Abstract

MicroRNAs are involved in various pathologies including cancer. The aim of the study was to assess the level of expression of miR-96-5p, -134-5p, -181b-5p, -200b-3p in FFPE samples of prostate cancer, adjacent cancer-free tissue, and benign prostatic hyperplasia. Samples of 23 FFPE prostate cancer and 22 benign prostatic hyperplasias were dissected and HE stained. Compartments of tumor tissue and adjacent healthy glandular tissue were isolated from each sample using Laser Capture Microdissection. Total RNA was isolated from dissected tissues. Expression of miR-96-5p, miR-134-5p, 181b-5p, and miR-200b-3p was determined by real-time RT-qPCR method. The expression of miR-200b-3p was significantly higher in cancerous prostate: both in adenocarcinomatous glands and in the adjacent, apparently unaffected glands compared to BPH samples. The expression of miR-181b-5p was lower in in both prostate cancer tissues and adjacent tissue compared to BPH samples. Expression of miR-96-5p and miR-134-5p was lower in prostate cancer tissues compared to BPH. Levels of miR-96-5p, miR-134-5p, and 181b-5p negatively correlated with the Gleason score. Given further studies, miR-96-5p, miR-134-5p and especially miR-200b-3p and miR-181b-5p may differentiate BPH and PC.

Highlights

  • Prostate cancer (PC) is classified as an adenocarcinoma in over 95% cases and preferably locates in the peripheral region of the prostate gland (Oh 2003)

  • We found that the microRNA expression profile of benign prostatic hyperplasia (BPH) differs from PC (Fig. 2)

  • In PC the expression of miR-96-5p and miR-134-5p was downregulated compared to BPH. miR181b-5p was downregulated 93 times in PC and 19 times in adjacent tissue samples compared to BPH samples (p < 0.0001 and p = 0.0014, respectively)

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Summary

Introduction

Prostate cancer (PC) is classified as an adenocarcinoma in over 95% cases and preferably locates in the peripheral region of the prostate gland (Oh 2003). To lung cancer PC is responsible for the largest number of deaths. It is characterized by a relative high 5-year survival (98%), mainly due to frequent over diagnosis (Siegel et al 2019). PC over diagnosis is one of the major problems of clinical medicine, that leads to the unnecessary therapy of indolent cancers (Lomas and Ahmed 2020; Costello 2020). In 1966, Donald Gleason proposed histopathological grading scale for prostatic adenocarcinoma (Gleason 1966). It assesses dominant morphology and the second most common pattern (Oh 2003). It is broadly used as it correlates with prognosis and staging and as well as guides further therapy

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