Evidence map›Paper›PMID 39620930›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2025

Noninvasive Multicancer Detection Using DNA Hypomethylation of LINE-1 Retrotransposons.

Marc Michel, Maryam Heidary, Anissa Mechri, Kévin Da Silva, Marine Gorse, Victoria Dixon, Klaus von Grafenstein, Charline Bianchi, Caroline Hego, Aurore Rampanou and 14 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Trial
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  13. LINE-1 Retrotransposons as Cell-free DNA Biomarkers for Multicancer Early Detection.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
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

24 authors.

Marc Michel *Inserm U934, CNRS UMR3215, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0001-6613-8027
Maryam Heidary *Circulating Tumor Biomarkers Laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.ORCID 0009-0007-4240-7385
Anissa MechriInserm U934, CNRS UMR3215, Institut Curie, PSL Research University, Paris, France.ORCID 0009-0009-8985-9084
Kévin Da SilvaUniv Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) - UMR_S 1085, Rennes, France.ORCID 0000-0002-3022-5361
Marine GorseUniv Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) - UMR_S 1085, Rennes, France.ORCID 0009-0000-7693-1838
Victoria DixonUniv Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) - UMR_S 1085, Rennes, France.ORCID 0009-0005-5663-7902
Klaus von GrafensteinUniv Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) - UMR_S 1085, Rennes, France.ORCID 0000-0003-1667-060X
Charline BianchiUniv Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) - UMR_S 1085, Rennes, France.ORCID 0009-0000-9031-2873
Caroline HegoCirculating Tumor Biomarkers Laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.ORCID 0009-0002-4813-6137
Aurore RampanouCirculating Tumor Biomarkers Laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.ORCID 0009-0004-2154-6376
Constance LamyDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris, France.ORCID 0000-0003-0311-8031
Maud KamalDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris, France.ORCID 0000-0003-1466-0950
Christophe Le TourneauDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris, France.ORCID 0000-0001-9772-4686
Mathieu SénéPharmacogenomics Unit, Genetics Department, Institut Curie, Paris, France.ORCID 0009-0000-9342-8687
Ivan BièchePharmacogenomics Unit, Genetics Department, Institut Curie, Paris, France.ORCID 0000-0002-2430-5429
Cécile ReyesGenomics Platform, Translational Research Department, Research Center, Institut Curie, PSL Research University, Paris, France.ORCID 0009-0001-2281-0827
David GentienGenomics Platform, Translational Research Department, Research Center, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0001-8317-5188
Marc-Henri SternInserm U830, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0002-8100-2272
Olivier LantzInserm U932, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0003-3161-7719
Luc CabelDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.ORCID 0000-0001-5515-9180
Jean-Yves PiergaCirculating Tumor Biomarkers Laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.ORCID 0000-0002-2863-9995
François-Clément BidardCirculating Tumor Biomarkers Laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.ORCID 0000-0001-5932-8949
Chloé-Agathe AzencottCBIO-Center for Computational Biology, Mines Paris, PSL Research University, Paris, France.ORCID 0000-0003-1003-301X
Charlotte ProudhonInserm U934, CNRS UMR3215, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0002-4649-4574

Funding

Agence Nationale de la Recherche (ANR) ANR-19-P3IA-0001 (PRAIRIE 3IA Institute)HORIZON EUROPE European Research Council (ERC) ERC-StG EpiDetectInstitut des Sciences Biologiques (INSB) prematuration programLigue Contre le Cancer (French League Against Cancer) RS17-75-75
6 · The paper itself

Abstract

purposeThe detection of ctDNA, which allows noninvasive tumor molecular profiling and disease follow-up, promises optimal and individualized management of patients with cancer. However, detecting small fractions of tumor DNA released when the tumor burden is reduced remains a challenge. EXPERIMENTAL

designWe implemented a new, highly sensitive strategy to detect bp resolution methylation patterns from plasma DNA and assessed the potential of hypomethylation of long interspersed nuclear element-1 retrotransposons as a noninvasive multicancer detection biomarker. The Detection of Long Interspersed Nuclear Element Altered Methylation ON plasma DNA method targets 30 to 40,000 young long interspersed nuclear element-1 retrotransposons scattered throughout the genome, covering about 100,000 CpG sites and is based on a reference-free analysis pipeline.

resultsResulting machine learning-based classifiers showed powerful correct classification rates discriminating healthy and tumor plasmas from six types of cancers (colorectal, breast, lung, ovarian, and gastric cancers and uveal melanoma, including localized stages) in two independent cohorts (AUC = 88%-100%, N = 747). The Detection of Long Interspersed Nuclear Element Altered Methylation ON plasma DNA method can also be used to perform copy number alteration analysis that improves cancer detection.

conclusionsThis should lead to the development of more efficient noninvasive diagnostic tests adapted to all patients with cancer, based on the universality of these factors. See related commentary by Szymanski et al., p. 1179.

Indexed as

Biomarkers, TumorCirculating Tumor DNADNA MethylationLong Interspersed Nucleotide ElementsNeoplasmsCpG IslandsFemaleHumansMachine LearningMaleRetroelementsBiomarkers, TumorCirculating Tumor DNARetroelements

Identifiers

PMID39620930
PMCPMC11959274

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.