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Article

Biomarker Potential of Plasma MicroRNA-150-5p in Prostate Cancer

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Department of Urology, Victor Babeș University of Medicine and Pharmacy, Timisoara 300041, Romania
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Urology Clinic, Timisoara Emergency County Hospital, Timisoara 300723, Romania
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Department of Biochemistry & Pharmacology, Victor Babes University of Medicine and Pharmacy, Timisoara 300041, Romania
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Department of Pathology, “Victor Babeş” University of Medicine and Pharmacy, Timisoara 300041, Romania
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Department of Oncology, “Victor Babeş” University of Medicine and Pharmacy, Timisoara 300041, Romania
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Department of Functional Genomics, Proteomics and Experimental Pathology, The Oncology Institute “Prof. Dr. Ion Chiricuta”, Cluj-Napoca 400015, Romania
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Department of Urology, The Oncology Institute “Prof. Dr. Ion Chiricuta”, Cluj-Napoca 400015, Romania
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Authors to whom correspondence should be addressed.
Medicina 2019, 55(9), 564; https://doi.org/10.3390/medicina55090564
Received: 15 July 2019 / Revised: 29 August 2019 / Accepted: 30 August 2019 / Published: 3 September 2019
Background and Objectives: Over decades, prostate cancer (PCa) has become one of the leading causes of cancer mortality in men. Extensive evidence exists that microRNAs (miRNAs or miRs) are key players in PCa and a new class of non-invasive cancer biomarkers. Materials and Methods: We performed miRNA profiling in plasma and tissues of PCa patients and attempted the validation of candidate individual miRs as biomarkers. Results: The comparison of tissue and plasma profiling results revealed five commonly dysregulated miRs, namely, miR-130a-3p, miR-145-5p, miR-148a-3p, miR-150-5p, and miR-365a-3p, of which only three show concordant changes—miR-130a-3p and miR-150-5p were downregulated and miR-148a-3p was upregulated in both tissue and plasma samples, respectively. MiR-150-5p was validated as significantly downregulated in both plasma and tissue cancer samples, with a fold change of −2.697 (p < 0.001), and −1.693 (p = 0.035), respectively. ROC analysis showed an area under the curve (AUC) of 0.817 (95% CI: 0.680–0.995) for plasma samples and 0.809 (95% CI: 0.616–1.001) for tissue samples. Conclusions: We provide data indicating that miR-150-5p plasma variations in PCa patients are associated with concordant changes in prostate cancer tissues; however, given the heterogeneous nature of previous findings of miR-150-5p expression in PCa cells, additional future studies of a larger sample size are warranted in order to confirm the biomarker potential and role of miRNA-150-5p in PCa biology. View Full-Text
Keywords: prostate cancer; microRNA-150-5p; biomarkers; plasma prostate cancer; microRNA-150-5p; biomarkers; plasma
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MDPI and ACS Style

Paunescu, I.A.; Bardan, R.; Marcu, A.; Nitusca, D.; Dema, A.; Negru, S.; Balacescu, O.; Balacescu, L.; Cumpanas, A.; Sirbu, I.O.; Petrut, B.; Seclaman, E.; Marian, C. Biomarker Potential of Plasma MicroRNA-150-5p in Prostate Cancer. Medicina 2019, 55, 564. https://doi.org/10.3390/medicina55090564

AMA Style

Paunescu IA, Bardan R, Marcu A, Nitusca D, Dema A, Negru S, Balacescu O, Balacescu L, Cumpanas A, Sirbu IO, Petrut B, Seclaman E, Marian C. Biomarker Potential of Plasma MicroRNA-150-5p in Prostate Cancer. Medicina. 2019; 55(9):564. https://doi.org/10.3390/medicina55090564

Chicago/Turabian Style

Paunescu, Ionut A., Razvan Bardan, Anca Marcu, Diana Nitusca, Alis Dema, Serban Negru, Ovidiu Balacescu, Loredana Balacescu, Alin Cumpanas, Ioan O. Sirbu, Bogdan Petrut, Edward Seclaman, and Catalin Marian. 2019. "Biomarker Potential of Plasma MicroRNA-150-5p in Prostate Cancer" Medicina 55, no. 9: 564. https://doi.org/10.3390/medicina55090564

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