Role of miR-653 and miR-29c in downregulation of CYP1A2 expression in hepatocellular carcinoma
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
17-28231A
Ministerstvo Zdravotnictví Ceské Republiky
DRO (UHHK, 00179906)
Ministerstvo Zdravotnictví Ceské Republiky
RVO:68081707
Akademie Věd České Republiky
PubMed
34780054
DOI
10.1007/s43440-021-00338-9
PII: 10.1007/s43440-021-00338-9
Knihovny.cz E-zdroje
- Klíčová slova
- AHR, Biotransformation, CYP1A2, Hepatocellular carcinoma, microRNA,
- MeSH
- biotransformace MeSH
- cytochrom P-450 CYP1A2 metabolismus MeSH
- down regulace MeSH
- hepatocelulární karcinom * genetika metabolismus MeSH
- hepatocyty metabolismus MeSH
- lidé MeSH
- mikro RNA metabolismus MeSH
- nádorové buněčné linie MeSH
- nádory jater * genetika metabolismus MeSH
- regulace genové exprese u nádorů MeSH
- xenobiotika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- CYP1A2 protein, human MeSH Prohlížeč
- cytochrom P-450 CYP1A2 MeSH
- mikro RNA MeSH
- MIRN29C microRNA, human MeSH Prohlížeč
- MIRN653 microRNA, human MeSH Prohlížeč
- xenobiotika MeSH
BACKGROUND: Hepatocellular carcinoma (HCC) is a major contributor to the worldwide cancer burden. Recent studies on HCC have demonstrated dramatic alterations in expression of several cytochrome P450 (CYP) family members that play a crucial role in biotransformation of many drugs and other xenobiotics; however, the mechanisms responsible for their deregulation remain unclear. METHODS: We investigated a potential involvement of miRNAs in downregulation of expression of CYPs observed in HCC tumors. We compared miRNA expression profiles (TaqMan Array Human MicroRNA v3.0 TLDA qPCR) between HCC human patient tumors with strong (CYP-) and weak/no (CYP+) downregulation of drug-metabolizing CYPs. The role of significantly deregulated miRNAs in modulation of expression of the CYPs and associated xenobiotic receptors was then investigated in human liver HepaRG cells transfected with relevant miRNA mimics or inhibitors. RESULTS: We identified five differentially expressed miRNAs in CYP- versus CYP+ tumors, namely miR-29c, miR-125b1, miR-505, miR-653 and miR-675. The two most-upregulated miRNAs found in CYP- tumor samples, miR-29c and miR-653, were found to act as efficient suppressors of CYP1A2 or AHR expression. CONCLUSIONS: Our results revealed a novel role of miR-653 and miR-29c in regulation of expresion of CYPs involved in crucial biotransformation processes in liver, which are often deregulated during liver cancer progression.
Central European Institute of Technology Masaryk University Brno Czech Republic
Department of Biology Faculty of Medicine Masaryk University Brno Czech Republic
Department of Experimental Biology Faculty of Science Masaryk University Brno Czech Republic
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