Urine Cell-Free MicroRNAs in Localized Prostate Cancer Patients.

Abstract

Simple SummaryUrine cell-free microRNAs (cfmiRs) are promising biomarkers for the detection of prostate cancer (PCa) and may replace or complement prostate-specific antigen screening. This pilot study aims to demonstrate the diagnostic utility of urine cfmiRs for early-stage PCa using a robust microRNA (miR) panel based on next-generation sequencing. We assessed urine, plasma, and formalin-fixed paraffin-embedded tumor tissue samples obtained from patients diagnosed with pT2 PCa. Differentially expressed miRs were found in urine, plasma, and tumor samples obtained from PCa patients. Through bioinformatic analysis, several miRs were found as potential cfmiRs with utility for the detection of PCa. Our results showed that specific cfmiRs in urine samples from PCa patients may have potential utility in the detection of early-stage PCa.Prostate cancer (PCa) is the most common cancer in men. Prostate-specific antigen screening is recommended for the detection of PCa. However, its specificity is limited. Thus, there is a need to find more reliable biomarkers that allow non-invasive screening for early-stage PCa. This study aims to explore urine microRNAs (miRs) as diagnostic biomarkers for PCa. We assessed cell-free miR (cfmiR) profiles of urine and plasma samples from pre- and post-operative PCa patients (n = 11) and normal healthy donors (16 urine and 24 plasma) using HTG EdgeSeq miRNA Whole Transcriptome Assay based on next-generation sequencing. Furthermore, tumor-related miRs were detected in formalin-fixed paraffin-embedded tumor tissues obtained from patients with localized PCa. Specific cfmiRs signatures were found in urine samples of localized PCa patients using differential expression analysis. Forty-two cfmiRs that were detected were common to urine, plasma, and tumor samples. These urine cfmiRs may have potential utility in diagnosing early-stage PCa and complementing or improving currently available PCa screening assays. Future studies may validate the findings.