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BACKGROUND: Prostate cancer (PCa) remains the leading cause of cancer deaths in men. The prostate-specific antigen (PSA) test is widely used for PCa screening, but it lacks specificity and can lead to over-diagnosis and over-treatment. New, effective and affordable markers are therefore needed. RESULTS: Using enzymatic methyl sequencing (EM-Seq), methylation-specific PCR (MS-PCR), and transcriptomics including a spatial approach, we analyzed tumor and non-tumor samples from radical prostatectomy specimens. Comprehensive methylome was performed in 15 paired samples of prostate cancer and their adjacent non-tumor tissue by EM-Seq. From over 4-million differentially methylated CpG sites, we identified 66 CpGs sites representing eight genes: CLDN5, GSTP1, NBEAL2, PRICKLE2, SALL3, TAMALIN/GRASP, TJP2, and TMEM106A which were hypermethylated in PCa tissues (p-value 

Original publication

DOI

10.1186/s13148-025-01930-z

Type

Journal article

Journal

Clin Epigenetics

Publication Date

11/07/2025

Volume

17

Keywords

Epigenetic DNA markers, Methylation-specific PCR, Methylome sequencing, Prostate cancer, Humans, Male, Prostatic Neoplasms, DNA Methylation, CpG Islands, Biomarkers, Tumor, Epigenesis, Genetic, Aged, Middle Aged, Gene Expression Profiling, Sequence Analysis, DNA, Gene Expression Regulation, Neoplastic, Prostatectomy