Evidence map›Paper›PMID 40468018›Full record

ArticleVirchows Archiv : an international journal of pathology2025

EPM2 AIP1 immunohistochemistry as a surrogate of promoter methylation analysis in endometrial carcinoma.

Sonia Gatius, Marta Vaquero, Oliver Scheiber, Ana Velasco, Dolors Cuevas, Karl Kashofer, Maria Santacana, Núria Eritja, Sigurd Lax, Xavier Matias-Guiu

Abstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

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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

10 authors.

Sonia GatiusHospital Universitari Arnau de Vilanova. IRBLleida, Universitat de Lleida, Av Rovira Roure 80, CIBERONC, Lleida, 25198, Spain. sonia.gatius@udl.cat.ORCID http://orcid.org/0000-0002-1636-6010
Marta VaqueroHospital Universitari Arnau de Vilanova. IRBLleida, Universitat de Lleida, Av Rovira Roure 80, CIBERONC, Lleida, 25198, Spain.
Oliver ScheiberDepartment of Pathology, General Hospital Graz II, Styrian Hospital Corporation, Graz, Austria.
Ana VelascoHospital Universitari Arnau de Vilanova. IRBLleida, Universitat de Lleida, Av Rovira Roure 80, CIBERONC, Lleida, 25198, Spain.
Dolors CuevasHospital Universitari Arnau de Vilanova. IRBLleida, Universitat de Lleida, Av Rovira Roure 80, CIBERONC, Lleida, 25198, Spain.
Karl KashoferDiagnostic & Research Institute of Pathology, Medical University of Graz, Graz, Austria.
Maria SantacanaScientific and Technical Service of Immunohistochemistry, Lleida Institute for Biomedical Research Dr. Pifarré Foundation, IRBLleida, Hospital Universitari Arnau de Vilanova, Av. Alcalde Rovira Roure, 80, Lleida, 25198, Spain.
Núria EritjaOncologic Pathology Group, Department of Medicine and Surgery, Biomedical Research Institute of Lleida (IRBLleida), University of Lleida, Av. Rovira Roure 80, Lleida, 25198, Spain.
Sigurd LaxDepartment of Pathology, General Hospital Graz II, Styrian Hospital Corporation, Graz, Austria.
Xavier Matias-GuiuHospital Universitari Arnau de Vilanova. IRBLleida, Universitat de Lleida, Av Rovira Roure 80, CIBERONC, Lleida, 25198, Spain. xavier.matias@udl.cat.

Funding

CIBERONC CB16/12/00231Fundación Científica Asociación Española Contra el Cáncer GCTRA1804MATIgrup de cáncer Ginecològic i afins 2021 SGR 0093ISCIII PI23/00035Platform of Biobanks of ISCIII PT 23/0032
6 · The paper itself

Abstract

Mismatch repair (MMR) status in endometrial carcinoma (EC) is crucial for diagnosis, prognosis, treatment, and Lynch syndrome pre-screening. MLH1 loss is the most frequent cause of MMR deficiency and usually by promoter hypermethylation. We tried to confirm the role of EPM2 AIP1 immunohistochemistry as a surrogate of MLH1 promoter methylation in EC. Case series from two different institutions were analyzed by comparable methods using immunohistochemistry for MMR proteins and EPM2 AIP1, and pyrosequencing for MLH1 methylation. In the first series of 70 cases, concordance was 100%, after reassessing three cases with methylation scores close to cut-off, by tumor cell enrichment. In the second series of 29 MLH1-deficient ECs, concordance was 96.5%, while in the control group of 30 MMR-proficient EC, one MLH1-positive case was EPM2 AIP1-negative. EPM2 AIP1 immunoreactivity was qualitatively superior in curettages and biopsies compared to hysterectomy. We conclude that EPM2 AIP1 immunohistochemistry is a good surrogate for MLH1 promoter methylation analysis, cost-effective with short turnaround time, but needs attention regarding preanalytical handling, normal tissue contamination, or low tumor percentage.

Indexed as

Biomarkers, TumorCarrier ProteinsDNA MethylationEndometrial NeoplasmsImmunohistochemistryPromoter Regions, GeneticAdultAgedAged, 80 and overDNA Mismatch RepairFemaleHumansMiddle AgedMutL Protein Homolog 1Biomarkers, TumorCarrier ProteinsMLH1 protein, humanMutL Protein Homolog 1Endometrial cancerEPM2AIP1Lynch syndromeMLH-1 methylation

Identifiers

PMID40468018
PMCPMC12488810

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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.