Oral microbiome-derived biomarkers for non-invasive diagnosis of head and neck squamous cell carcinoma.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jingtai Zhi, Yibo Liang, Wang Zhao, Jie Qiao, Yongzhe Zheng, Xin Peng, Li Li, Xianfeng Wei, Wei Wang
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引用次数: 0

Abstract

Mounting evidence suggests that sustained microbial dysbiosis is associated with the development of multiple cancers, while the species-level bacterial taxa and metabolic dysfunction of oral microbiome in patients with head and neck squamous cell carcinoma (HNSCC) remains unclear. In this cross-sectional study, comprehensive metagenomic and 16S rRNA amplicon sequencing analyses of oral swab samples from 172 patients were performed. Unsupervised clustering algorithms of relative microbial abundance profiles revealed three distinctive microbiome clusters. Based on the metagenomic and 16S rRNA amplicon sequencing data, machine learning-based methods were used to construct the HNSCC diagnostic classifier, which exhibited high area under the curve values of 0.78-0.89. Our study provided the first exhaustive metagenomic and 16S rRNA amplicon sequencing analyses to date, revealing that microbial-metabolic dysbiosis is a potential risk factor for HNSCC progression and therefore providing a robust theoretical basis for potential diagnostic and therapeutic strategies for HNSCC patients.

口腔微生物来源的生物标志物用于头颈部鳞状细胞癌的非侵入性诊断。
越来越多的证据表明,持续的微生物生态失调与多种癌症的发展有关,而头颈部鳞状细胞癌(HNSCC)患者口腔微生物组的物种水平细菌分类群和代谢功能障碍尚不清楚。在这项横断面研究中,对172例患者的口腔拭子样本进行了全面的宏基因组和16S rRNA扩增子测序分析。相对微生物丰度的无监督聚类算法揭示了三种不同的微生物群。基于宏基因组和16S rRNA扩增子测序数据,采用基于机器学习的方法构建了HNSCC诊断分类器,该分类器曲线下面积为0.78 ~ 0.89。我们的研究提供了迄今为止第一个详尽的宏基因组和16S rRNA扩增子测序分析,揭示了微生物代谢失调是HNSCC进展的潜在危险因素,因此为HNSCC患者的潜在诊断和治疗策略提供了强有力的理论基础。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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