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miR-143 expression profiles in urinary bladder cancer: correlation with clinical and epidemiological parameters

Authors :
Soumaya Rammeh
Manuela Spagnuolo
Nouha Setti Boubaker
Ahlem Blel
Omar Karray
Ahmed Saadi
Rahma Said
Nesrine Trabelsi
Giulia Piaggio
Giulia Regazzo
Slah Ouerhani
Mohamed Chebil
Aymone Gurtner
Maria Giulia Rizzo
Haroun Ayed
Source :
Molecular Biology Reports. 47:1283-1292
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

Hsa-mir-143 and hsa-let-7c have been reported to be deregulated in multiple neoplasms. The main purpose of this study was to investigate the expression of these miRNAs in bladder cancer (BCa) and to analyze the association between their expression profiles and clinical and epidemiological parameters. Ninety BCa specimens were included. Expression patterns of miR-143 and let-7c were assessed by qRT-PCR using Taqman specific probes. Validated and predicted targets of these miRNA's were identified using CSmiRTar and DAVID tools, respectively. miR-143 was downregulated in tumors compared to controls (mean fold-change (FC) = 0.076). Its expression was significantly higher in MIBC compared to NMIBC (p = 0,001). Its value as a potential biomarker discriminating non invasive tumors from the invasive ones was confirmed by ROC curve (AUC = 0.768; p = 0.0001). Also, this down-regulation positively correlates with frequency of tobacco use (p = 0,04) and chronic alcohol consumption (p = 0,04). Let-7c was overexpressed in BCa samples (mean (FC = 9.92) compared to non tumoral ones but was not associated to clinical and epidemiological parameters. A comprehensive overview of miR-143 targets and pathways implicated in BCa initiation, diagnosis or prognosis using bioinformatical analysis, was conducted. While both deregulated miRNAs may contribute to urothelial tumorigenesis, the deregulation of miR-143 was significantly correlated to epidemiological and clinical parameters.

Details

ISSN :
15734978 and 03014851
Volume :
47
Database :
OpenAIRE
Journal :
Molecular Biology Reports
Accession number :
edsair.doi.dedup.....28d53f6fc83af59baca473fb277854be
Full Text :
https://doi.org/10.1007/s11033-019-05228-1