Evidence map›Paper›PMID 39095452›Full record

ArticleScientific reports2024

Detection of differentially methylated CpGs between tumour and adjacent benign cells in diagnostic prostate cancer samples.

Liesel M FitzGerald, Chol-Hee Jung, Ee Ming Wong, JiHoon E Joo, Julie K Bassett, James G Dowty, Xiaoyu Wang, James Y Dai, Janet L Stanford, Neil O'Callaghan and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

14 authors.

Liesel M FitzGerald *Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia. liesel.fitzgerald@utas.edu.au.
Chol-Hee Jung *Melbourne Bioinformatics, University of Melbourne, Parkville, VIC, Australia.
Ee Ming WongPrecision Medicine, School of Clinical Sciences at Monash Health Medicine, Nursing and Health Sciences, Monash University, Clayton, VIC, Australia.
JiHoon E JooCentre for Epidemiology and Biostatistics, School of Global and Population Health, University of Melbourne, Parkville, Australia.
Julie K BassettCancer Epidemiology Division, Cancer Council Victoria, Melbourne, VIC, Australia.
James G DowtyCentre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
Xiaoyu WangDivision of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA, USA.
James Y DaiDivision of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Janet L StanfordDivision of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Neil O'CallaghanPrecision Medicine, School of Clinical Sciences at Monash Health Medicine, Nursing and Health Sciences, Monash University, Clayton, VIC, Australia.
Tim NottleTissuPath, Mount Waverley, Melbourne, VIC, Australia.
John PedersenTissuPath, Mount Waverley, Melbourne, VIC, Australia.
Graham G GilesPrecision Medicine, School of Clinical Sciences at Monash Health Medicine, Nursing and Health Sciences, Monash University, Clayton, VIC, Australia.
Melissa C SoutheyPrecision Medicine, School of Clinical Sciences at Monash Health Medicine, Nursing and Health Sciences, Monash University, Clayton, VIC, Australia.

Funding

PROSTATE CANCER IN RELATION TO VASECTOMYR01CA056678 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI STANFORD, JANET L · 1993 to 1997
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Cure Cancer Australia/Prostate Cancer Foundation of Australia Young Investigators Grant YI 1812NCI NIH HHS R01 CA056678NHMRC Senior Research Fellowship 1061177
6 · The paper itself

Abstract

Differentially methylated CpG sites (dmCpGs) that distinguish prostate tumour from adjacent benign tissue could aid in the diagnosis and prognosis of prostate cancer. Previously, the identification of such dmCpGs has only been undertaken in radical prostatectomy (RP) samples and not primary diagnostic tumour samples (needle biopsy or transurethral resection of the prostate). We interrogated an Australian dataset comprising 125 tumour and 43 adjacent histologically benign diagnostic tissue samples, including 41 paired samples, using the Infinium Human Methylation450 BeadChip. Regression analyses of paired tumour and adjacent benign samples identified 2,386 significant dmCpGs (Bonferroni p < 0.01; delta-β ≥ 40%), with LASSO regression selecting 16 dmCpGs that distinguished tumour samples in the full Australian diagnostic dataset (AUC = 0.99). Results were validated in independent North American (n

Indexed as

CpG IslandsDNA MethylationProstatic NeoplasmsAgedAustraliaBiomarkers, TumorGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisProstatectomyBiomarkers, Tumor

Identifiers

PMID39095452
PMCPMC11297152

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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.