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. 2019 May 25;20(5):1453-1456.
doi: 10.31557/APJCP.2019.20.5.1453.

Circulating miR-20a and miR-26a as Biomarkers in Prostate Cancer

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Circulating miR-20a and miR-26a as Biomarkers in Prostate Cancer

Peyman Mohammadi Torbati et al. Asian Pac J Cancer Prev. .

Abstract

Objective: Circulating microRNAs (miRNAs), present in body fluids, have been considering importance as cancer biomarkers. The primary aim of this study was to assess whether circulatory miR-20a and miR-26a can be used as diagnostic biomarkers in prostate cancer (PCa). Methods: Relative expression miR-20a and miR-26a has been assessed in 40 patients with PCa and 40 non-cancerous volunteer. Sample Collection of patients was performed before and one week after prostatectomy. Total RNA was extracted from serum and miR-20a and miR-26a expressions were quantified by using Real-Time PCR method. Results: miR-20a was significantly up-regulated in pre-operation serum samples of PCa patients compared to the serum samples of non-cancerous controls, however, in post-operation samples no significant differences was showed. miR-26a level was not significantly decreased in pre and post-operation serum samples compared to the serum samples of controls. However, the expression level ratios of both miR-20a and miR-26a were insignificantly decreased when post-operation serum samples compared to pre-operation ones. Conclusion: Decrement of circulating miR-20a and miR-26a in patients after surgery may reflect the tumoral origin of those microRNAs and the results may use for tumor remnant monitoring after prostatectomy.

Keywords: Prostate cancer; circulatory microRNAs; miR-20a; miR-26a.

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Figures

Figure 1
Figure 1
Relative Expression of Circulating miR-20a and miR-26a. Post-O and Pre-O, post-operation and pre-operation serum samples, respectively; ns, non-significant; *, p-value < 0.05; **, p-value < 0.01; ***, p-value < 0.001.

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References

    1. Ambs S, Prueitt RL, Yi M, et al. Genomic profiling of microRNA and messenger RNA reveals deregulated microRNA expression in prostate cancer. Cancer Res. 2008;68:6162–70. - PMC - PubMed
    1. Backer H. Prostate cancer screening:exploring the debate. Permanente J. 1999;3:330–40.
    1. Brase JC, Johannes M, Schlomm T, et al. Circulating miRNAs are correlated with tumor progression in prostate cancer. Int J Cancer. 2011;128:608–16. - PubMed
    1. Bryant R, Pawlowski T, Catto J, et al. Changes in circulating microRNA levels associated with prostate cancer. Br J Cancer. 2012;106:768. - PMC - PubMed
    1. Deng M, Tang H-l, Lu X-h, et al. miR-26a suppresses tumor growth and metastasis by targeting FGF9 in gastric cancer. PLoS One. 2013;8:e72662. - PMC - PubMed