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Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota

Imbalances in intestinal bacteria correlate with colitis-associated colorectal cancer (CAC). Traditional Chinese medicines have been used to adjust the gut microbiota, and isoliquiritigenin (ISL), a flavonoid extracted from licorice, has shown antitumor efficacy. In this study, the effects of ISL on...

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Autores principales: Wu, Minna, Wu, Yaqi, Deng, Baoguo, Li, Jinsong, Cao, Haiying, Qu, Yan, Qian, Xinlai, Zhong, Genshen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356739/
https://www.ncbi.nlm.nih.gov/pubmed/27863401
http://dx.doi.org/10.18632/oncotarget.13347
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author Wu, Minna
Wu, Yaqi
Deng, Baoguo
Li, Jinsong
Cao, Haiying
Qu, Yan
Qian, Xinlai
Zhong, Genshen
author_facet Wu, Minna
Wu, Yaqi
Deng, Baoguo
Li, Jinsong
Cao, Haiying
Qu, Yan
Qian, Xinlai
Zhong, Genshen
author_sort Wu, Minna
collection PubMed
description Imbalances in intestinal bacteria correlate with colitis-associated colorectal cancer (CAC). Traditional Chinese medicines have been used to adjust the gut microbiota, and isoliquiritigenin (ISL), a flavonoid extracted from licorice, has shown antitumor efficacy. In this study, the effects of ISL on CAC development and the gut microbiota were evaluated using an azoxymethane and dextran sulphate sodium (AOM/DSS)-induced mouse model of CAC (CACM). Histopathological analysis suggested that ISL reduced tumor incidence in vivo. Moreover, high-throughput sequencing and terminal restriction fragment length polymorphism (T-RFLP) studies of the bacterial 16S rRNA gene revealed that the structure of the gut microbial community shifted significantly following AOM/DSS treatment, and that effect was alleviated by treatment with high-dose ISL (150 mg/kg). Compared to the microbiota in the control mice (CK), the levels of Bacteroidetes decreased and the levels of Firmicutes increased during CAC development. ISL reversed the imbalance at the phylum level and altered the familial constituents of the gut microbiota. Specifically, the abundance of Helicobacteraceae increased after treatment with high-dose ISL, while the abundance of Lachnospiraceae and Rikenellaceae decreased. At the genus level, ISL reduced the abundance of opportunistic pathogens (Escherichia and Enterococcus), and increased the levels of probiotics, particularly butyrate-producing bacteria (Butyricicoccus, Clostridium, and Ruminococcus). Thus, ISL protects mice from AOM/DSS-induced CAC, and ISL and the gut microbiota may have synergistic anti-cancer effects.
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spelling pubmed-53567392017-04-26 Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota Wu, Minna Wu, Yaqi Deng, Baoguo Li, Jinsong Cao, Haiying Qu, Yan Qian, Xinlai Zhong, Genshen Oncotarget Research Paper Imbalances in intestinal bacteria correlate with colitis-associated colorectal cancer (CAC). Traditional Chinese medicines have been used to adjust the gut microbiota, and isoliquiritigenin (ISL), a flavonoid extracted from licorice, has shown antitumor efficacy. In this study, the effects of ISL on CAC development and the gut microbiota were evaluated using an azoxymethane and dextran sulphate sodium (AOM/DSS)-induced mouse model of CAC (CACM). Histopathological analysis suggested that ISL reduced tumor incidence in vivo. Moreover, high-throughput sequencing and terminal restriction fragment length polymorphism (T-RFLP) studies of the bacterial 16S rRNA gene revealed that the structure of the gut microbial community shifted significantly following AOM/DSS treatment, and that effect was alleviated by treatment with high-dose ISL (150 mg/kg). Compared to the microbiota in the control mice (CK), the levels of Bacteroidetes decreased and the levels of Firmicutes increased during CAC development. ISL reversed the imbalance at the phylum level and altered the familial constituents of the gut microbiota. Specifically, the abundance of Helicobacteraceae increased after treatment with high-dose ISL, while the abundance of Lachnospiraceae and Rikenellaceae decreased. At the genus level, ISL reduced the abundance of opportunistic pathogens (Escherichia and Enterococcus), and increased the levels of probiotics, particularly butyrate-producing bacteria (Butyricicoccus, Clostridium, and Ruminococcus). Thus, ISL protects mice from AOM/DSS-induced CAC, and ISL and the gut microbiota may have synergistic anti-cancer effects. Impact Journals LLC 2016-11-15 /pmc/articles/PMC5356739/ /pubmed/27863401 http://dx.doi.org/10.18632/oncotarget.13347 Text en Copyright: © 2016 Wu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wu, Minna
Wu, Yaqi
Deng, Baoguo
Li, Jinsong
Cao, Haiying
Qu, Yan
Qian, Xinlai
Zhong, Genshen
Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota
title Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota
title_full Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota
title_fullStr Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota
title_full_unstemmed Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota
title_short Isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota
title_sort isoliquiritigenin decreases the incidence of colitis-associated colorectal cancer by modulating the intestinal microbiota
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356739/
https://www.ncbi.nlm.nih.gov/pubmed/27863401
http://dx.doi.org/10.18632/oncotarget.13347
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