Evidence map›Paper›PMID 38152126›Full record

ArticleFrontiers in endocrinology2023

Wnt/β-catenin signaling activation promotes lipogenesis in the steatotic liver via physical mTOR interaction.

Kewei Wang, Rong Zhang, Nadja Lehwald, Guo-Zhong Tao, Bowen Liu, Bo Liu, Yangseok Koh, Karl G Sylvester

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

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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 4 institutions in 4 countries.

Kewei WangDepartment of Surgery, Divison of Pediatric Surgery, Stanford University School of Medicine, Stanford, CA, United States.
Rong ZhangDepartment of Surgery, Divison of Pediatric Surgery, Stanford University School of Medicine, Stanford, CA, United States.
Nadja LehwaldDepartment of Surgery, Divison of Pediatric Surgery, Stanford University School of Medicine, Stanford, CA, United States.
Guo-Zhong TaoDepartment of Surgery, Divison of Pediatric Surgery, Stanford University School of Medicine, Stanford, CA, United States.
Bowen LiuDepartment of Surgery, Divison of Pediatric Surgery, Stanford University School of Medicine, Stanford, CA, United States.
Bo LiuDepartment of Surgery, Divison of Pediatric Surgery, Stanford University School of Medicine, Stanford, CA, United States.
Yangseok KohDepartment of Surgery, Chonnam National University Medical School, Gwangju, Republic of Korea.
Karl G SylvesterDepartment of Surgery, Divison of Pediatric Surgery, Stanford University School of Medicine, Stanford, CA, United States.
Stanford University · USChina Medical University · CNChonnam National University · KRHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Wnt/β-catenin signaling plays an important role in regulating hepatic metabolism. This study is to explore the molecular mechanisms underlying the potential crosstalk between Wnt/β-catenin and mTOR signaling in hepatic steatosis. Methods: Transgenic mice (overexpress Wnt1 in hepatocytes, Wnt+) mice and wild-type littermates were given high fat diet (HFD) for 12 weeks to induce hepatic steatosis. Mouse hepatocytes cells (AML12) and those transfected to cause constitutive β-catenin stabilization (S33Y) were treated with oleic acid for lipid accumulation. Results: Wnt+ mice developed more hepatic steatosis in response to HFD. Immunoblot shows a significant increase in the expression of fatty acid synthesis-related genes (SREBP-1 and its downstream targets ACC, AceCS1, and FASN) and a decrease in fatty acid oxidation gene (MCAD) in Wnt+ mice livers under HFD. Wnt+ mice also revealed increased Akt signaling and its downstream target gene mTOR in response to HFD. Conclusions: Taken together, our results demonstrate that β-catenin stabilization through Wnt signaling serves a central role in lipid metabolism in the steatotic liver through up-regulation of fatty acid synthesis via Akt/mTOR signaling. These findings suggest hepatic Wnt signaling may represent a therapeutic strategy in hepatic steatosis.

Indexed as

Fatty LiverLipogenesisAnimalsbeta CateninMiceMice, TransgenicOleic AcidProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesWnt Signaling Pathwaybeta CateninOleic AcidProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinasesbeta-catenin (B-catenin)fatty acid synthesishepatic steatosishigh fat dietWnt signaling

Identifiers

PMID38152126
PMCPMC10751342
OpenAlexW4389677913

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.