Evidence map›Paper›PMID 39858027›Full record

ArticleCancers2025

Genome-Wide DNA Methylation Confirms Oral Squamous Cell Carcinomas in Proliferative Verrucous Leukoplakia as a Distinct Oral Cancer Subtype: A Case-Control Study.

Alex Proaño, Gracia Sarrion-Perez, Leticia Bagan, Jose Bagan

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Alex ProañoMedicina Bucal Unit, Stomatology Department, Valencia University, 46010 Valencia, Spain.
Gracia Sarrion-PerezMedicina Bucal Unit, Stomatology Department, Valencia University, 46010 Valencia, Spain.
Leticia BaganMedicina Bucal Unit, Stomatology Department, Valencia University, 46010 Valencia, Spain.
Jose BaganMedicina Bucal Unit, Stomatology Department, Valencia University, 46010 Valencia, Spain.ORCID 0000-0002-0295-2916

Funding

Ministerio de Ciencia, Innovación y Universidades PID2022-138398OB-I00
6 · The paper itself

Abstract

BACKGROUND/

objectivesOral cancers in patients with proliferative verrucous leukoplakia (PVL-OSCC) exhibit different clinical and prognostic outcomes from those seen in conventional oral squamous cell carcinomas (cOSSCs). The aim of the present study is to compare the genome-wide DNA methylation signatures in fresh frozen tissues between oral squamous cell carcinomas in patients with PVL and cOSCC using the Illumina Infinium MethylationEPIC BeadChip.

methodsThis case-control study was carried out at the Stomatology and Maxillofacial Surgery Department of the General University Hospital of Valencia. For the epigenomic study, unsupervised exploratory bioinformatic analyses were performed using principal component and heatmap analysis. Supervised differential methylation analyses were conducted using a rank-based regression model and a penalized logistic regression model to identify potential prognostic biomarkers.

resultsThe unsupervised analyses of the global methylation profiles did not allow us to differentiate between the distinct oral cancer groups. However, the two supervised analyses confirmed the existence of two oral carcinoma phenotypes. We identified 21 differentially methylated CpGs corresponding to 14 genes. Among them, three CpGs had not been previously assigned to any known gene, and the remaining were associated with genes unrelated to oral cancer. The AGL, WRB, and ARL15 genes were identified as potential prognostic biomarkers.

conclusionsThis study emphasizes the significant role of epigenetic dysregulation in OSCC, particularly in cases preceded by PVL. We have provided data on differential methylation genes that could be involved in the molecular carcinogenesis of PVL-OSCC.

Indexed as

differential methylationDNA methylationoral squamous cell carcinomaprognosis biomarkersproliferative verrucous leukoplakia

Identifiers

PMID39858027
PMCPMC11763802

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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.