Abstract
BackgroundPrognostic biomarkers for localized prostate cancer (PCa) could improve personalized medicine. Our group previously identified a panel of differentially methylated CpGs in primary tumor tissue that predict disease aggressiveness, and here we further validate these biomarkers.
MethodsPyrosequencing was used to assess CpG methylation of eight biomarkers previously identified using the HumanMethylation450 array; CpGs with strongly correlated (r>0.70) results were considered technically validated. Logistic regression incorporating the validated CpGs and Gleason sum was used to define and lock a final model to stratify men with metastatic-lethal versus non-recurrent PCa in a training dataset. Coefficients from the final model were then used to construct a DNA methylation score, which was evaluated by logistic regression and Receiver Operating Characteristic (ROC) curve analyses in an independent testing dataset.
ResultsFive CpGs were technically validated and all were retained (P
ConclusionsThe DNA methylation score improved upon Gleason sum for predicting metastatic-lethal progression and holds promise for risk stratification of men with aggressive tumors. This prognostic score warrants further evaluation as a tool for improving patient outcomes.
Original language | English |
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Pages (from-to) | 1084-1091 |
Number of pages | 8 |
Journal | Prostate |
Volume | 78 |
Issue number | 14 |
DOIs | |
Publication status | Published - 1 Oct 2018 |
Keywords
- biomarker validation
- DNA methylation score
- metastatic-lethal
- prognostic
- prostate cancer
- GENE-EXPRESSION
- RISK
- BIOMARKERS
- CLASSIFIER