Evidence map›Paper›PMID 34454584›Full record

ArticleClinical epigenetics2021

Longitudinal analysis of individual cfDNA methylome patterns in metastatic prostate cancer.

Romina Silva, Bruce Moran, Anne-Marie Baird, Colm J O'Rourke, Stephen P Finn, Ray McDermott, William Watson, William M Gallagher, Donal J Brennan, Antoinette S Perry

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  5. Targeting tumor transition windows.Exploration of targeted anti-tumor therapy · 2026
    Review
  6. Article
  7. Review
  8. Article
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  11. Article
  12. Review
  13. Article
  14. Article
  15. Liquid biopsy to personalize treatment for metastatic prostate cancer.American journal of translational research · 2024
    Review
  16. Article
  17. Article
  18. NAR cancer · 2023
    Article
  19. Article
  20. Review
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

10 authors at 5 institutions in 2 countries.

Romina SilvaCancer Biology and Therapeutics Laboratory, UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
Bruce MoranDepartment of Pathology, St. Vincent's University Hospital, Dublin, Ireland.
Anne-Marie BairdDepartment of Clinical Medicine, Trinity College, Dublin, Ireland.
Colm J O'RourkeBiotech Research and Innovation Centre, Department of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Stephen P FinnDepartment of Clinical Medicine, Trinity College, Dublin, Ireland.
Ray McDermottCancer Trials Ireland, Dublin, Ireland.
William WatsonSchool of Medicine, University College Dublin, Dublin, Ireland.
William M GallagherCancer Biology and Therapeutics Laboratory, UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
Donal J BrennanCancer Biology and Therapeutics Laboratory, UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
Antoinette S PerryCancer Biology and Therapeutics Laboratory, UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland. antoinette.perry@ucd.ie.ORCID 0000-0002-6108-512X
University College Dublin · IETrinity College Dublin · IECancer Trials Ireland · IESt. Vincent's University Hospital · IEUniversity of Copenhagen · DK

Funding

irish cancer society CRS17SILirish cancer society (ie) PCT13MCDScience Foundation Ireland 15/IA/3104Science Foundation Ireland 18/SPP/3522
6 · The paper itself

Abstract

backgroundDisease progression and therapeutic resistance are hallmarks of advanced stage prostate cancer (PCa), which remains a major cause of cancer-related mortality around the world. Longitudinal studies, coupled with the use of liquid biopsies, offer a potentially new and minimally invasive platform to study the dynamics of tumour progression. Our aim was to investigate the dynamics of personal DNA methylomic profiles of metastatic PCa (mPCa) patients, during disease progression and therapy administration.

resultsForty-eight plasma samples from 9 mPCa patients were collected, longitudinally, over 13-21 months. After circulating cell-free DNA (cfDNA) isolation, DNA methylation was profiled using the Infinium MethylationEPIC BeadChip. The top 5% most variable probes across time, within each individual, were utilised to study dynamic methylation patterns during disease progression and therapeutic response. Statistical testing was carried out to identify differentially methylated genes (DMGs) in cfDNA, which were subsequently validated in two independent mPCa (cfDNA and FFPE tissue) cohorts. Individual cfDNA global methylation patterns were temporally stable throughout the disease course. However, a proportion of CpG sites presented a dynamic temporal pattern that was consistent with clinical events, including different therapies, and were prominently associated with genes linked to immune response pathways. Additionally, study of the tumour fraction of cfDNA identified > 2000 DMGs with dynamic methylation patterns.

conclusionsLongitudinal assessment of cfDNA methylation in mPCa patients unveiled dynamic patterns associated with disease progression and therapy administration, thus highlighting the potential of using liquid biopsies to study PCa evolution at a methylomic level.

Indexed as

EpigenomeAgedBiomarkers, TumorDNA MethylationEpigenesis, GeneticGene Expression Regulation, NeoplasticHumansIrelandLongitudinal StudiesMaleMiddle AgedNeoplasm MetastasisProstatic NeoplasmsBiomarkers, TumorcfDNADNA methylationLiquid biopsyLongitudinal studyMetastatic prostate cancer

Identifiers

PMID34454584
PMCPMC8403420
OpenAlexW3197330133

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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.