Evidence map›Paper›PMID 41635022›Full record

ArticleJournal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology2026

The Expression and Potential Role of MicroRNAs in Oral Lichen Planus.

Mousa Ali Heba, Resteu Anastasia, Werner Andreas, Carrozzo Marco

Abstract read
In one paragraph

Article in Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 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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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

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Mousa Ali HebaBiosciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Resteu AnastasiaTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Werner AndreasBiosciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Carrozzo MarcoOral Medicine Department, School of Dental Sciences, Newcastle University, Newcastle upon Tyne, UK.

Funding

Libyan Embassy
6 · The paper itself

Abstract

backgroundOral lichen planus (OLP) is a chronic T-cell-mediated immune disease of unknown aetiology. MicroRNA (miRNAs) are short non-coding RNAs capable of regulating mRNA and may have roles in T-cell-related diseases. The aim of this study was to investigate the profile of miRNAs in OLP patients and its interaction with potential target genes.

methodsTotal RNA was extracted from fresh frozen biopsies from 24 patients with OLP and 8 control patients. The NanoString Counter Analysis System was used to analyse total RNA samples for differential miRNA expression. NanoString expression was confirmed by RT-qPCR analysis. Genes potentially targeted by upregulated and downregulated miRNAs were identified, and RT-qPCR was employed to investigate the expression of target genes in OLP and controls. Probability values < 0.05 were considered statistically significant.

resultsNanoString analysis showed that eight miRNAs, miR-155, miR-146a, miR-3195, miR-342, miR-4516, miR-21, miR-29a and miR-193 were upregulated in OLP tissues. Contrarily, the other eight miRNAs, miR-221, miR-200b, miR-149, miR-205, miR-27b, miR-95, miR-127b, miR-95, miR-206 were downregulated in OLP tissues. NanoString findings have been confirmed by RT-qPCR results for four upregulated miRNAs, miR-155, miR-146a, miR-29a and miR-342, and one downregulated miRNA, namely miR-205. The expression of two target genes, namely MYC for miR-29a and interleukin-24 (IL-24) for miR-205, was found to negatively correlate with the respective miRNA. This suggests that MYC and IL-24 could be regulated by the above miRNAs in OLP.

conclusionsThe work presented in this study suggests that miRNAs could be involved in both the immunopathogenesis and malignant transformation of OLP.

Indexed as

Lichen Planus, OralMicroRNAsAdultAgedFemaleHumansMaleMiddle AgedUp-RegulationMicroRNAsmalignant transformationmicroRNAsoral lichen planuspathogenesis

Identifiers

PMID41635022
PMCPMC13333531

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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.