Journal article
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, Tim Nottle, John Pedersen, Graham G Giles, Melissa C Southey
Scientific Reports | Nature Portfolio | Published : 2024
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..
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Grants
Awarded by Cure Cancer Australia/Prostate Cancer Foundation of Australia Young Investigators Grant
Awarded by NCI NIH HHS
Awarded by NHMRC Senior Research Fellowship