Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/3632
Title: Association of KLK3, VAMP8 and MDM4 Genetic Variants within microRNA Binding Sites with Prostate Cancer: Evidence from Serbian Population
Authors: Kotarac, Nevena 
Dobrijevic, Zorana
Matijašević, Suzana 
Savić-Pavićević, Dušanka 
Brajušković, Goran 
Keywords: Prostate cancer;miRSNPs;rs1010;rs1058205;rs4245739
Issue Date: Jun-2020
Rank: M22
Journal: Pathology & Oncology Research
Series/Report no.: 26(4);2409-23
Abstract: 
A growing number of studies have suggested that genetic variants affecting the micro-RNA- binding mechanisms (miRSNPs) constitute a promising novel class of biomarkers for prostate cancer (PCa) biology. Among the most extensively studied miRSNPs in the context of cancer is the variation rs4245739 in the MDM4 gene, while a recent large-scale analysis revealed significant differences in genotype distributions between aggressive and non-aggressive disease for rs1058205 in KLK3 and rs1010 in VAMP8. In this study, we examined a total of 1083 subjects for these three variants using Taqman® SNP Genotyping Assays. Three hundred and fifty-five samples of peripheral blood were obtained from patients with PCa and 358 samples from patients with benign prostatic hyperplasia (BPH). The control group consisted of 370 healthy volunteers. Comparisons of genotype distributions among PCa and BPH patients, as well as between PCa patients and healthy controls, yielded no evidence of association between the analyzed genetic variants and the risk of developing PCa. However, all three tested genetic variants have shown the association with the parameters of PCa progression. For KLK3 variant rs1058205, minor allele C was found to associate with the lower serum PSA score in PCa patients (PSA > 20 ng/ml vs. PSA < 10 ng/ml comparison, Prec = 0.038; ORrec = 0.20, 95%CI 0.04-1.05). The obtained results point out the potential relevance of the tested genetic variants for the disease aggressiveness assessment.
URI: https://biore.bio.bg.ac.rs/handle/123456789/3632
ISSN: 1219-4956
1532-2807
DOI: 10.1007/s12253-020-00839-7
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