Evidence map›Paper›PMID 37309009›Full record

ArticleClinical epigenetics2023

Buffy coat signatures of breast cancer risk in a prospective cohort study.

Felicia Fei-Lei Chung, Sandra González Maldonado, Amelie Nemc, Liacine Bouaoun, Vincent Cahais, Cyrille Cuenin, Aurelie Salle, Theron Johnson, Bekir Ergüner, Marina Laplana and 12 more

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

22 authors at 9 institutions in 6 countries.

Felicia Fei-Lei Chung *International Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France. feliciacfl@sunway.edu.my.
Sandra González Maldonado *Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Amelie Nemc *CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Liacine Bouaoun *International Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France.
Vincent CahaisInternational Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France.
Cyrille CueninInternational Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France.
Aurelie SalleInternational Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France.
Theron JohnsonDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Bekir ErgünerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Marina LaplanaDivision of Cancer Epigenomics, German Cancer Research Center, Heidelberg, Germany.
Paul DatlingerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Jana JeschkeLaboratory of Cancer Epigenetics, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Elisabete WeiderpassInternational Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France.
Vessela KristensenFaculty of Medicine, Institute for Clinical Epidemiology and Molecular Biology, University of Oslo, Oslo, Norway.
Suzette DelalogeDepartment of Cancer Medicine, Institut Gustave Roussy, Villejuif, France.
François FuksLaboratory of Cancer Epigenetics, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Angela RischDivision of Cancer Epigenomics, German Cancer Research Center, Heidelberg, Germany.
Akram GhantousInternational Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France.
Christoph PlassDivision of Cancer Epigenomics, German Cancer Research Center, Heidelberg, Germany.
Christoph Bock *CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Rudolf Kaaks *Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Zdenko Herceg *International Agency for Research On Cancer (IARC), 25 avenue Tony Garnier, CS 90627, 69366, Lyon, France. hercegz@iarc.who.int.
Centre International de Recherche sur le Cancer · FRGerman Cancer Research Center · DEHeidelberg University · DEAustrian Academy of Sciences · ATUniversité Libre de Bruxelles · BEAustrian Research Institute for Artificial Intelligence · ATCeMM Research Center for Molecular Medicine · ATInstitut Gustave Roussy · FRUniversity of Oslo · NO

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundEpigenetic alterations are a near-universal feature of human malignancy and have been detected in malignant cells as well as in easily accessible specimens such as blood and urine. These findings offer promising applications in cancer detection, subtyping, and treatment monitoring. However, much of the current evidence is based on findings in retrospective studies and may reflect epigenetic patterns that have already been influenced by the onset of the disease.

methodsStudying breast cancer, we established genome-scale DNA methylation profiles of prospectively collected buffy coat samples (n = 702) from a case-control study nested within the EPIC-Heidelberg cohort using reduced representation bisulphite sequencing (RRBS).

resultsWe observed cancer-specific DNA methylation events in buffy coat samples. Increased DNA methylation in genomic regions associated with SURF6 and REXO1/CTB31O20.3 was linked to the length of time to diagnosis in the prospectively collected buffy coat DNA from individuals who subsequently developed breast cancer. Using machine learning methods, we piloted a DNA methylation-based classifier that predicted case-control status in a held-out validation set with 76.5% accuracy, in some cases up to 15 years before clinical diagnosis of the disease.

conclusionsTaken together, our findings suggest a model of gradual accumulation of cancer-associated DNA methylation patterns in peripheral blood, which may be detected long before clinical manifestation of cancer. Such changes may provide useful markers for risk stratification and, ultimately, personalized cancer prevention.

Indexed as

Breast NeoplasmsCase-Control StudiesDNA MethylationFemaleHumansNuclear ProteinsProspective StudiesRetrospective StudiesNuclear ProteinsSURF6 protein, humanBreast cancerCancer risk markersDNA methylationEpigeneticsProspective cohort

Identifiers

PMID37309009
PMCPMC10262593
OpenAlexW4380369675

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.