Regulation of uridine diphosphate-glucuronosyltransferase 1A expression by miRNA-214-5p and miRNA-486-3p

Author:

Paulusch Stefan1,Kalthoff Sandra1ORCID,Landerer Steffen1,Jansen Christian1,Schierwagen Robert2,Klein Sabine2,Trebicka Jonel2,Strassburg Christian P1

Affiliation:

1. Department of Internal Medicine I, University Hospital Bonn, Bonn 53127, Germany

2. Department of Internal Medicine I, University Hospital Frankfurt, Frankfurt 60590, Germany

Abstract

Aim: This study aimed to identify novel miRNAs (miRs) as regulators of UGT1A gene expression and to evaluate them as potential risk factors for the development of liver fibrosis/cirrhosis. Materials & methods: miRNA target sites in UDP-glucuronosyltransferase 1A (UGT1A) 3′-UTR were predicted and confirmed by luciferase assays, quantitative real-time PCR and western blot using HEK293, HepG2 and Huh7 cells. UGT1A and miRNA expression were analyzed in cirrhotic patients and a mouse model of alcoholic liver fibrosis. Results: miR-214-5p and miR-486-3p overexpression reduced UGT1A mRNA, protein levels and enzyme activity in HepG2 and Huh7 cells. miR-486-3p was upregulated in cirrhotic patients and fibrotic mice livers, whereas UGT1A mRNA levels were reduced. Conclusion: In conclusion, we identified two novel miRNAs capable to repress UGT1A expression in vitro and in vivo. Furthermore, miR-486-3p may represent a potential risk factor for the development or progression of liver fibrosis/cirrhosis by means of a reduced UGT1A-mediated detoxification activity.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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