Evidence map›Paper›PMID 41413813›Full record

ArticleBMC women's health2025

Exploring Nectin-4 as a potential diagnostic biomarker in endometrial adenocarcinoma : Title page.

Melike Ordu, Serife Ozlem Genc

Abstract read
In one paragraph

Article in BMC women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

2 authors.

Melike OrduDepartment of Pathology, Aksaray University Faculty of Medicine, Aksaray, Turkey.ORCID 0000-0001-8863-817X
Serife Ozlem GencDepartment of Obstetrics and Gynecology, Sivas Cumhuriyet University Faculty of Medicine, Sivas, Turkey. drserifeozlemgenc@gmail.com.ORCID 0000-0002-9811-2726

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study explored Nectin-4 expression in endometrial adenocarcinoma and examined its relationship with tumor grade, hormone receptor status, p53 expression, and mismatch repair (MMR) protein expression.

methodsWe retrospectively analyzed 55 paraffin-embedded tissue samples collected between 2015 and 2023, including endometrial adenocarcinoma, endometrial intraepithelial neoplasia (EIN), and normal endometrium samples. Nectin-4 expression was assessed via immunohistochemistry, and correlations with clinicopathological features and molecular markers were evaluated statistically.

resultsNectin-4 expression increased with histological grade (p < 0.001). All Grade III tumors presented strong expression, whereas lower-grade tumors presented variable staining. The expression of these genes was also correlated with p53 overexpression (p = 0.007) and PMS2 loss (p = 0.002). Nectin-4 was absent in normal tissues and weakly expressed in EIN.

conclusionNectin-4 expression is linked to high-grade endometrial carcinoma and abnormal p53 expression, supporting its potential role as a diagnostic biomarker. Larger studies are needed to validate its clinical use.

Indexed as

AdenocarcinomaBiomarkers, TumorCell Adhesion MoleculesEndometrial NeoplasmsNectinsAgedFemaleHumansImmunohistochemistryMiddle AgedNeoplasm GradingRetrospective StudiesTumor Suppressor Protein p53Biomarkers, TumorCell Adhesion MoleculesNECTIN4 protein, humanNectinsTumor Suppressor Protein p53Endometrial adenocarcinomaImmunohistochemistryMismatch repair proteinsNectin-4P53

Identifiers

PMID41413813
PMCPMC12825217

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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.