Author/Authors :
Emamvirdizadeh ، Alireza Department of Genetics - Faculty of Advanced Science and Technology - Islamic Azad University , Jamshidian ، Faranak Department of Biology - Faculty of Basic Sciences - Islamic Azad University, East Tehran Branch (Ghiamdasht) , Entezari ، Maliheh Department of Genetics - Faculty of Advanced Science and Technology - Islamic Azad University , Nooraei ، Saghi Department of Genetics - Faculty of Advanced Science and Technology - Islamic Azad University , Hashemi ، Mehrdad Department of Genetics - Faculty of Advanced Science and Technology - Islamic Azad University
Abstract :
Background: Prostate cancer is the most prevalent cancer amongmenworldwide. Diagnosis in this cancer is primarily done, using aggressive methods such as biopsy. Laboratory methods, such as the measurement of prostate-specific antigen (PSA) in the blood, do not have high sensitivity and specificity. MicroRNAs (miRNAs), a group of diagnostic biomarkers, can diagnose diseases such as cancer. MicroRNA (miRNA) is a small, non-coding, single-stranded RNA with a length of 21 to 23 nucleotides. Objectives: This study was designed to investigate the changes in the expression level of miR-21 and miR-214 in the urine of patients with prostate cancer compared with healthy controls. Methods: A total of 70 urine samples from prostate cancer patients (32 metastatic and 38 non-metastatic) and 30 from healthy subjects with negative biopsy reports were collected. The expression level of miR-21 and miR-214 in the urine were detected by quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Results: miR-21 showed a significant increase in expression (P = 0.003) and miR-214 showed a significant decrease in expression (P = 0.000) compared with the control group. The specificity, sensitivity, and area under the curve (AUC) were 100, 72.14, and 0.721% for combined panels of miR-21 and miR-214 and 63.33, 61.43, and 0.620%, respectively, for PSA. Conclusions: miR-21 and miR-214 showed significant change in expression in patients with prostate cancer compared with healthy subjects. It is hoped that, with further research, a combined panel of miR-21 and miR-214 can be used as a non-invasive method for detecting prostate cancer with higher sensitivity and specificity than the PSA test.
