Evidence map›Paper›PMID 30552362›Full record

ArticleScientific reports2018

Selective overexpression of cytoglobin in stellate cells attenuates thioacetamide-induced liver fibrosis in mice.

Nguyen Thi Thanh Hai, Le Thi Thanh Thuy, Akira Shiota, Chiho Kadono, Atsuko Daikoku, Dinh Viet Hoang, Ninh Quoc Dat, Misako Sato-Matsubara, Katsutoshi Yoshizato, Norifumi Kawada

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  7. Insights into the function of cytoglobin.Biochemical Society transactions · 2023
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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 at 3 institutions in 2 countries.

Nguyen Thi Thanh HaiDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.ORCID http://orcid.org/0000-0003-2809-1859
Le Thi Thanh ThuyDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Akira ShiotaPhoenixBio Co. Ltd., Hiroshima, Japan.
Chiho KadonoDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Atsuko DaikokuDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Dinh Viet HoangDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Ninh Quoc DatDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Misako Sato-MatsubaraDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Katsutoshi YoshizatoDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Norifumi KawadaDepartments of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan. kawadanori@med.osaka-cu.ac.jp.
Osaka City University · JPHanoi Medical University · VNPhoenixBio (Japan) · JP

Funding

Japan Agency for Medical Research and Development (AMED) 18fk0210004h0003Japan Society for the Promotion of Science (JSPS) 16H05290Japan Society for the Promotion of Science (JSPS) 25293177Japan Society for the Promotion of Science (JSPS) J162640045
6 · The paper itself

Abstract

Cytoglobin (CYGB), discovered in hepatic stellate cells (HSCs), is known to possess a radical scavenger function, but its pathophysiological roles remain unclear. Here, for the first time, we generated a new transgenic (TG) mouse line in which both Cygb and mCherry reporter gene expression were under the control of the native Cygb gene promoter. We demonstrated that the expression of Cygb-mCherry was related to endogenous Cygb in adult tissues by tracing mCherry fluorescence together with DNA, mRNA, and protein analyses. Administration of a single dose (50 mg/kg) of thioacetamide (TAA) in Cygb-TG mice resulted in lower levels of alanine transaminase and oxidative stress than those in WT mice. After 10 weeks of TAA administration, Cygb-TG livers exhibited reduced neutrophil accumulation, cytokine expression and fibrosis but high levels of quiescent HSCs. Primary HSCs isolated from Cygb-TG mice (HSC

Indexed as

Gene ExpressionAnimalsArtificial Gene FusionCytoglobinGenes, ReporterHepatic Stellate CellsLiverLiver CirrhosisLuminescent ProteinsMiceMice, TransgenicPromoter Regions, GeneticRed Fluorescent ProteinThioacetamideCytoglobinLuminescent ProteinsRed Fluorescent ProteinThioacetamide

Identifiers

PMID30552362
PMCPMC6294752
OpenAlexW2904819988

What OpenQuestion 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 OpenQuestion graph.