Abstract

The term liquid biopsy reveals a non-invasive diagnostic method that might be based on the quantification of cell-free microRNAs in body fluids. However, the identification of candidates for liquid biopsy is challenging. Our aim was to compare the cell-free expression of miR-483-5p, miR-205-5p, and let-7f-5p in ovarian cell cultures and plasma samples of patients with ovarian cancer. Both the intracellular and cell-free expression of miR-205-5p and let-7f-5p proved to be higher in the Estrogen Receptor α (ERα) expressing PEO1 cell-line than in the estrogen non-sensitive A2780. Moreover, the expression of let-7f-5p was up-regulated in response to estradiol exposure that was diminished after the addition of an ERα selective antagonist. MiR-483-5p had lower intracellular and cell-free expression in PEO1. All these miRNAs had detectable expression level in plasma samples, among which miR-205-5p proved to be overexpressed in the plasma samples of patients with ovarian tumors compared to healthy controls and possessed an acceptable diagnostic potential with ROC-AUC 0.683 (95% CI 0.57–0.795). Functional annotation clustering of the target genes of miR-205-5p revealed several clusters involved in cancer development. We suggest that miR-205-5p might be a promising biomarker candidate in ovarian cancer that should be further analyzed in larger sample size.

Highlights

  • The Basal Expression of miR-205-5p and let-7f-5p Is Higher in the Estrogen Sensitive PEO1

  • In the beginning of our work, the basal expression level of miR-483-5p, miR-205-5p, and let-7f-5p was determined in epithelial ovarian cell lines

  • We applied two cell lines that differed in the expression of Estrogen Receptor α (ERα); that receptor highly determined the expression of miRNAs in our previous studies [11]

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Liquid biopsy is a promising non-invasive diagnostic approach that is based on the quantification of biomarkers in body fluids and has several advantages over conventional tissue biopsies [1,2]. Cell-free counterparts of nucleic acids are considered to be applicable biomarker candidates for liquid biopsy. These include different types of cell-free DNA (e.g., genomic DNA or mitochondrial DNA fragments) and non-coding RNA molecules (e.g., microRNAs, circular RNAs, long non-coding RNAs) [1]. Among non-coding RNA molecules, most studies focus on miRNAs due to the following reasons: (i) they are stable;

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