Evidence map›Paper›PMID 41239415›Full record

ArticleMolecular oncology2026

Methylation biomarkers can distinguish pleural mesothelioma from healthy pleura and other pleural pathologies.

Janah Vandenhoeck, Nele De Meulenaere, Thomas Vanpoucke, Joe Ibrahim, Dieter Peeters, Suresh Krishan Yogeswaran, Wen Wen, Paul Van Schil, Jeroen M H Hendriks, Jo Raskin and 3 more

Abstract read
In one paragraph

Article in Molecular oncology, 2026. 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

13 authors.

Janah VandenhoeckCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.ORCID https://orcid.org/0000-0003-2358-8671
Nele De MeulenaereCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.ORCID https://orcid.org/0000-0003-3390-5220
Thomas VanpouckeCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.
Joe IbrahimCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.ORCID https://orcid.org/0000-0001-9728-5273
Dieter PeetersDepartment of Pathology, Antwerp University Hospital and University of Antwerp, Edegem, Belgium.
Suresh Krishan YogeswaranDepartment of Thoracic and Vascular Surgery, Antwerp University Hospital, Edegem, Belgium.
Wen WenDepartment of Thoracic and Vascular Surgery, Antwerp University Hospital, Edegem, Belgium.
Paul Van SchilDepartment of Thoracic and Vascular Surgery, Antwerp University Hospital, Edegem, Belgium.
Jeroen M H HendriksDepartment of Thoracic and Vascular Surgery, Antwerp University Hospital, Edegem, Belgium.
Jo RaskinDepartment of Thoracic Oncology, Antwerp University Hospital and University of Antwerp, Edegem, Belgium.
Jan van MeerbeeckDepartment of Thoracic Oncology, Antwerp University Hospital and University of Antwerp, Edegem, Belgium.
Guy Van CampCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.ORCID https://orcid.org/0000-0001-5105-9000
Ken Op de BeeckCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.ORCID https://orcid.org/0000-0001-5527-6838

Funding

Fonds Wetenschappelijk Onderzoek 1S30125NStichting Tegen Kanker 46773Universiteit Antwerpen 39705Universiteit Antwerpen 40206Universiteit Antwerpen 50201
6 · The paper itself

Abstract

Pleural mesothelioma (PM) is a rare and aggressive cancer that often requires multiple diagnostic procedures before a definitive diagnosis can be made. To improve diagnostic accuracy, we developed a DNA methylation-based biomarker assay capable of distinguishing PM from healthy pleura and other pleural pathologies. Using Infinium EPIC array data, we identified 744 hypermethylated CpG sites in PM as candidate biomarkers. These were validated in silico using external datasets, yielding a high mean AUC of 0.935. Clinical validation was performed using IMPRESS, a novel bisulfite-free methylation detection technique that enables simultaneous analysis of thousands of CpG sites. A two-step classifier approach was applied: the first model differentiated tumoral from nontumoral pleura with 89.2% sensitivity and 93.5% specificity, while the second model distinguished PM from pleural metastases with 85.2% sensitivity and 100% specificity. These results demonstrate that our methylation-based biomarker panel offers a highly accurate and minimally invasive tool for differentiating PM from other pleural conditions, potentially streamlining the diagnostic process and improving clinical decision-making.

Indexed as

Biomarkers, TumorDNA MethylationMesotheliomaPleuraPleural NeoplasmsAgedCpG IslandsDiagnosis, DifferentialFemaleHumansMaleMesothelioma, MalignantMiddle AgedBiomarkers, Tumorcancer biomarkersDNA methylationpleural mesothelioma

Identifiers

PMID41239415
PMCPMC13060650

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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.