ArticleDiscover oncology2025
Integrated bioinformatics analysis of common molecular mechanisms and biomarkers in oral squamous cell carcinoma and periodontal disease.
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.
What it found
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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.
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.
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Who cites it
2 citing papers in PubMed.
- Immunological Analysis of Oral Cytobrush Specimens for Early Detection of Oral Cancer Biomarkers: A Comprehensive Review.International journal of molecular sciences · 2026Review
- Multifaceted roles of fibronectin type III domain containing 3B (FNDC3B) in cell biology and signaling.Frontiers in molecular biosciences · 2026Review
Corrections and comments
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Authors and funding
9 authors.
Funding
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.
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Registered trials
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