Evidence map›Paper›PMID 36768453›Full record

ArticleInternational journal of molecular sciences2023

4-Methylumbelliferone Targets Revealed by Public Data Analysis and Liver Transcriptome Sequencing.

Alexandra A Tsitrina, Noreen Halimani, Irina N Andreichenko, Marat Sabirov, Mikhail Nesterchuk, Nataliya O Dashenkova, Roman Romanov, Elena V Bulgakova, Arsen Mikaelyan, Yuri Kotelevtsev

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

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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

10 authors.

Alexandra A TsitrinaKoltzov Institute of Developmental Biology, 26 Vavilov Str., 119334 Moscow, Russia.
Noreen HalimaniV. Zelman Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, 143025 Moscow, Russia.ORCID 0000-0001-6004-226X
Irina N AndreichenkoV. Zelman Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, 143025 Moscow, Russia.
Marat SabirovKoltzov Institute of Developmental Biology, 26 Vavilov Str., 119334 Moscow, Russia.
Mikhail NesterchukV. Zelman Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, 143025 Moscow, Russia.
Nataliya O DashenkovaKoltzov Institute of Developmental Biology, 26 Vavilov Str., 119334 Moscow, Russia.
Roman RomanovDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Spitalgasse 4, A-1090 Vienna, Austria.
Elena V BulgakovaKoltzov Institute of Developmental Biology, 26 Vavilov Str., 119334 Moscow, Russia.
Arsen MikaelyanKoltzov Institute of Developmental Biology, 26 Vavilov Str., 119334 Moscow, Russia.ORCID 0000-0003-4358-2357
Yuri KotelevtsevV. Zelman Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, 143025 Moscow, Russia.ORCID 0000-0002-7255-7794

Funding

IDB RAS Government basic research program 0088-2021-0017Russian Foundation for Basic Research 19-29-04123
6 · The paper itself

Abstract

4-methylumbelliferone (4MU) is a well-known hyaluronic acid synthesis inhibitor and an approved drug for the treatment of cholestasis. In animal models, 4MU decreases inflammation, reduces fibrosis, and lowers body weight, serum cholesterol, and insulin resistance. It also inhibits tumor progression and metastasis. The broad spectrum of effects suggests multiple and yet unknown targets of 4MU. Aiming at 4MU target deconvolution, we have analyzed publicly available data bases, including: 1. Small molecule library Bio Assay screening (PubChemBioAssay); 2. GO pathway databases screening; 3. Protein Atlas Database. We also performed comparative liver transcriptome analysis of mice on normal diet and mice fed with 4MU for two weeks. Potential targets of 4MU public data base analysis fall into two big groups, enzymes and transcription factors (TFs), including 13 members of the nuclear receptor superfamily regulating lipid and carbohydrate metabolism. Transcriptome analysis revealed changes in the expression of genes involved in bile acid metabolism, gluconeogenesis, and immune response. It was found that 4MU feeding decreased the accumulation of the glycogen granules in the liver. Thus, 4MU has multiple targets and can regulate cell metabolism by modulating signaling via nuclear receptors.

Indexed as

HymecromoneTranscriptomeAnimalsInflammationLipid MetabolismLiverMiceSignal TransductionHymecromone4-methylumbelliferonecarbohydrate metabolismlipid metabolismnuclear receptorsRNA-Seq

Identifiers

PMID36768453
PMCPMC9917189

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.