| Literature DB >> 33922968 |
Irena Abramovic1,2,3, Borna Vrhovec4, Lucija Skara1,2,3, Alen Vrtaric3,5, Nora Nikolac Gabaj3,5,6, Tomislav Kulis2,3,7, Goran Stimac2,4, Dejan Ljiljak8, Boris Ruzic2,3,4, Zeljko Kastelan2,3,7, Bozo Kruslin3,9, Floriana Bulic-Jakus1,2,3, Monika Ulamec2,3,9,10, Ana Katusic-Bojanac1,3, Nino Sincic1,2,3.
Abstract
Prostate cancer (PCa) is the most commonly diagnosed neoplasm among men. Since it often resembles benign prostate hyperplasia (BPH), biomarkers with a higher differential value than PSA are required. Epigenetic biomarkers in liquid biopsies, especially miRNA, could address this challenge. The absolute expression of miR-375-3p, miR-182-5p, miR-21-5p, and miR-148a-3p were quantified in blood plasma and seminal plasma of 65 PCa and 58 BPH patients by digital droplet PCR. The sensitivity and specificity of these microRNAs were determined using ROC curve analysis. The higher expression of miR-182-5p and miR-375-3p in the blood plasma of PCa patients was statistically significant as compared to BPH (p = 0.0363 and 0.0226, respectively). Their combination achieved a specificity of 90.2% for predicting positive or negative biopsy results, while PSA cut-off of 4 µg/L performed with only 1.7% specificity. In seminal plasma, miR-375-3p, miR-182-5p, and miR-21-5p showed a statistically significantly higher expression in PCa patients with PSA >10 µg/L compared to ones with PSA ≤10 µg/L. MiR-182-5p and miR-375-3p in blood plasma show higher performance than PSA in discriminating PCa from BPH. Seminal plasma requires further investigation as it represents an obvious source for PCa biomarker identification.Entities:
Keywords: benign prostate hyperplasia; biomarkers; liquid biopsy; microRNA; plasma; prostate cancer; seminal fluid
Year: 2021 PMID: 33922968 DOI: 10.3390/cancers13092068
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639