Alterations of miRNA Expression in Diffuse Hyperplastic Perilobar Nephroblastomatosis: Mapping the Way to Understanding Wilms’ Tumor Development and Differential Diagnosis

Author:

Csók Ádám1ORCID,Micsik Tamás2,Magyar Zsófia3,Tornóczky Tamás4,Kuthi Levente5,Nishi Yumika1,Szirák Krisztina1,Csóka Monika6,Ottóffy Gábor7ORCID,Soltész Beáta1ORCID,Balogh István18ORCID,Buglyó Gergely1ORCID

Affiliation:

1. Department of Human Genetics, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

2. Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary

3. Department of Obstetrics and Gynaecology, Baross Street Division, Semmelweis University, 1088 Budapest, Hungary

4. Department of Pathology, University of Pécs Medical School and Clinical Center, 7624 Pécs, Hungary

5. Department of Pathology, Faculty of Medicine, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary

6. Department of Paediatrics, Semmelweis University, 1094 Budapest, Hungary

7. Department of Pediatrics, University of Pécs Medical School and Clinical Center, 7623 Pécs, Hungary

8. Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

Abstract

Wilms’ tumor (WT) is the most common renal malignancy in children. In diffuse hyperplastic perilobar nephroblastomatosis (DHPLN), nephrogenic rests result in a bulky enlargement of the kidney, a condition considered as a premalignant state before WT. Despite relevant clinical differences between WT and DHPLN, they are often challenging to distinguish based on histology. Molecular markers would improve differential diagnosis, but none are available at present. In our study, we investigated the potential of microRNAs (miRNAs) as such biomarkers, also aiming to shed light on the chronological order of expression changes. Formalin-fixed, paraffin-embedded (FFPE) samples from four DHPLN cases and adjacent healthy tissues were tested using a PCR array containing primers for 84 miRNAs implicated in genitourinary cancer. Expression in DHPLN was compared to WT data available in dbDEMC. Let-7, miR-135, miR-146a-5p, miR-182-5p, miR-183-5p, miR-20b-3p, miR-29b-3p, miR-195-5p and miR-17-5p showed potential to be used as biomarkers to distinguish WT and DHPLN in cases when traditional differential diagnosis is inconclusive. Our study also revealed miRNAs which may play a role in the initial steps of the pathogenesis (at a precancerous stage) and ones which become deregulated later in WT. More experiments are needed to confirm our observations and find new candidate markers.

Publisher

MDPI AG

Subject

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

Reference51 articles.

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5. Hereditary renal tumor syndromes;Kuthi;Orv. Hetil.,2023

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