Evidence map›Paper›PMID 32918120›Full record

ArticleClinical oral investigations2021

Immune expression profile identification in a group of proliferative verrucous leukoplakia patients: a pre-cancer niche for oral squamous cell carcinoma development.

Carlos Llorens, Beatriz Soriano, Lucia Trilla-Fuertes, Leticia Bagan, Ricardo Ramos-Ruiz, Angelo Gamez-Pozo, Cristina Peña, Jose V Bagan

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In one paragraph

Article in Clinical oral investigations, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 17% of its field
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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Observational
  5. Review
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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

8 authors at 4 institutions in 1 country.

Carlos LlorensBiotechvana, Parc Científic, Universitat de València, Paterna, Valencia, Spain.
Beatriz SorianoBiotechvana, Parc Científic, Universitat de València, Paterna, Valencia, Spain.
Lucia Trilla-FuertesBiomedica Molecular Medicine SL, Madrid, Spain.
Leticia BaganMedicina Oral Unit, University General Hospital Valencia University, Valencia, Spain.
Ricardo Ramos-RuizGenomics Unit Cantoblanco, Parque Científico de Madrid, Madrid, Spain.
Angelo Gamez-PozoBiomedica Molecular Medicine SL, Madrid, Spain.
Cristina PeñaMedical Oncology Department, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), CIBERONC, Madrid, Spain. cristinapenamaroto@gmail.com.ORCID http://orcid.org/0000-0003-4406-8640
Jose V BaganMedicina Oral Unit, University General Hospital Valencia University, Valencia, Spain. jose.v.bagan@uv.es.
Hospital General Universitario De Valencia · ESParc Científic de la Universitat de València · ESHospital Universitario La Paz · ESInstituto Ramón y Cajal de Investigación Sanitaria · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo explore the pathophysiology of proliferative verrucous leukoplakia, a rare oral disorder that exhibits high rates of recurrence and malignant transformation, through a RNAseq case-control study. MATERIAL AND

methodsWe obtained oral biopsies from 10 patients with verrucous leukoplakia lesions and from the mucosa of 5 healthy individuals for sequencing using RNAseq technology. Using bioinformatic methods, we investigated gene expression and enrichment differences between patients both with and without the disorder. We applied network biology methods to investigate functional relations among those genes that were differentially deregulated.

resultsWe detected 140 differentially expressed genes with distinct roles in immune surveillance, tissue and organ morphogenesis, development, and organization. Of these 140 genes, 111 have been previously described as cancer expression biomarkers, being oral squamous cell carcinoma the most represented type of cancer among them. Of these 140 genes, 26 were prioritized for further investigation as biomarkers using larger sample sizes.

conclusionsThe gene expression patterns of healthy and unhealthy patients differed in 140 genes whose deregulation has a functional impact on normal functioning of the immune system. This immune expression profile provides a plausible hypothesis to explain the transformation to oral squamous cell carcinoma observed in 6 of the 10 assayed cases. CLINICAL RELEVANCE: By determining the molecular bases of the proliferative verrucous leukoplakia disorder and identifying early biomarkers of malignancy, this can allow us to develop new treatment strategies.

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsMouth NeoplasmsCase-Control StudiesCell Transformation, NeoplasticHumansLeukoplakia, OralNeoplasm Recurrence, LocalSquamous Cell Carcinoma of Head and NeckDifferential expressionFiber organizationGene ontologyImmune responseOral squamous cell carcinomaProliferative verrucous leukoplakiaProtein-protein interaction networks

Identifiers

PMID32918120
OpenAlexW3085480539

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Registered trials

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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.