TY - JOUR
T1 - miRNAs as molecular biomarkers for prostate cancer
AU - Coradduzza, Donatella
AU - Solinas, Tatiana
AU - Balzano, Francesca
AU - Culeddu, Nicola
AU - Rossi, Niccolò
AU - Cruciani, Sara
AU - Azara, Emanuela
AU - Maioli, Margherita
AU - Zinellu, Angelo
AU - De Miglio, Maria Rosaria
AU - Madonia, Massimo
AU - Falchi, Mario
AU - Carru, Ciriaco
PY - 2022/11/1
Y1 - 2022/11/1
N2 - miRNAs are short noncoding RNAs able to regulate specific mRNA stability, thus influencing target gene expression. Disrupted levels of several miRNAs have been associated with prostate cancer (PC), the leading cause of cancer death among men and the fifth leading cause of death worldwide. Herein, we investigated whether miR-145, miR-148, and miR-185 circulating levels in plasma could be used as molecular biomarkers, to allow distinguishing between individuals with benign prostatic hyperplasia, precancerous lesions, and PC. One-hundred and seventy urological clinic patients with suspected PC who underwent prostate biopsy were recruited. Total RNA was isolated from plasma, and TaqMan MicroRNA assays were used to analyze miR-145, miR-185, and miR-148 expression. First, differential miRNA expression among patient groups was evaluated. Then, miRNA levels were combined with clinical assessment outcomes, including results from invasive tests, using multivariate analysis to examine their ability in discriminating among the three patient groups. Our results suggest that miRNA is a promising molecular tool for clinical management of at-risk patients.
AB - miRNAs are short noncoding RNAs able to regulate specific mRNA stability, thus influencing target gene expression. Disrupted levels of several miRNAs have been associated with prostate cancer (PC), the leading cause of cancer death among men and the fifth leading cause of death worldwide. Herein, we investigated whether miR-145, miR-148, and miR-185 circulating levels in plasma could be used as molecular biomarkers, to allow distinguishing between individuals with benign prostatic hyperplasia, precancerous lesions, and PC. One-hundred and seventy urological clinic patients with suspected PC who underwent prostate biopsy were recruited. Total RNA was isolated from plasma, and TaqMan MicroRNA assays were used to analyze miR-145, miR-185, and miR-148 expression. First, differential miRNA expression among patient groups was evaluated. Then, miRNA levels were combined with clinical assessment outcomes, including results from invasive tests, using multivariate analysis to examine their ability in discriminating among the three patient groups. Our results suggest that miRNA is a promising molecular tool for clinical management of at-risk patients.
UR - http://www.scopus.com/inward/record.url?scp=85138715223&partnerID=8YFLogxK
U2 - 10.1016/j.jmoldx.2022.05.005
DO - 10.1016/j.jmoldx.2022.05.005
M3 - Article
SN - 1525-1578
VL - 24
SP - 1171
EP - 1180
JO - JOURNAL OF MOLECULAR DIAGNOSTICS
JF - JOURNAL OF MOLECULAR DIAGNOSTICS
IS - 11
ER -