Evidence map›Paper›PMID 41828470›Full record

ArticleInternational journal of molecular sciences2026

Impact of Heterogeneous DNA Methylation on the Accuracy of Quantitative Methylation-Specific PCR for Detecting DNA Hypermethylation in Prostate Cancer.

Wieke C H Visser, Hans de Jong, Laureen B Janssen, Jolly Shrivastava, Peter F A Mulders, Jack A Schalken, Willem J G Melchers

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

7 authors.

Wieke C H VisserDepartment of Product Development, Mdxhealth BV, 6534 AT Nijmegen, The Netherlands.
Hans de JongDepartment of Product Development, Mdxhealth BV, 6534 AT Nijmegen, The Netherlands.
Laureen B JanssenDepartment of Product Development, Mdxhealth BV, 6534 AT Nijmegen, The Netherlands.
Jolly ShrivastavaDepartment of Product Development, Mdxhealth, Irvine, CA 92618, USA.
Peter F A MuldersDepartment of Medical Microbiology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Jack A SchalkenDepartment of Medical Microbiology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Willem J G MelchersDepartment of Urology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.ORCID 0000-0002-5446-2230

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation is an epigenetic modification of the genome, with methylation-based biomarkers showing promise for cancer detection. Quantitative Methylation-Specific PCR (qMSP) is widely used to assess DNA methylation; however, its application to liquid biopsy samples presents technical challenges. Heterogeneity in methylation patterns may impact qMSP accuracy by reducing reliability. This study evaluated the impact of methylation heterogeneity on qMSP performance using synthetic DNA fragments mimicking methylation variation. Additionally, targeted methylation sequencing was performed on prostate cancer tissue and urine samples to examine methylation heterogeneity. The presence of unmethylated CpG sites within the primer and probe regions reduced fluorescence levels and increased Cp values, especially at the 3'-end of primers. The methylation sequencing of genomic DNA from prostate cancer tissue and urine samples revealed the presence of varying methylation patterns, correlating with qMSP outcomes. Tissue samples mainly exhibited fully methylated and fully unmethylated fragments, while urine samples consisted of a higher proportion of partly methylated fragments. The findings suggest that qMSP may not be a reliable method for methylation detection in samples with proportionally high levels of heterogeneous methylated fragments in contrast to fully methylated fragments. This highlights the need for improved DNA methylation analysis in liquid biopsy samples for clinical applications in cancer detection.

Indexed as

DNA MethylationPolymerase Chain ReactionProstatic NeoplasmsBiomarkers, TumorCpG IslandsEpigenesis, GeneticHumansLiquid BiopsyMaleReproducibility of ResultsBiomarkers, TumorDNA methylationliquid biopsyprostate cancerqMSP

Identifiers

PMID41828470
PMCPMC12984612

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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 Socratic graph.