Epigallocatechin-3-gallate Enhances the Efficacy of MicroRNA-34a Mimic  and MiR-93 Inhibitor Co-transfection in Prostate Cancer Cell Line

Hossein Mokhtari; Bahram Yaghmaei; Majid  Sirati-Sabet; Narjes Jafari; Alireza Mardomi; Saeid Abediankenari; Abdolkarim Mahrooz

doi:10.18502/ijaai.v19i6.4930

Hossein Mokhtari
Bahram Yaghmaei
Majid Sirati-Sabet
Narjes Jafari
Alireza Mardomi
Saeid Abediankenari
Abdolkarim Mahrooz

DOI: https://doi.org/10.18502/ijaai.v19i6.4930

Keywords: Androgen receptor; MicroRNAs; Prostate cancer; Prostate-specific antigen

Abstract

The potential role of microRNAs (miRNA) as therapeutic molecules has moved them from basic research to the field of cancer therapy. High expression of miR-93 and low expression of miR-34a have previously been indicated in prostate cancer (PC), which is the second leading cause of cancer-related death in men. Androgen receptor (AR) and prostate-specific antigen (PSA) play key roles in the initiation and progression of this cancer. Therefore, this study aimed to investigate the effects of the transfection and co-transfection of miR-34a mimic and miR-93 inhibitor with or without epigallocatechin-3-gallate (EGCG) on prostate cancer cell line and also to evaluate their effects on the expression of AR, PSA.

Human lymph node carcinoma of the prostate (LNCaP) cells were treated with miR-34a mimic or/and miR-93 inhibitor with or without EGCG. Gene or protein expressions were assessed by real-time PCR or western blotting of lysates.

The transfection with miR-34a mimics significantly reduced the mRNA expression of AR (p=0.0016), and PSA (p=0.038) compared to the control. Also, the miR-93 inhibitor led to a decrease in the mRNA expression of AR (p=0.0057) and PSA (p>0.05) compared to the control group. Furthermore, the co-transfection, along with EGCG, caused more decrease in both the AR (p<0.001) and the PSA (p=0.003) expression compared with the co-transfection without EGCG.

Our study indicates that the reduced expression of AR and PSA in PC cells followed by treatment with miR-34a mimic and miR-93 inhibitor and their combination with EGCG as a natural substance may be a promising therapeutic way for controlling the growth of these malignant cells.