Cargando…

Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites

Background: Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death in the world. Nanosecond pulsed electric fields (nsPEFs) have emerged as a new treatment for cancer. This study aims to identify the effectiveness of nsPEFs in the treatment of HCC and analyze the alteratio...

Descripción completa

Detalles Bibliográficos
Autores principales: Zou, Yawen, Sun, Ying, Chen, Xinhua, Hong, Liangjie, Dong, Gang, Bai, Xiwen, Wang, Haiyu, Rao, Benchen, Ren, Zhigang, Yu, Zujiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205996/
https://www.ncbi.nlm.nih.gov/pubmed/37234705
http://dx.doi.org/10.3389/fphar.2023.1163628
_version_ 1785046130489294848
author Zou, Yawen
Sun, Ying
Chen, Xinhua
Hong, Liangjie
Dong, Gang
Bai, Xiwen
Wang, Haiyu
Rao, Benchen
Ren, Zhigang
Yu, Zujiang
author_facet Zou, Yawen
Sun, Ying
Chen, Xinhua
Hong, Liangjie
Dong, Gang
Bai, Xiwen
Wang, Haiyu
Rao, Benchen
Ren, Zhigang
Yu, Zujiang
author_sort Zou, Yawen
collection PubMed
description Background: Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death in the world. Nanosecond pulsed electric fields (nsPEFs) have emerged as a new treatment for cancer. This study aims to identify the effectiveness of nsPEFs in the treatment of HCC and analyze the alterations in the gut microbiome and serum metabonomics after ablation. Methods: C57BL/6 mice were randomly divided into three groups: healthy control mice (n = 10), HCC mice (n = 10), and nsPEF-treated HCC mice (n = 23). Hep1-6 cell lines were used to establish the HCC model in situ. Histopathological staining was performed on tumor tissues. The gut microbiome was analyzed by 16S rRNA sequencing. Serum metabolites were analyzed by liquid chromatography–mass spectrometry (LC-MS) metabolomic analysis. Spearman’s correlation analysis was carried out to analyze the correlation between the gut microbiome and serum metabonomics. Results: The fluorescence image showed that nsPEFs were significantly effective. Histopathological staining identified nuclear pyknosis and cell necrosis in the nsPEF group. The expression of CD34, PCNA, and VEGF decreased significantly in the nsPEF group. Compared with normal mice, the gut microbiome diversity of HCC mice was increased. Eight genera including Alistipes and Muribaculaceae were enriched in the HCC group. Inversely, these genera decreased in the nsPEF group. LC-MS analysis confirmed that there were significant differences in serum metabolism among the three groups. Correlation analysis showed crucial relationships between the gut microbiome and serum metabolites that are involved in nsPEF ablation of HCC. Conclusion: As a new minimally invasive treatment for tumor ablation, nsPEFs have an excellent ablation effect. The alterations in the gut microbiome and serum metabolites may participate in the prognosis of HCC ablation.
format Online
Article
Text
id pubmed-10205996
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-102059962023-05-25 Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites Zou, Yawen Sun, Ying Chen, Xinhua Hong, Liangjie Dong, Gang Bai, Xiwen Wang, Haiyu Rao, Benchen Ren, Zhigang Yu, Zujiang Front Pharmacol Pharmacology Background: Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death in the world. Nanosecond pulsed electric fields (nsPEFs) have emerged as a new treatment for cancer. This study aims to identify the effectiveness of nsPEFs in the treatment of HCC and analyze the alterations in the gut microbiome and serum metabonomics after ablation. Methods: C57BL/6 mice were randomly divided into three groups: healthy control mice (n = 10), HCC mice (n = 10), and nsPEF-treated HCC mice (n = 23). Hep1-6 cell lines were used to establish the HCC model in situ. Histopathological staining was performed on tumor tissues. The gut microbiome was analyzed by 16S rRNA sequencing. Serum metabolites were analyzed by liquid chromatography–mass spectrometry (LC-MS) metabolomic analysis. Spearman’s correlation analysis was carried out to analyze the correlation between the gut microbiome and serum metabonomics. Results: The fluorescence image showed that nsPEFs were significantly effective. Histopathological staining identified nuclear pyknosis and cell necrosis in the nsPEF group. The expression of CD34, PCNA, and VEGF decreased significantly in the nsPEF group. Compared with normal mice, the gut microbiome diversity of HCC mice was increased. Eight genera including Alistipes and Muribaculaceae were enriched in the HCC group. Inversely, these genera decreased in the nsPEF group. LC-MS analysis confirmed that there were significant differences in serum metabolism among the three groups. Correlation analysis showed crucial relationships between the gut microbiome and serum metabolites that are involved in nsPEF ablation of HCC. Conclusion: As a new minimally invasive treatment for tumor ablation, nsPEFs have an excellent ablation effect. The alterations in the gut microbiome and serum metabolites may participate in the prognosis of HCC ablation. Frontiers Media S.A. 2023-05-10 /pmc/articles/PMC10205996/ /pubmed/37234705 http://dx.doi.org/10.3389/fphar.2023.1163628 Text en Copyright © 2023 Zou, Sun, Chen, Hong, Dong, Bai, Wang, Rao, Ren and Yu. 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 Pharmacology
Zou, Yawen
Sun, Ying
Chen, Xinhua
Hong, Liangjie
Dong, Gang
Bai, Xiwen
Wang, Haiyu
Rao, Benchen
Ren, Zhigang
Yu, Zujiang
Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites
title Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites
title_full Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites
title_fullStr Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites
title_full_unstemmed Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites
title_short Nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites
title_sort nanosecond pulse effectively ablated hepatocellular carcinoma with alterations in the gut microbiome and serum metabolites
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205996/
https://www.ncbi.nlm.nih.gov/pubmed/37234705
http://dx.doi.org/10.3389/fphar.2023.1163628
work_keys_str_mv AT zouyawen nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT sunying nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT chenxinhua nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT hongliangjie nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT donggang nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT baixiwen nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT wanghaiyu nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT raobenchen nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT renzhigang nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites
AT yuzujiang nanosecondpulseeffectivelyablatedhepatocellularcarcinomawithalterationsinthegutmicrobiomeandserummetabolites