Evidence map›Paper›PMID 40439366›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

Mismatch Repair Proteins Immunostaining in Lip Squamous Cell Carcinoma: A Role in Lip Carcinogenesis?

Yamyle Velasquez Barragán, Anna Clara Aragao Matos Carlos, Gabriella Alves Juliao Costa, Osias Vieira Oliveira Filho, Thâmara Manoela Marinho Bezerra, Sergio Ferreira Juaçaba, Thinali Sousa Dantas, Ana Paula Negreiros Nunes Alves, Paulo Goberlânio De Barros Silva

Abstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 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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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Yamyle Velasquez BarragánDivision of Oral Pathology, Faculty of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Ceará, Brazil.
Anna Clara Aragao Matos CarlosDivision of Oral Pathology, Faculty of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Ceará, Brazil.
Gabriella Alves Juliao CostaDepartment of Dentistry, Unichristus, Rua João Adolfo Gurgel 133, Fortaleza, Ceará, Brazil.ORCID 0000-0001-6183-8884
Osias Vieira Oliveira FilhoDivision of Oral Pathology, Faculty of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Ceará, Brazil.ORCID 0000-0002-9046-3783
Thâmara Manoela Marinho BezerraDivision of Oral Pathology, Faculty of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Fortaleza, Ceará, Brazil.ORCID 0000-0002-2435-7106
Sergio Ferreira JuaçabaDivision of Cancerology, University of Oxford, England, United Kingdom and Doctor, Hospital Haroldo Juaçaba, Fortaleza, Ceará, Brazil.
Thinali Sousa DantasDivision of Oral Pathology, Faculty of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Fortaleza, Ceará, Brazil.
Ana Paula Negreiros Nunes AlvesDivision of Oral Pathology, Faculty of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Fortaleza, Ceará, Brazil.
Paulo Goberlânio De Barros SilvaDivision of Oral Pathology, Faculty of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Fortaleza, Ceará, Brazil.ORCID 0000-0002-1513-9027

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveLip squamous cell carcinoma (LSCC) is associated with malignant transformation of actinic cheilitis (AC). Since solar radiation alters the functions of mismatch repair (MMR) complex, we evaluated for their possible role in lip carcinogenesis. MATERIALS AND

methodsSamples of normal lip epithelia (NLE) (n=15), AC (n=30), and LSCC (n=45) were subjected to immunohistochemistry for MutSα (MSH2/MSH6) and MutLα (MLH1/PMS2) to assess the percentage (brown nuclei over all the keratinocytes in NLE and AC or all tumoral cells in LSCC) of nuclear positive cells and MSH2/MSH6 (MutSα-imbalance) and MLH1/PMS2 (MutLα-imbalance) ratios. Clinical-prognostic variables of the primary tumor and histopathological gradation (LSCC and AC) were evaluated. Mann-Whitney, Kruskal-Wallis/Dunn, and Spearman correlation tests were used (p<0.05, SPSS 20.0).

resultsLSCC and AC showed significant increases in MSH2 (p<0.001), MSH6 (p<0.001), MLH1 (p=0.040) percentage of immunostained cells, and MutSα-imbalance (p<0.001). MutSα-imbalance in AC was higher than MutLα-imbalance (p=0.028). In LSCC, T3/T4 tumors showed higher MutSα-imbalance (p=0.028) and MutLα-imbalance (p=0.014). In LSCC with nodal metastasis, the MutLα-imbalance was significantly higher than the MutSα-imbalance (p=0.046). AC with high-risk dysplasia (p=0.024) and LSCC with vascular invasion (p=0.035) showed lower immunostaining for MSH6. Direct correlations between MMR-proteins increased in LSCC.

conclusionsIncreased MMR expression in lip cancer and the imbalance between MutSa and MutLα is associated with the progression and prognosis of LSCC.

Indexed as

Biomarkers, TumorCarcinogenesisCarcinoma, Squamous CellCheilitisDNA-Binding ProteinsDNA Mismatch RepairLip NeoplasmsMutS Homolog 2 ProteinAdultAgedFemaleFollow-Up StudiesHumansImmunohistochemistryMaleMiddle AgedBiomarkers, TumorDNA-Binding ProteinsG-T mismatch-binding proteinMismatch Repair Endonuclease PMS2MLH1 protein, humanMSH2 protein, humanMutL Protein Homolog 1MutS Homolog 2 ProteinPMS2 protein, humanLip NeoplasmsMutL ProteinsMutS Proteins

Identifiers

PMID40439366
PMCPMC12290205

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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.