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Updated: Jan 20, 2026

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Biomarker Potential of Plasma MicroRNA-150-5p in Prostate Cancer
Ionut Andrei Paunescu1,2, Razvan Bardan3,4, Anca Marcu5
1Department of Urology, Victor Babeș University of Medicine and Pharmacy, Timisoara 300041, Romania.
Abstract:
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.
Insights
This study identifies miR-150-5p as a potential non-invasive biomarker for prostate cancer (PCa). Plasma levels of miR-150-5p are significantly downregulated in PCa patients, correlating with tissue expression, suggesting its utility in early cancer detection.
Area of Science:
- Oncology
- Molecular Biology
- Biomarker Discovery
Background:
- Prostate cancer (PCa) is a leading cause of cancer mortality in men.
- MicroRNAs (miRNAs) are increasingly recognized as key players in PCa development and progression.
- miRNAs hold promise as novel, non-invasive biomarkers for cancer detection.
Purpose of the Study:
- To profile miRNA expression in plasma and tissues of PCa patients.
- To identify and validate candidate miRNAs as potential biomarkers for PCa.
- To investigate the correlation between plasma and tissue miRNA expression in PCa.
Main Methods:
- miRNA profiling was conducted on plasma and tissue samples from PCa patients.
- Candidate miRNAs showing dysregulation in both sample types were selected for validation.
- Quantitative real-time PCR and Receiver Operating Characteristic (ROC) analysis were used for validation and assessment of diagnostic accuracy.
Main Results:
- Five miRNAs (miR-130a-3p, miR-145-5p, miR-148a-3p, miR-150-5p, miR-365a-3p) were commonly dysregulated.
- miR-150-5p was significantly downregulated in both plasma (fold change -2.697, p < 0.001) and tissue (fold change -1.693, p = 0.035) samples.
- Plasma and tissue ROC analyses yielded AUCs of 0.817 and 0.809, respectively, indicating good diagnostic potential.
Conclusions:
- Plasma miR-150-5p levels correlate with prostate cancer tissue expression, suggesting its potential as a non-invasive biomarker.
- The findings support miR-150-5p as a promising candidate for PCa detection and monitoring.
- Further large-scale studies are warranted to confirm the diagnostic utility and biological role of miR-150-5p in PCa.
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