Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues

Abstract Background Intratumoral microbial communities have been recently discovered to exist in a variety of cancers and have been found to be intricately involved in tumour progression. Therefore, investigating the profiles and functions of intratumoral microbial distribution in hepatocellular car...

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Main Authors: Yuting He, Qiyao Zhang, Xiao Yu, Shuijun Zhang, Wenzhi Guo
Format: Article
Language:English
Published: BMC 2023-02-01
Series:Journal of Translational Medicine
Subjects:
Online Access:https://doi.org/10.1186/s12967-023-03938-6
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author Yuting He
Qiyao Zhang
Xiao Yu
Shuijun Zhang
Wenzhi Guo
author_facet Yuting He
Qiyao Zhang
Xiao Yu
Shuijun Zhang
Wenzhi Guo
author_sort Yuting He
collection DOAJ
description Abstract Background Intratumoral microbial communities have been recently discovered to exist in a variety of cancers and have been found to be intricately involved in tumour progression. Therefore, investigating the profiles and functions of intratumoral microbial distribution in hepatocellular carcinoma (HCC) is imperative. Methods To verify the presence of microorganisms in HCC, we performed fluorescence in situ hybridization (FISH) using HCC tissues and conducted MiSeq using 99 HCC and paracancerous tissues to identify the key microorganisms and changes in metabolic pathways affecting HCC progression through a variety of bioinformatics methods. Results Microbial diversity was significantly higher in HCC tissues than in adjacent tissues. The abundances of microorganisms such as Enterobacteriaceae, Fusobacterium and Neisseria were significantly increased in HCC tissues, while the abundances of certain antitumour bacteria such as Pseudomonas were decreased. Processes such as fatty acid and lipid synthesis were significantly enhanced in the microbiota in HCC tissues, which may be a key factor through which intratumoral microbes influence tumour progression. There were considerable differences in the microbes and their functions within tumour tissue collected from patients with different clinical features. Conclusion We comprehensively evaluated the intratumoral microbial atlas of HCC tissue and preliminarily explored the mechanism of the effects of the microbial community involving changes in lipid metabolism and effects on HCC progression, which lays the foundation for further research in this field.
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spelling doaj.art-d97418ad5bec46e681b87ba8db633c262023-02-05T12:22:29ZengBMCJournal of Translational Medicine1479-58762023-02-0121111210.1186/s12967-023-03938-6Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissuesYuting He0Qiyao Zhang1Xiao Yu2Shuijun Zhang3Wenzhi Guo4Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou UniversityAbstract Background Intratumoral microbial communities have been recently discovered to exist in a variety of cancers and have been found to be intricately involved in tumour progression. Therefore, investigating the profiles and functions of intratumoral microbial distribution in hepatocellular carcinoma (HCC) is imperative. Methods To verify the presence of microorganisms in HCC, we performed fluorescence in situ hybridization (FISH) using HCC tissues and conducted MiSeq using 99 HCC and paracancerous tissues to identify the key microorganisms and changes in metabolic pathways affecting HCC progression through a variety of bioinformatics methods. Results Microbial diversity was significantly higher in HCC tissues than in adjacent tissues. The abundances of microorganisms such as Enterobacteriaceae, Fusobacterium and Neisseria were significantly increased in HCC tissues, while the abundances of certain antitumour bacteria such as Pseudomonas were decreased. Processes such as fatty acid and lipid synthesis were significantly enhanced in the microbiota in HCC tissues, which may be a key factor through which intratumoral microbes influence tumour progression. There were considerable differences in the microbes and their functions within tumour tissue collected from patients with different clinical features. Conclusion We comprehensively evaluated the intratumoral microbial atlas of HCC tissue and preliminarily explored the mechanism of the effects of the microbial community involving changes in lipid metabolism and effects on HCC progression, which lays the foundation for further research in this field.https://doi.org/10.1186/s12967-023-03938-6Hepatocellular carcinomaIntratumoral microbiotaMetabolic pathwayFatty acid and lipid synthesisMiSeq
spellingShingle Yuting He
Qiyao Zhang
Xiao Yu
Shuijun Zhang
Wenzhi Guo
Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues
Journal of Translational Medicine
Hepatocellular carcinoma
Intratumoral microbiota
Metabolic pathway
Fatty acid and lipid synthesis
MiSeq
title Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues
title_full Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues
title_fullStr Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues
title_full_unstemmed Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues
title_short Overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues
title_sort overview of microbial profiles in human hepatocellular carcinoma and adjacent nontumor tissues
topic Hepatocellular carcinoma
Intratumoral microbiota
Metabolic pathway
Fatty acid and lipid synthesis
MiSeq
url https://doi.org/10.1186/s12967-023-03938-6
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