Evidence map›Paper›PMID 41327157›Full record

ArticleBMC oral health2025

Saliva from oral squamous cell carcinoma patients promotes tumor progression via Inflammation, stromal remodeling, and metabolic reprogramming in a mouse model.

Xiao-Yan Zhang, Yuan-Tao Li, Jie Guo, Ying Feng, Qian Han, Shi-Han Zhang, Yu Gao, Hao-Tian Yin, Xiao-Xu Ding, Xiang-Jun Li and 1 more

Abstract read
In one paragraph

Article in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Xiao-Yan Zhang *School and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, China.
Yuan-Tao Li *School and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, China.
Jie GuoThe Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Ying FengSchool and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, China.
Qian HanHebei Medical University, Shijiazhuang, China.
Shi-Han ZhangSchool and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, China.
Yu GaoHebei Provincial Traditional Chinese Medicine Hospital, Shijiazhuang, China.
Hao-Tian YinSchool and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, China.
Xiao-Xu DingXinle Hospital of Traditional Chinese Medicine, Shijiazhuang, China.
Xiang-Jun LiSchool and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, China. lixiangjun@hebmu.edu.cn.
Bei-Bei LiangSchool and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, China. liangbeibei@hebmu.edu.cn.

Funding

Hebei Province Medical Science Research Project 20240101Hebei Provincial Government-Funded Clinical Medicine Talent Cultivation Program ZF2024151Hebei Provincial Government-Funded Clinical Medicine Talent Cultivation Program ZF2025241Research projects under the Hebei Provincial Administration of Traditional Chinese Medicine 2025350S&T Program of Hebei 25297704D
6 · The paper itself

Abstract

backgroundOral squamous cell carcinoma (OSCC) is a prevalent and aggressive malignancy with increasing evidence implicating the oral microbiome and tumor microenvironment in its progression. However, the mechanistic impact of OSCC patient-derived saliva on tumor development remains poorly understood.

methodsWe established an orthotopic OSCC mouse model and topically applied saliva collected from OSCC patients to assess its effects on tumor progression. Multi-omics analyses, including 16 S rRNA sequencing, tumor transcriptomics (RNA-seq), and metabolomics (LC-MS), were performed to explore changes in the oral microbiota, gene expression profiles, and metabolic pathways.

resultsTreatment with OSCC patient saliva significantly accelerated tumor growth compared to controls. Saliva application altered the oral microbiota, most notably causing a significant enrichment of the genus Staphylococcus. Tumor transcriptomics revealed upregulation of genes associated with chronic neutrophilic inflammation (Mpo), cancer-associated fibroblast (CAF) activation, and extracellular matrix (ECM) remodeling (Angptl4, Col2a1). Metabolomic analysis demonstrated profound metabolic reprogramming within the tumors, including enhanced amino acid metabolism (tryptophan, glutamate), fatty acid oxidation, and accumulation of the oncometabolite succinate. Integrated analysis showed that Staphylococcus abundance was strongly correlated with these inflammatory and metabolic signatures.

conclusionsThis study demonstrates that saliva from OSCC patients promotes tumor progression in vivo through a multifactorial mechanism involving inflammation, stromal remodeling, and metabolic rewiring. These findings highlight the tumor-promoting potential of salivary and microbial components, suggesting new avenues for diagnostic and therapeutic strategies targeting the oral microenvironment in OSCC.

Indexed as

Carcinoma, Squamous CellInflammationMouth NeoplasmsSalivaAnimalsDisease Models, AnimalDisease ProgressionHumansMaleMetabolic ReprogrammingMetabolomicsMiceMicrobiotaTumor Microenvironment16S rRNAMetabolomicsOral squamous cell carcinomaRNA-seqTumor microenvironment

Identifiers

PMID41327157
PMCPMC12771916

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.