Evidence map›Paper›PMID 30283086›Full record

ArticleCell death & disease2018

CCAAT/enhancer-binding protein-β functions as a negative regulator of Wnt/β-catenin signaling through activation of AXIN1 gene expression.

Seoyoung Park, Mi-Sun Lee, Jungsug Gwak, Tae-Ik Choi, Youngseok Lee, Bong Gun Ju, Cheol-Hee Kim, Sangtaek Oh

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  7. Root Bark ofJournal of microbiology and biotechnology · 2021
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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

8 authors at 3 institutions in 1 country.

Seoyoung ParkBK21 PLUS Program, Department of Bio and Fermentation Convergence Technology, Kookmin University, Seoul, 02707, Republic of Korea.
Mi-Sun LeeDepartment of Biology, Chungnam National University, Daejeon, 34134, Republic of Korea.
Jungsug GwakDepartment of Life Science, Sogang University, Seoul, 04107, Republic of Korea.
Tae-Ik ChoiDepartment of Biology, Chungnam National University, Daejeon, 34134, Republic of Korea.
Youngseok LeeBK21 PLUS Program, Department of Bio and Fermentation Convergence Technology, Kookmin University, Seoul, 02707, Republic of Korea.
Bong Gun JuDepartment of Life Science, Sogang University, Seoul, 04107, Republic of Korea.
Cheol-Hee KimDepartment of Biology, Chungnam National University, Daejeon, 34134, Republic of Korea.ORCID http://orcid.org/0000-0002-3019-0699
Sangtaek OhBK21 PLUS Program, Department of Bio and Fermentation Convergence Technology, Kookmin University, Seoul, 02707, Republic of Korea. ohsa@kookmin.ac.kr.
Chungnam National University · KRKookmin University · KRSogang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Axin1, a concentration-limiting component of the β-catenin destruction complex, negatively regulates the Wnt/β-catenin pathway. Axin1 concentration is reported to be regulated by proteasomal degradation; however, its transcriptional regulation has not yet been reported. Here, we demonstrated that CCAAT/enhancer-binding protein-β (C/EBP-β) activates axis inhibition protein 1 (AXIN1) gene expression, thereby attenuating Wnt/β-catenin signaling. C/EBP-β interacted with cis-regulatory element for C/EBP-β in the 5'-upstream sequences of the AXIN1 gene and increased AXIN1 promoter activity. Functional analysis using Drosophila and zebrafish models established that C/EBP-β negatively regulates the Wnt/β-catenin pathway. Small-molecule-based up-regulation of C/EBP-β induces AXIN1 gene expression and down-regulates the intracellular β-catenin level, thereby inhibiting hepatoma cell growth. Thus, our findings provide a unique mechanistic insight into the regulation of Axin homeostasis and present a novel strategy for the development of anticancer therapeutics targeting Wnt/β-catenin signaling.

Indexed as

3T3-L1 CellsAnimalsAxin Proteinbeta CateninCarcinoma, HepatocellularCCAAT-Enhancer-Binding Protein-betaCell LineCell ProliferationDown-RegulationDrosophilaGene ExpressionHEK293 CellsHumansLiver NeoplasmsMiceSignal TransductionAxin Proteinbeta CateninCCAAT-Enhancer-Binding Protein-beta

Identifiers

PMID30283086
PMCPMC6170413
OpenAlexW2894589681

What OpenQuestion holds

Textmetadata
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.