Evidence map›Paper›PMID 39425144›Full record

ArticleClinical epigenetics2024

COL25A1 and METAP1D DNA methylation are promising liquid biopsy epigenetic biomarkers of colorectal cancer using digital PCR.

Alexis Overs, Paul Peixoto, Eric Hervouet, Chloé Molimard, Franck Monnien, Jules Durand, Michael Guittaut, Angélique Vienot, Julien Viot, Michael Herfs and 3 more

Abstract read
In one paragraph

Article in Clinical epigenetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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  7. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
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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

13 authors.

Alexis OversDepartment of Oncobiology, University Hospital of Besançon, 3 Boulevard Alexandre Fleming, 25000, Besançon, France. aovers@chu-besancon.fr.
Paul PeixotoUMR1098, INSERM, University of Bourgogne Franche-Comté, Besançon, France.
Eric HervouetUMR1098, INSERM, University of Bourgogne Franche-Comté, Besançon, France.
Chloé MolimardDepartment of Pathology, University Hospital of Besançon, 25000, Besancon, France.
Franck MonnienDepartment of Pathology, University Hospital of Besançon, 25000, Besancon, France.
Jules DurandUMR1098, INSERM, University of Bourgogne Franche-Comté, Besançon, France.
Michael GuittautUMR1098, INSERM, University of Bourgogne Franche-Comté, Besançon, France.
Angélique VienotDepartment of Oncology, University Hospital of Besançon, 25000, Besancon, France.
Julien ViotDepartment of Oncology, University Hospital of Besançon, 25000, Besancon, France.
Michael HerfsLaboratory of Experimental Pathology, GIGA-Cancer, University of Liege, Liège, Belgium.
Christophe BorgUMR1098, INSERM, University of Bourgogne Franche-Comté, Besançon, France.
Jean-Paul FeugeasDepartment of Oncobiology, University Hospital of Besançon, 3 Boulevard Alexandre Fleming, 25000, Besançon, France.
Zohair SelmaniDepartment of Oncobiology, University Hospital of Besançon, 3 Boulevard Alexandre Fleming, 25000, Besançon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer is a public health issue and was the third leading cause of cancer-related death worldwide in 2022. Early diagnosis can improve prognosis, making screening a central part of colorectal cancer management. Blood-based screening, diagnosis and follow-up of colorectal cancer patients are possible with the study of cell-free circulating tumor DNA. This study aimed to identify novel DNA methylation biomarkers of colorectal cancer that can be used for the follow-up of patients with colorectal cancer.

methodsA DNA methylation profile was established in the Gene Expression Omnibus (GEO) database (n = 507) using bioinformatics analysis and subsequently confirmed using The Cancer Genome Atlas (TCGA) database (n = 348). The in silico profile was then validated on local tissue and cell-free DNA samples using methylation-specific digital PCR in colorectal cancer patients (n = 35) and healthy donors (n = 35).

resultsThe DNA methylation of COL25A1 and METAP1D was predicted to be a colorectal cancer biomarker by bioinformatics analysis (ROC AUC = 1, 95% CI [0.999-1]). The two biomarkers were confirmed with tissue samples, and the combination of COL25A1 and METAP1D yielded 49% sensitivity and 100% specificity for cell-free DNA.

conclusionBioinformatics analysis of public databases revealed COL25A1 and METAP1D DNA methylation as clinically applicable liquid biopsies DNA methylation biomarkers. The specificity implies an excellent positive predictive value for follow-up, and the high sensitivity and relative noninvasiveness of a blood-based test make these biomarkers compatible with colorectal cancer screening. However, the clinical impact of these biomarkers in colorectal cancer screening and follow-up needs to be established in further prospective studies.

Indexed as

Biomarkers, TumorColorectal NeoplasmsDNA MethylationAgedCirculating Tumor DNAComputational BiologyEpigenesis, GeneticFemaleHumansLiquid BiopsyMaleMiddle AgedPolymerase Chain ReactionBiomarkers, TumorCirculating Tumor DNABiomarkerCirculating tumor DNACOL25A1Colorectal cancerDigital PCRDNA methylationLiquid biopsyMETAP1D

Identifiers

PMID39425144
PMCPMC11490026

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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.