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DNA Methylation Screening of Primary Prostate Tumors Identifies SRD5A2 and CYP11A1 as Candidate Markers for Assessing Risk of Biochemical Recurrence
University of Texas Health Science Center, San Antonio, USA.
Högskolan i Skövde, Institutionen för biovetenskap. Högskolan i Skövde, Forskningscentrum för Systembiologi. Manitoba Institute of Cell Biology, University of Manitoba, Winnipeg, Manitoba, Canada / Department of Clinical Genetics, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. (Tumörbiologi, Tumor Biology)ORCID-id: 0000-0002-4524-0783
University of Texas Health Science Center, San Antonio, USA.
University of Texas Health Science Center, San Antonio, USA.
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2015 (Engelska)Ingår i: The Prostate, ISSN 0270-4137, E-ISSN 1097-0045, Vol. 75, nr 15, s. 1790-1801Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

BACKGROUND. Altered DNA methylation in CpG islands of gene promoters has been implicated in prostate cancer (PCa) progression and can be used to predict disease outcome. In this study, we determine whether methylation changes of androgen biosynthesis pathway (ABP)-related genes in patients' plasma cell-free DNA (cfDNA) can serve as prognostic markers for biochemical recurrence (BCR). METHODS. Methyl-binding domain capture sequencing (MBDCap-seq) was used to identify differentially methylated regions (DMRs) in primary tumors of patients who subsequently developed BCR or not, respectively. Methylation pyrosequencing of candidate loci was validated in cfDNA samples of 86 PCa patients taken at and/or post-radical prostatectomy (RP) using univariate and multivariate prediction analyses. RESULTS. Putative DMRs in 13 of 30 ABP-related genes were found between tumors of BCR (n = 12) versus no evidence of disease (NED) (n = 15). In silico analysis of The Cancer Genome Atlas data confirmed increased DNA methylation of two loci-SRD5A2 and CYP11A1, which also correlated with their decreased expression, in tumors with subsequent BCR development. Their aberrant cfDNA methylation was also associated with detectable levels of PSA taken after patients' post-RP. Multivariate analysis of the change in cfDNA methylation at all of CpG sites measured along with patient's treatment history predicted if a patient will develop BCR with 77.5% overall accuracy. CONCLUSIONS. Overall, increased DNA methylation of SRD5A2 and CYP11A1 related to androgen biosynthesis functions may play a role in BCR after patients' RP. The correlation between aberrant cfDNA methylation and detectable PSA in post-RP further suggests their utility as predictive markers for PCa recurrence. (C) 2015 Wiley Periodicals, Inc.

Ort, förlag, år, upplaga, sidor
Wiley-Blackwell, 2015. Vol. 75, nr 15, s. 1790-1801
Nyckelord [en]
prostate cancer, DNA methylation, plasma, biochemical recurrence
Nationell ämneskategori
Medicinsk genetik Cancer och onkologi Urologi och njurmedicin
Identifikatorer
URN: urn:nbn:se:his:diva-13580DOI: 10.1002/pros.23052ISI: 000363219200013PubMedID: 26332453Scopus ID: 2-s2.0-84942830759OAI: oai:DiVA.org:his-13580DiVA, id: diva2:1098036
Tillgänglig från: 2017-05-23 Skapad: 2017-05-23 Senast uppdaterad: 2019-02-19Bibliografiskt granskad

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Awe, Julius AdebayoJadhav, Rohit R.Mai, Sabine

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Awe, Julius AdebayoJadhav, Rohit R.Mai, Sabine
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Institutionen för biovetenskapForskningscentrum för Systembiologi
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The Prostate
Medicinsk genetikCancer och onkologiUrologi och njurmedicin

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