Systematic analyses uncover robust salivary microbial signatures and host-microbiome perturbations in oral squamous cell carcinoma.

IF 4.6 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2025-02-18 Epub Date: 2025-01-28 DOI:10.1128/msystems.01247-24
Zewen Han, Yichen Hu, Xin Lin, Hongyu Cheng, Biao Dong, Xuan Liu, Buling Wu, Zhenjiang Zech Xu
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Abstract

Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as Streptococcus, Lactobacillus, Prevotella, Bulleidia moorei, and Haemophilus in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection.

Importance: The oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.

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系统的分析揭示了口腔鳞状细胞癌中唾液微生物特征和宿主微生物组的扰动。
口腔鳞状细胞癌(OSCC)是口腔颌面部常见的恶性肿瘤,预后较差。口腔微生物群在这种疾病的发病机制中起着潜在的作用。然而,个别研究的结果并不一致,对oscc相关微生物群失调的全面了解仍然难以捉摸。在这里,我们通过整合11个公开可用的数据集进行了大规模的荟萃分析,这些数据集包括OSCC患者和健康对照者的唾液微生物组概况。在校正批次效应后,我们观察到与健康对照组相比,OSCC唾液微生物组中的α多样性和β多样性模式显著提高。利用随机效应模型,我们确定了跨数据集与OSCC相关的强大微生物特征,包括在OSCC样本中丰富的类群,如链球菌、乳酸杆菌、普雷沃氏菌、摩尔氏布氏菌和嗜血杆菌。从这些微生物标记物构建的机器学习模型准确地预测了OSCC状态,突出了它们作为非侵入性诊断生物标记物的潜力。有趣的是,我们的分析显示,正常唾液微生物组中与年龄和性别相关的特征在OSCC中被破坏,这表明复杂的宿主-微生物相互作用受到了干扰。总的来说,我们的发现揭示了OSCC口腔微生物组的复杂变化,为疾病病因学提供了新的见解,并为基于微生物组的诊断和治疗策略铺平了道路。鉴于唾液微生物组可以反映宿主的整体健康状况,并且唾液采样是一种安全、无创的方法,因此在高危OSCC人群中进行更广泛的唾液微生物组筛选可能是值得的,这对早期发现具有重要意义。重要性:口腔内有多种多样的微生物群落,对全身和口腔健康起着至关重要的作用。积累的研究表明,唾液微生物群与口腔癌相关的显著差异表明,微生物群失调可能与口腔鳞状细胞癌(OSCC)的发病机制有关。然而,与OSCC相关的特定微生物改变仍然存在争议。这项荟萃分析揭示了唾液微生物组的强大改变。使用差分操作分类单元的机器学习模型准确地预测了OSCC状态,突出了唾液微生物组作为非侵入性诊断生物标志物的潜力。有趣的是,正常唾液微生物组中与年龄和性别相关的特征在OSCC中被破坏,表明宿主-微生物相互作用受到干扰。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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