miRNAs in the Box: Potential Diagnostic Role for Extracellular Vesicle-Packaged miRNA-27a and miRNA-128 in Breast Cancer

Author:

Giordano Cinzia123,Accattatis Felice Maria12,Gelsomino Luca12,Del Console Piercarlo12,Győrffy Balázs45ORCID,Giuliano Mario6,Veneziani Bianca Maria7ORCID,Arpino Grazia6ORCID,De Angelis Carmine6,De Placido Pietro6,Pietroluongo Erica6,Zinno Francesco8,Bonofiglio Daniela12ORCID,Andò Sebastiano12,Barone Ines12ORCID,Catalano Stefania123

Affiliation:

1. Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, Via P. Bucci, Arcavacata di Rende (CS), 87036 Cosenza, Italy

2. Centro Sanitario, University of Calabria, Via P. Bucci, Arcavacata di Rende (CS), 87036 Cosenza, Italy

3. Clinical Laboratory Unit, A.O. “Annunziata”, 87100 Cosenza, Italy

4. Departments of Bioinformatics and Pediatrics, Semmelweis University, 1094 Budapest, Hungary

5. TTK Cancer Biomarker Research Group, 1117 Budapest, Hungary

6. Department of Clinical Medicine and Surgery, University of Naples Federico II, 80133 Naples, Italy

7. Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80133 Naples, Italy

8. Immunohaematology and Transfusion Medicine, A.O. “Annunziata”, 87100 Cosenza, Italy

Abstract

Circulating extracellular vesicle (EV)-derived microRNAs (miRNAs) are now considered the next generation of cancer “theranostic” tools, with strong clinical relevance. Although their potential in breast cancer diagnosis has been widely reported, further studies are still required to address this challenging issue. The present study examined the expression profiles of EV-packaged miRNAs to identify novel miRNA signatures in breast cancer and verified their diagnostic accuracy. Circulating EVs were isolated from healthy controls and breast cancer patients and characterized following the MISEV 2018 guidelines. RNA-sequencing and real-time PCR showed that miRNA-27a and miRNA-128 were significantly down-regulated in patient-derived EVs compared to controls in screening and validation cohorts. Bioinformatics analyses of miRNA-target genes indicated several enriched biological processes/pathways related to breast cancer. Receiver operating characteristic (ROC) curves highlighted the ability of these EV-miRNAs to distinguish breast cancer patients from non-cancer controls. According to other reports, the levels of EV-miRNA-27a and EV-miRNA-128 are not associated with their circulating ones. Finally, evidence from the studies included in our systematic review underscores how the expression of these miRNAs in biofluids is still underinvestigated. Our findings unraveled the role of serum EV-derived miRNA-27a and miRNA-128 in breast cancer, encouraging further investigation of these two miRNAs within EVs towards improved breast cancer detection.

Funder

AIRC Investigator Grant

BANDO PRIN

National Research, Development and Innovation Office

Sistema Integrato di Laboratori per L’Ambiente

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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