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ArticleMolecular biology reports2026

Exploratory transcriptomic analysis of low-grade oral epithelial dysplasia and oral squamous cell carcinoma in Chilean patients.

Mateus José Dutra, Patricio Miranda Cortes, Valentina Fernanda Fernández Díaz, Mauricio Alejandro Sáez Venegas, Sebastián Morales-Pison, Wilfredo Alejandro González-Arriagada, Ricardo Fernández-Ramires, Daniela Adorno-Farias

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Article in Molecular biology reports, 2026. 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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5 · Who and what money

Authors and funding

8 authors.

Mateus José DutraDepartment of Oral Diagnosis, Piracicaba Dental School, Universidade Estadual de Campinas, Piracicaba, São Paulo, Brazil.
Patricio Miranda CortesDepartment of Pathology and Oral Medicine, School of Dentistry, Universidad de Chile, Santiago, Chile.
Valentina Fernanda Fernández DíazDepartment of Pathology and Oral Medicine, School of Dentistry, Universidad de Chile, Santiago, Chile.
Mauricio Alejandro Sáez VenegasFacultad de Ciencias de la Salud, Universidad Católica de Temuco, Temuco, Chile.
Sebastián Morales-PisonPrecision Oncology Center, School of Medicine and Health Sciences, Universidad Mayor, Santiago, Chile.
Wilfredo Alejandro González-ArriagadaSchool of Dentistry, Universidad de los Andes, Santiago, Chile.
Ricardo Fernández-RamiresSchool of Medicine and Health Sciences, Universidad Mayor, Santiago, Chile.
Daniela Adorno-FariasDepartment of Pathology and Oral Medicine, School of Dentistry, Universidad de Chile, Santiago, Chile. dardorno@odontologia.uchile.cl.

Funding

Funds for Research in Dentistry (FIOUCH), Chile. S19-14
6 · The paper itself

Abstract

backgroundTo explore and characterize gene expression patterns and RNA-seq-derived sequence variation in samples from Chilean patients with low-grade oral epithelial dysplasia (LG-OED) and oral squamous cell carcinoma (OSCC). METHODS AND

resultsTranscriptome sequencing was performed on pooled samples of 5 LG-OED and compared with 5 OSCC and healthy oral mucosa tissue. Subsequently, a variation analysis of the transcriptome was conducted, along with functional classification of the most enriched signaling pathways. Dysregulated genes were found in both LG-OED and OSCC compared to the control groups. The most overexpressed genes were KRTAP5-4, LCE3B, DDX3Y, KDM5D, and MYH2, while the most repressed genes were TYRP1, HS3ST6, SNORA20, KRT76, TGM7, and SOX21 in LG-OED and OSCC, respectively. A large proportion of the identified variants were single nucleotide polymorphisms (SNPs). Based on frameshift effects, missense mutations were the most common. The most enriched signaling pathways in LG-OED were the Hippo, NOTCH, and TGF-beta pathways; in OSCC, the NRF2, TGF-beta, and PI3K pathways.

conclusionsThis exploratory study provides an initial molecular characterization of LG-OED and OSCC in Chilean patients, identifying candidate transcriptomic alterations and RNA-seq-derived variants that may contribute to understanding early oral carcinogenesis in this underrepresented population.

Indexed as

Carcinoma, Squamous CellMouth NeoplasmsAgedChileFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiddle AgedMouth MucosaPolymorphism, Single NucleotideSignal TransductionTranscriptomeGenetic ProfileOral LeukoplakiaPrognosisSquamous Cell Carcinoma of the Head and Neck

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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.