Fusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma

Abstract Background Fusobacterium nucleatum (F. nucleatum) is a vital pro-oncogenic bacterium. Our previous study revealed that a high abundance of F. nucleatum in head and neck squamous cell carcinoma (HNSCC) is correlated with poor patient prognosis. However, the impact of F. nucleatum on metaboli...

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Main Authors: Feiran Li, Huiying Huang, Jing Xu, Lei Tao, Liang Zhou, Chiyao Hsueh, Hongli Gong, Ming Zhang
Format: Article
Language:English
Published: Springer 2023-07-01
Series:Discover Oncology
Subjects:
Online Access:https://doi.org/10.1007/s12672-023-00727-x
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author Feiran Li
Huiying Huang
Jing Xu
Lei Tao
Liang Zhou
Chiyao Hsueh
Hongli Gong
Ming Zhang
author_facet Feiran Li
Huiying Huang
Jing Xu
Lei Tao
Liang Zhou
Chiyao Hsueh
Hongli Gong
Ming Zhang
author_sort Feiran Li
collection DOAJ
description Abstract Background Fusobacterium nucleatum (F. nucleatum) is a vital pro-oncogenic bacterium. Our previous study revealed that a high abundance of F. nucleatum in head and neck squamous cell carcinoma (HNSCC) is correlated with poor patient prognosis. However, the impact of F. nucleatum on metabolic reprogramming and tumor progression in HNSCC awaits more exploration. Methods Liquid chromatography‒mass spectrometry (LC‒MS) was applied to analyze the altered metabolites in a head and neck carcinoma cell line (AMC-HN-8) after coculture with F. nucleatum for 24 hrs and 48 hrs. Both univariate and multivariate analyses were used to screen for differential metabolites. Kyoto Encyclopedia of Genes and Genomes (KEGG) metabolic pathway enrichment analysis was further used to explore the metabolic changes. Results We observed a significantly altered metabolic profile in AMC-HN-8 cells over time after coculture with F. nucleatum. Among the several enriched pathways, the purine metabolic pathway was the most significantly enriched (P = 0.0005), with downregulation of purine degradation. Furthermore, uric acid, the end product of purine metabolism, significantly reversed F. nucleatum-triggered tumor progression and altered the intracellular reactive oxygen species (ROS) level. Moreover, the negative correlation between the serum uric acid level and the abundance of F. nucleatum was verified in 113 HNSCC patients (P = 0.0412, R = − 0.1924). Conclusions Our study revealed obviously aberrant purine metabolism driven by F. nucleatum in HNSCC, which was closely related to tumor progression and patient prognosis. These findings indicate the possibility of targeting F. nucleatum-induced purine metabolism reprogramming in the future treatment of HNSCC.
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spelling doaj.art-ec330808871e4759868c6921f98a06052023-07-02T11:19:25ZengSpringerDiscover Oncology2730-60112023-07-0114111210.1007/s12672-023-00727-xFusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinomaFeiran Li0Huiying Huang1Jing Xu2Lei Tao3Liang Zhou4Chiyao Hsueh5Hongli Gong6Ming Zhang7Department of Otorhinolaryngology, Eye & ENT Hospital, Fudan UniversityDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan UniversityDepartment of Nursing, Eye & ENT Hospital, Fudan UniversityDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan UniversityDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan UniversityDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan UniversityDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan UniversityDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan UniversityAbstract Background Fusobacterium nucleatum (F. nucleatum) is a vital pro-oncogenic bacterium. Our previous study revealed that a high abundance of F. nucleatum in head and neck squamous cell carcinoma (HNSCC) is correlated with poor patient prognosis. However, the impact of F. nucleatum on metabolic reprogramming and tumor progression in HNSCC awaits more exploration. Methods Liquid chromatography‒mass spectrometry (LC‒MS) was applied to analyze the altered metabolites in a head and neck carcinoma cell line (AMC-HN-8) after coculture with F. nucleatum for 24 hrs and 48 hrs. Both univariate and multivariate analyses were used to screen for differential metabolites. Kyoto Encyclopedia of Genes and Genomes (KEGG) metabolic pathway enrichment analysis was further used to explore the metabolic changes. Results We observed a significantly altered metabolic profile in AMC-HN-8 cells over time after coculture with F. nucleatum. Among the several enriched pathways, the purine metabolic pathway was the most significantly enriched (P = 0.0005), with downregulation of purine degradation. Furthermore, uric acid, the end product of purine metabolism, significantly reversed F. nucleatum-triggered tumor progression and altered the intracellular reactive oxygen species (ROS) level. Moreover, the negative correlation between the serum uric acid level and the abundance of F. nucleatum was verified in 113 HNSCC patients (P = 0.0412, R = − 0.1924). Conclusions Our study revealed obviously aberrant purine metabolism driven by F. nucleatum in HNSCC, which was closely related to tumor progression and patient prognosis. These findings indicate the possibility of targeting F. nucleatum-induced purine metabolism reprogramming in the future treatment of HNSCC.https://doi.org/10.1007/s12672-023-00727-xHead and neck carcinomaFusobacterium nucleatumMetabolic reprogrammingPurine metabolic pathwayPrognosis
spellingShingle Feiran Li
Huiying Huang
Jing Xu
Lei Tao
Liang Zhou
Chiyao Hsueh
Hongli Gong
Ming Zhang
Fusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma
Discover Oncology
Head and neck carcinoma
Fusobacterium nucleatum
Metabolic reprogramming
Purine metabolic pathway
Prognosis
title Fusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma
title_full Fusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma
title_fullStr Fusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma
title_full_unstemmed Fusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma
title_short Fusobacterium nucleatum-triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma
title_sort fusobacterium nucleatum triggered purine metabolic reprogramming drives tumorigenesis in head and neck carcinoma
topic Head and neck carcinoma
Fusobacterium nucleatum
Metabolic reprogramming
Purine metabolic pathway
Prognosis
url https://doi.org/10.1007/s12672-023-00727-x
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