesis (metabolic rate hypothesis): in this hypothesis, the cellular metabolic rate and subsequent oxidative stress decreases with increasing body size. In this study, we have elected to explore the gene-abundance hypothesis taking into account the metabolic rate hypothesis. Thus, we comprehensively investigated the correlation between the number of genes in various functional categories and body size while at the same time correcting for the mass-specific metabolic rate (B(c)). A number of gene functions that correlated with body size were initially identified, but they were found to be artefactual due to the decrease in B(c) with increasing body size. By contrast, immune system-related genes were found to increase with increasing body size when the correlation included this correction for B(c). These findings support the gene-abundance hypothesis and emphasize the importance of also taking into account the metabolic rate when evaluating gene abundance–body size relationships. This finding may be useful for understanding cancer evolution and tumour suppression mechanisms as well as for determining cancer-related genes and functions. The Royal Society 2016-09-07 /pmc/articles/PMC5043308/ /pubmed/27703689 http://dx.doi.org/10.1098/rsos.160267 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Cellular and Molecular Biology
Takemoto, Kazuhiro
Ii, Masato
Nishizuka, Satoshi S.
Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer
title Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer
title_full Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer
title_fullStr Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer
title_full_unstemmed Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer
title_short Importance of metabolic rate to the relationship between the number of genes in a functional category and body size in Peto's paradox for cancer
title_sort importance of metabolic rate to the relationship between the number of genes in a functional category and body size in peto's paradox for cancer
topic Cellular and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043308/
https://www.ncbi.nlm.nih.gov/pubmed/27703689
http://dx.doi.org/10.1098/rsos.160267
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