Evidence map›Paper›PMID 34051057›Full record

ArticleFEBS open bio2021

Activation of the mitogen-activated protein kinase ERK1/2 signaling pathway suppresses the expression of ChREBPα and β in HepG2 cells.

Lan Li, Haruhiko Sakiyama, Hironobu Eguchi, Daisaku Yoshihara, Noriko Fujiwara, Keiichiro Suzuki

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2021. 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
–field-weighted citation impact, top 90% 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, 0 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

6 authors at 1 institution in 1 country.

Lan LiDepartment of Biochemistry, Hyogo College of Medicine, Nishinomiya, Japan.
Haruhiko SakiyamaDepartment of Biochemistry, Hyogo College of Medicine, Nishinomiya, Japan.ORCID 0000-0003-0178-8744
Hironobu EguchiDepartment of Biochemistry, Hyogo College of Medicine, Nishinomiya, Japan.
Daisaku YoshiharaDepartment of Biochemistry, Hyogo College of Medicine, Nishinomiya, Japan.
Noriko FujiwaraDepartment of Biochemistry, Hyogo College of Medicine, Nishinomiya, Japan.
Keiichiro SuzukiDepartment of Biochemistry, Hyogo College of Medicine, Nishinomiya, Japan.
Hyogo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The carbohydrate response element-binding protein (ChREBP), a glucose-responsive transcription factor that plays a critical role in the glucose-mediated induction of genes involved in hepatic glycolysis and lipogenesis, exists as two isoforms: ChREBPα and ChREBPβ. However, the mechanism responsible for regulating the expression of both ChREBPα and β, as well as the mechanism that determines which specific isoform is more responsive to different stimuli, remains unclear. To address this issue, we compared the effects of several stimuli, including oxidative stress, on the mRNA and protein expression levels of ChREBPα and β in the hepatocyte cell line, HepG2. We found that H

Indexed as

MAP Kinase Signaling SystemMitogen-Activated Protein KinasesBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsHep G2 CellsHumansSignal TransductionBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsMitogen-Activated Protein KinasesChREBPαChREBPβERKoxidative stressstaurosporine

Identifiers

PMID34051057
PMCPMC8255832
OpenAlexW3165039434

What OpenQuestion holds

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LicenceCC BY
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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.