Title Urinary DNA methylation biomarkers for prediction of prostate cancer upgrading and upstaging /
Authors Bakavičius, Arnas ; Daniūnaitė, Kristina ; Žukauskaitė, Kristina ; Barisienė, Marija ; Jarmalaitė, Sonata ; Jankevičius, Feliksas
DOI 10.1186/s13148-019-0716-z
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Is Part of Clinical epigenetics.. BioMed Central Ltd.. 2019, vol. 11, iss. 1, art. no. 115, p. [1-10].. ISSN 1868-7075. eISSN 1868-7083
Keywords [eng] DNA methylation ; Prostate cancer ; Upgrading ; Upstaging ; Urine
Abstract [eng] Background: Significant numbers of prostate cancer (PCa) patients experience tumour upstaging and upgrading in surgical specimens that cause serious problems in timely and proper selection of the treatment strategy. This study was aimed at the evaluation of a set of established epigenetic biomarkers as a noninvasive tool for more accurate PCa categorization before radical prostatectomy (RP). Methods: Quantitative methylation-specific PCR was applied for the methylation analysis of RARB, RASSF1, and GSTP1 in 514 preoperatively collected voided or catheterized urine samples from the single-centre cohort of 1056 treatment-naïve PCa patients who underwent RP. The rates of biopsy upgrading and upstaging were analysed in the whole cohort. Results: Pathological examination of RP specimens revealed Gleason score upgrading in 27.2% and upstaging in 20.3% of the patients with a total misclassification rate of 39.0%. DNA methylation changes in at least one gene were detected in more than 80% of urine samples. Combination of the PSA test with the three-gene methylation analysis in urine was a significant predictor of pathological upstaging and upgrading (P < 0.050), however, with limited increase in overall accuracy. The PSA test or each gene alone was not informative enough. Conclusions: The urinary DNA methylation assay in combination with serum PSA may predict tumour stage or grade migration post-RP aiding in improved individual risk assessment and appropriate treatment selection. Clinical utility of these biomarkers should be proven in larger multi-centre studies.
Published BioMed Central Ltd
Type Journal article
Language English
Publication date 2019
CC license CC license description