Evidence map›Paper›PMID 41091430›Full record

ArticleDiscover oncology2025

Integrated bioinformatics analysis of common molecular mechanisms and biomarkers in oral squamous cell carcinoma and periodontal disease.

Lin Wu, Peng She, Chenguang Qiu, Hongtao Sun, Fanzhi Kong, Hong Wang, Yu Tian, Jun Yang, Zhenwei Mao

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Lin WuDepartment of Stomatology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Peng SheDepartment of Stomatology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Chenguang QiuDepartment of Stomatology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Hongtao SunDepartment of Stomatology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Fanzhi KongDepartment of Stomatology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Hong WangDepartment of Stomatology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Yu TianDepartment of Stomatology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Jun YangDepartment of Laboratory Medicine, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China. 343321586@qq.com.
Zhenwei MaoDepartment of Laboratory Medicine, Fourth Affiliated People's Hospital of Jiangsu University, Zhenjiang, China. maopen365@163.com.

Funding

Key research and development Program of Zhenjiang City SH2023036Key research and development Program of Zhenjiang City SH2024005Key research and development Program of Zhenjiang City SH2024012Open Project of Jiangsu Provincial Key Laboratory of Laboratory Medicine, Jiangsu University JSKLM-Y-2024-011
6 · The paper itself

Abstract

backgroundOral Squamous Cell Carcinoma (OSCC) and Periodontal Disease (PD) are two distinct yet interconnected conditions with complex molecular mechanisms. This study aimed to analyze transcriptomic data from both diseases to identify common and unique molecular features, uncover potential biomarkers, and explore therapeutic targets.

methodTranscriptomic data from OSCC and PD were analyzed using WGCNA to construct gene co-expression networks and identify disease-associated modules. Functional enrichment analyses were conducted to reveal shared biological pathways, particularly those related to extracellular matrix organization. Machine learning methods, including Lasso regression, Random Forest, and SVM-RFE, were applied to select key feature genes. The findings were validated using independent datasets. Immune infiltration analysis using CIBERSORT was performed to assess immune cell interactions, while single-cell RNA sequencing was employed to explore the cellular distribution and functional role of the identified biomarker FNDC3B.

resultWGCNA identified key gene modules associated with OSCC and PD, with functional enrichment analyses highlighting shared pathways involved in extracellular matrix organization. Machine learning approaches identified FNDC3B as a central gene in both diseases, and its differential expression was validated in independent datasets. Immune infiltration analysis demonstrated the involvement of FNDC3B in immune cell interactions. Single-cell RNA sequencing further revealed the enrichment of FNDC3B in specific cell types, providing deeper insights into its role in disease progression.

conclusionThis study elucidates the molecular similarities and differences between OSCC and PD, positioning FNDC3B as a critical biomarker for both conditions. The findings enhance our understanding of the shared and distinct mechanisms driving these diseases and provide a foundation for the development of targeted therapeutic strategies.

Indexed as

FNDC3BImmune infiltrationMachine learningOral squamous cell carcinomaPeriodontal disease

Identifiers

PMID41091430
PMCPMC12528526

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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 OpenQuestion graph.