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Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice

The homeostasis of the gut microbiota and circadian rhythm is critical to host health, and both are inextricably intertwined with lung cancer. Although time-restricted feeding (TRF) can maintain circadian synchronization and improve metabolic disorders, the effects of TRF on the fecal microbiome, me...

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Autores principales: Fang, Gaofeng, Wang, Shengquan, Chen, Qianyao, Luo, Han, Lian, Xuemei, Shi, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590998/
https://www.ncbi.nlm.nih.gov/pubmed/37852131
http://dx.doi.org/10.1016/j.neo.2023.100943
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author Fang, Gaofeng
Wang, Shengquan
Chen, Qianyao
Luo, Han
Lian, Xuemei
Shi, Dan
author_facet Fang, Gaofeng
Wang, Shengquan
Chen, Qianyao
Luo, Han
Lian, Xuemei
Shi, Dan
author_sort Fang, Gaofeng
collection PubMed
description The homeostasis of the gut microbiota and circadian rhythm is critical to host health, and both are inextricably intertwined with lung cancer. Although time-restricted feeding (TRF) can maintain circadian synchronization and improve metabolic disorders, the effects of TRF on the fecal microbiome, metabolome and their diurnal oscillations in lung cancer have not been discussed. We performed 16S rRNA sequencing and untargeted metabonomic sequencing of the feces prepared from models of tumor-bearing BALB/c nude mice and urethane-induced lung cancer. We demonstrated for the first time that TRF significantly delayed the growth of lung tumors. Moreover, TRF altered the abundances of the fecal microbiome, metabolome and circadian clocks, as well as their rhythmicity, in lung cancer models of tumor-bearing BALB/c nude mice and/or urethane-induced lung cancer C57BL/6J mice. The results of fecal microbiota transplantation proved that the antitumor effects of TRF occur by regulating the fecal microbiota. Notably, Lactobacillus and Bacillus were increased upon TRF and were correlated with most differential metabolites. Pathway enrichment analysis of metabolites revealed that TRF mainly affected immune and inflammatory processes, which might further explain how TRF exerted its anticancer benefits. These findings underscore the possibility that the fecal microbiome/metabolome regulates lung cancer following a TRF paradigm.
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spelling pubmed-105909982023-10-24 Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice Fang, Gaofeng Wang, Shengquan Chen, Qianyao Luo, Han Lian, Xuemei Shi, Dan Neoplasia Original Research The homeostasis of the gut microbiota and circadian rhythm is critical to host health, and both are inextricably intertwined with lung cancer. Although time-restricted feeding (TRF) can maintain circadian synchronization and improve metabolic disorders, the effects of TRF on the fecal microbiome, metabolome and their diurnal oscillations in lung cancer have not been discussed. We performed 16S rRNA sequencing and untargeted metabonomic sequencing of the feces prepared from models of tumor-bearing BALB/c nude mice and urethane-induced lung cancer. We demonstrated for the first time that TRF significantly delayed the growth of lung tumors. Moreover, TRF altered the abundances of the fecal microbiome, metabolome and circadian clocks, as well as their rhythmicity, in lung cancer models of tumor-bearing BALB/c nude mice and/or urethane-induced lung cancer C57BL/6J mice. The results of fecal microbiota transplantation proved that the antitumor effects of TRF occur by regulating the fecal microbiota. Notably, Lactobacillus and Bacillus were increased upon TRF and were correlated with most differential metabolites. Pathway enrichment analysis of metabolites revealed that TRF mainly affected immune and inflammatory processes, which might further explain how TRF exerted its anticancer benefits. These findings underscore the possibility that the fecal microbiome/metabolome regulates lung cancer following a TRF paradigm. Neoplasia Press 2023-10-16 /pmc/articles/PMC10590998/ /pubmed/37852131 http://dx.doi.org/10.1016/j.neo.2023.100943 Text en © 2023 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Fang, Gaofeng
Wang, Shengquan
Chen, Qianyao
Luo, Han
Lian, Xuemei
Shi, Dan
Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice
title Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice
title_full Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice
title_fullStr Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice
title_full_unstemmed Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice
title_short Time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice
title_sort time-restricted feeding affects the fecal microbiome metabolome and its diurnal oscillations in lung cancer mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590998/
https://www.ncbi.nlm.nih.gov/pubmed/37852131
http://dx.doi.org/10.1016/j.neo.2023.100943
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