Evidence map›Paper›PMID 34780054›Full record

ArticlePharmacological reports : PR2022

Role of miR-653 and miR-29c in downregulation of CYP1A2 expression in hepatocellular carcinoma.

Martin Krkoška, Jana Nekvindová, Kateřina Nevědělová, Veronika Zubáňová, Lenka Radová, Jan Vondráček, Jarmila Herůdková, Ondřej Slabý, Igor Kiss, Lucia Bohovicová and 7 more

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Article in Pharmacological reports : PR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 56% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 1 country.

Martin Krkoška *Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Královopolská 135, 612 65, Brno, Czech Republic.ORCID http://orcid.org/0000-0002-9306-9140
Jana Nekvindová *Institute of Clinical Biochemistry and Diagnostics, University Hospital Hradec Králové, Hradec Králové, Czech Republic.ORCID http://orcid.org/0000-0002-2861-5483
Kateřina NevědělováDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Královopolská 135, 612 65, Brno, Czech Republic.
Veronika ZubáňováInstitute of Clinical Biochemistry and Diagnostics, University Hospital Hradec Králové, Hradec Králové, Czech Republic.ORCID http://orcid.org/0000-0001-9193-0972
Lenka RadováCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.
Jan VondráčekDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Královopolská 135, 612 65, Brno, Czech Republic.ORCID http://orcid.org/0000-0003-4071-1969
Jarmila HerůdkováDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Královopolská 135, 612 65, Brno, Czech Republic.
Ondřej SlabýCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID http://orcid.org/0000-0002-8450-0584
Igor KissDepartment of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Lucia BohovicováDepartment of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Pavel FabianDepartment of Oncological and Experimental Pathology, Masaryk Memorial Cancer Institute, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Zuzana TylichováDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Královopolská 135, 612 65, Brno, Czech Republic.ORCID http://orcid.org/0000-0003-0433-5505
Zdeněk KalaDepartment of Surgery, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Petr KyselaDepartment of Surgery, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID http://orcid.org/0000-0003-3487-5246
Lenka OstřížkováDepartment of Hematology, Oncology and Internal Medicine, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Vladimír PaličkaInstitute of Clinical Biochemistry and Diagnostics, University Hospital Hradec Králové, Hradec Králové, Czech Republic.ORCID http://orcid.org/0000-0001-7236-1647
Alena Hyršlová VaculováDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Královopolská 135, 612 65, Brno, Czech Republic. vaculova@ibp.cz.ORCID http://orcid.org/0000-0002-0445-8807
Masaryk University · CZCzech Academy of Sciences, Institute of Biophysics · CZUniversity Hospital Hradec Králové · CZCentral European Institute of Technology · CZCzech Academy of Sciences · CZ

Funding

Akademie Věd České Republiky RVO:68081707Ministerstvo Zdravotnictví Ceské Republiky 17-28231AMinisterstvo Zdravotnictví Ceské Republiky DRO (UHHK, 00179906)
6 · The paper itself

Abstract

backgroundHepatocellular 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.

methodsWe 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.

resultsWe 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.

conclusionsOur 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.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsBiotransformationCell Line, TumorCytochrome P-450 CYP1A2Down-RegulationGene Expression Regulation, NeoplasticHepatocytesHumansMicroRNAsXenobioticsCYP1A2 protein, humanCytochrome P-450 CYP1A2MicroRNAsMIRN29C microRNA, humanMIRN653 microRNA, humanXenobioticsAHRBiotransformationCYP1A2Hepatocellular carcinomamicroRNA

Identifiers

PMID34780054
OpenAlexW3212434399

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.