Epigenomic profiling of prostate cancer identifies differentially methylated genes in TMPRSS2:ERG fusion-positive versus fusion-negative tumors

Autor: Joshi J. Alumkal, Piet A. van den Brandt, Manuel Luedeke, Jian-Bing Fan, Irene M. Shui, Marina Bibikova, Janet L. Stanford, Brandy Klotzle, Ziding Feng, Milan S. Geybels, Christiane Maier, Elaine A. Ostrander, Antje E. Rinckleb, Shanshan Zhao
Přispěvatelé: Epidemiologie, RS: CAPHRI School for Public Health and Primary Care, RS: CAPHRI - R3 - Functioning, Participating and Rehabilitation, RS: CAPHRI - R5 - Optimising Patient Care, RS: GROW - Oncology, RS: GROW - R1 - Prevention
Jazyk: angličtina
Rok vydání: 2015
Předmět:
Zdroj: Clinical epigenetics, 7:128. BioMed Central Ltd
Clinical Epigenetics
ISSN: 1868-7083
Popis: Background About half of all prostate cancers harbor the TMPRSS2:ERG (T2E) gene fusion. While T2E-positive and T2E-negative tumors represent specific molecular subtypes of prostate cancer (PCa), previous studies have not yet comprehensively investigated how these tumor subtypes differ at the epigenetic level. We therefore investigated epigenome-wide DNA methylation profiles of PCa stratified by T2E status. Results The study included 496 patients with clinically localized PCa who had a radical prostatectomy as primary treatment for PCa. Fluorescence in situ hybridization (FISH) “break-apart” assays were used to determine tumor T2E-fusion status, which showed that 266 patients (53.6 %) had T2E-positive PCa. The study showed global DNA methylation differences between tumor subtypes. A large number of differentially methylated CpG sites were identified (false-discovery rate [FDR] Q-value
Databáze: OpenAIRE