Cargando…

Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment

BACKGROUND AND AIMS: Intestinal flora is closely associated with the occurrence and development of hepatocellular carcinoma (HCC). However, gut microbial changes and biological mechanisms in HCC after transarterial chemoembolization (TACE) treatment are rarely reported. METHODS: We evaluated changes...

Descripción completa

Detalles Bibliográficos
Autores principales: Bian, Chao-fan, Wang, Ying, Yu, Ao, Fu, Lulan, Zhang, Ding, Zhu, Wenzhi, Lv, Weifu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577458/
https://www.ncbi.nlm.nih.gov/pubmed/36267958
http://dx.doi.org/10.3389/fonc.2022.1002589
_version_ 1784811760060989440
author Bian, Chao-fan
Wang, Ying
Yu, Ao
Fu, Lulan
Zhang, Ding
Zhu, Wenzhi
Lv, Weifu
author_facet Bian, Chao-fan
Wang, Ying
Yu, Ao
Fu, Lulan
Zhang, Ding
Zhu, Wenzhi
Lv, Weifu
author_sort Bian, Chao-fan
collection PubMed
description BACKGROUND AND AIMS: Intestinal flora is closely associated with the occurrence and development of hepatocellular carcinoma (HCC). However, gut microbial changes and biological mechanisms in HCC after transarterial chemoembolization (TACE) treatment are rarely reported. METHODS: We evaluated changes in intestinal flora after TACE in rabbit HCC models and assessed the impact of these changes on the disease. Twenty-four rabbit VX2 HCC models were established and intestinal flora structures, intestinal barrier function, changes in blood lipopolysaccharide (LPS) levels, Toll-like receptor 4 (TLR4), Cyclooxygenase-2 (COX-2), and p-signal transducer and activator of transcription 3(p-STAT3) protein expression levels were studied after TACE treatment. RESULTS: Compared with healthy rabbits, the intestinal flora in HCC models exhibited structural changes; intestinal barrier function was decreased, and increased LPS levels entered the circulation. A short-term follow-up after TACE showed the procedure partially reversed the intestinal microflora disorder caused by the tumor: intestinal barrier and liver functions were improved, intestinal LPS levels in the blood were reduced, and liver metabolism toward LPS was enhanced. Correlation analyses of the first 75 significantly changed bacteria with clinical factors showed that harmful bacteria had decreased and beneficial bacteria increased. Blood LPS levels and downstream signaling molecule TLR4, COX-2, and p-STAT3 protein expression levels were reduced, which correlated with tumor drug resistance and invasion capabilities. CONCLUSIONS: We first characterized gut microbiota changes and biological mechanisms in HCC after TACE treatment. Our data provide a theoretical research basis for TACE combined with an intestinal flora intervention and systemic chemotherapy.
format Online
Article
Text
id pubmed-9577458
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-95774582022-10-19 Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment Bian, Chao-fan Wang, Ying Yu, Ao Fu, Lulan Zhang, Ding Zhu, Wenzhi Lv, Weifu Front Oncol Oncology BACKGROUND AND AIMS: Intestinal flora is closely associated with the occurrence and development of hepatocellular carcinoma (HCC). However, gut microbial changes and biological mechanisms in HCC after transarterial chemoembolization (TACE) treatment are rarely reported. METHODS: We evaluated changes in intestinal flora after TACE in rabbit HCC models and assessed the impact of these changes on the disease. Twenty-four rabbit VX2 HCC models were established and intestinal flora structures, intestinal barrier function, changes in blood lipopolysaccharide (LPS) levels, Toll-like receptor 4 (TLR4), Cyclooxygenase-2 (COX-2), and p-signal transducer and activator of transcription 3(p-STAT3) protein expression levels were studied after TACE treatment. RESULTS: Compared with healthy rabbits, the intestinal flora in HCC models exhibited structural changes; intestinal barrier function was decreased, and increased LPS levels entered the circulation. A short-term follow-up after TACE showed the procedure partially reversed the intestinal microflora disorder caused by the tumor: intestinal barrier and liver functions were improved, intestinal LPS levels in the blood were reduced, and liver metabolism toward LPS was enhanced. Correlation analyses of the first 75 significantly changed bacteria with clinical factors showed that harmful bacteria had decreased and beneficial bacteria increased. Blood LPS levels and downstream signaling molecule TLR4, COX-2, and p-STAT3 protein expression levels were reduced, which correlated with tumor drug resistance and invasion capabilities. CONCLUSIONS: We first characterized gut microbiota changes and biological mechanisms in HCC after TACE treatment. Our data provide a theoretical research basis for TACE combined with an intestinal flora intervention and systemic chemotherapy. Frontiers Media S.A. 2022-10-04 /pmc/articles/PMC9577458/ /pubmed/36267958 http://dx.doi.org/10.3389/fonc.2022.1002589 Text en Copyright © 2022 Bian, Wang, Yu, Fu, Zhang, Zhu and Lv https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Bian, Chao-fan
Wang, Ying
Yu, Ao
Fu, Lulan
Zhang, Ding
Zhu, Wenzhi
Lv, Weifu
Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment
title Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment
title_full Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment
title_fullStr Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment
title_full_unstemmed Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment
title_short Gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment
title_sort gut microbiota changes and biological mechanism in hepatocellular carcinoma after transarterial chemoembolization treatment
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577458/
https://www.ncbi.nlm.nih.gov/pubmed/36267958
http://dx.doi.org/10.3389/fonc.2022.1002589
work_keys_str_mv AT bianchaofan gutmicrobiotachangesandbiologicalmechanisminhepatocellularcarcinomaaftertransarterialchemoembolizationtreatment
AT wangying gutmicrobiotachangesandbiologicalmechanisminhepatocellularcarcinomaaftertransarterialchemoembolizationtreatment
AT yuao gutmicrobiotachangesandbiologicalmechanisminhepatocellularcarcinomaaftertransarterialchemoembolizationtreatment
AT fululan gutmicrobiotachangesandbiologicalmechanisminhepatocellularcarcinomaaftertransarterialchemoembolizationtreatment
AT zhangding gutmicrobiotachangesandbiologicalmechanisminhepatocellularcarcinomaaftertransarterialchemoembolizationtreatment
AT zhuwenzhi gutmicrobiotachangesandbiologicalmechanisminhepatocellularcarcinomaaftertransarterialchemoembolizationtreatment
AT lvweifu gutmicrobiotachangesandbiologicalmechanisminhepatocellularcarcinomaaftertransarterialchemoembolizationtreatment