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Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis

BACKGROUND: Currently ketogenic diets (KDs) are hyped as an anti-tumor intervention aimed at exploiting the metabolic abnormalities of cancer cells. However, while data in humans is sparse, translation of murine tumor models to the clinic is further hampered by small sample sizes, heterogeneous sett...

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Autores principales: Klement, Rainer J., Champ, Colin E., Otto, Christoph, Kämmerer, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861343/
https://www.ncbi.nlm.nih.gov/pubmed/27159218
http://dx.doi.org/10.1371/journal.pone.0155050
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author Klement, Rainer J.
Champ, Colin E.
Otto, Christoph
Kämmerer, Ulrike
author_facet Klement, Rainer J.
Champ, Colin E.
Otto, Christoph
Kämmerer, Ulrike
author_sort Klement, Rainer J.
collection PubMed
description BACKGROUND: Currently ketogenic diets (KDs) are hyped as an anti-tumor intervention aimed at exploiting the metabolic abnormalities of cancer cells. However, while data in humans is sparse, translation of murine tumor models to the clinic is further hampered by small sample sizes, heterogeneous settings and mixed results concerning tumor growth retardation. The aim was therefore to synthesize the evidence for a growth inhibiting effect of KDs when used as a monotherapy in mice. METHODS: We conducted a Bayesian random effects meta-analysis on all studies assessing the survival (defined as the time to reach a pre-defined endpoint such as tumor volume) of mice on an unrestricted KD compared to a high carbohydrate standard diet (SD). For 12 studies meeting the inclusion criteria either a mean survival time ratio (MR) or hazard ratio (HR) between the KD and SD groups could be obtained. The posterior estimates for the MR and HR averaged over four priors on the between-study heterogeneity τ(2) were MR = 0.85 (95% highest posterior density interval (HPDI) = [0.73, 0.97]) and HR = 0.55 (95% HPDI = [0.26, 0.87]), indicating a significant overall benefit of the KD in terms of prolonged mean survival times and reduced hazard rate. All studies that used a brain tumor model also chose a late starting point for the KD (at least one day after tumor initiation) which accounted for 26% of the heterogeneity. In this subgroup the KD was less effective (MR = 0.89, 95% HPDI = [0.76, 1.04]). CONCLUSIONS: There was an overall tumor growth delaying effect of unrestricted KDs in mice. Future experiments should aim at differentiating the effects of KD timing versus tumor location, since external evidence is currently consistent with an influence of both of these factors.
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spelling pubmed-48613432016-05-13 Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis Klement, Rainer J. Champ, Colin E. Otto, Christoph Kämmerer, Ulrike PLoS One Research Article BACKGROUND: Currently ketogenic diets (KDs) are hyped as an anti-tumor intervention aimed at exploiting the metabolic abnormalities of cancer cells. However, while data in humans is sparse, translation of murine tumor models to the clinic is further hampered by small sample sizes, heterogeneous settings and mixed results concerning tumor growth retardation. The aim was therefore to synthesize the evidence for a growth inhibiting effect of KDs when used as a monotherapy in mice. METHODS: We conducted a Bayesian random effects meta-analysis on all studies assessing the survival (defined as the time to reach a pre-defined endpoint such as tumor volume) of mice on an unrestricted KD compared to a high carbohydrate standard diet (SD). For 12 studies meeting the inclusion criteria either a mean survival time ratio (MR) or hazard ratio (HR) between the KD and SD groups could be obtained. The posterior estimates for the MR and HR averaged over four priors on the between-study heterogeneity τ(2) were MR = 0.85 (95% highest posterior density interval (HPDI) = [0.73, 0.97]) and HR = 0.55 (95% HPDI = [0.26, 0.87]), indicating a significant overall benefit of the KD in terms of prolonged mean survival times and reduced hazard rate. All studies that used a brain tumor model also chose a late starting point for the KD (at least one day after tumor initiation) which accounted for 26% of the heterogeneity. In this subgroup the KD was less effective (MR = 0.89, 95% HPDI = [0.76, 1.04]). CONCLUSIONS: There was an overall tumor growth delaying effect of unrestricted KDs in mice. Future experiments should aim at differentiating the effects of KD timing versus tumor location, since external evidence is currently consistent with an influence of both of these factors. Public Library of Science 2016-05-09 /pmc/articles/PMC4861343/ /pubmed/27159218 http://dx.doi.org/10.1371/journal.pone.0155050 Text en © 2016 Klement 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Klement, Rainer J.
Champ, Colin E.
Otto, Christoph
Kämmerer, Ulrike
Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis
title Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis
title_full Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis
title_fullStr Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis
title_full_unstemmed Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis
title_short Anti-Tumor Effects of Ketogenic Diets in Mice: A Meta-Analysis
title_sort anti-tumor effects of ketogenic diets in mice: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861343/
https://www.ncbi.nlm.nih.gov/pubmed/27159218
http://dx.doi.org/10.1371/journal.pone.0155050
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