Evidence map›Paper›PMID 26485505›Full record

ArticleThe American journal of pathology2015

Mice with Hepatic Loss of the Desmosomal Protein γ-Catenin Are Prone to Cholestatic Injury and Chemical Carcinogenesis.

Lili Zhou, Tirthadipa Pradhan-Sundd, Minakshi Poddar, Sucha Singh, Alex Kikuchi, Donna B Stolz, Weinian Shou, Zongfang Li, Kari N Nejak-Bowen, Satdarshan P Monga

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2015. 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
0.6field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Wnt/β-Catenin Signaling in Liver Pathobiology.Annual review of pathology · 2025
    Review
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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.

Lili ZhouDepartment of General Surgery, The Second Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, China; Department of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Tirthadipa Pradhan-SunddDepartment of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Minakshi PoddarDepartment of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Sucha SinghDepartment of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Alex KikuchiDepartment of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Donna B StolzDepartment of Cell Biology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Weinian ShouDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana.
Zongfang LiDepartment of General Surgery, The Second Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, China.
Kari N Nejak-BowenDepartment of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Satdarshan P MongaDepartment of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania; Department of Medicine, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania. Electronic address: smonga@pitt.edu.
University of Pittsburgh · USIndiana University School of MedicineSecond Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

Role of Wnt/Beta-Catenin Signaling in Liver DevelopmentR01DK062277 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Satdarshan Singh Monga · 2004 to 2026
$9.0M
Digestive Diseases Training ProgramT32DK063922 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ARTEEL, GAVIN E, YADAV, DHIRAJ · 2003 to 2022
$5.2M
Targeting beta-catenin in liver pathology: Novel Interactions, Novel ParadigmsR01DK100287 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MONGA, SATDARSHAN SINGH · 2013 to 2016
$1.3M
NIDDK NIH HHS 1R01DK100287NIDDK NIH HHS 1R01DK62277NIDDK NIH HHS 5T32DK63922-13NIDDK NIH HHS R01 DK062277NIDDK NIH HHS R01 DK100287NIDDK NIH HHS T32 DK063922
6 · The paper itself

Abstract

γ-Catenin, an important component of desmosomes, may also participate in Wnt signaling. Herein, we dissect the role of γ-catenin in liver by generating conditional γ-catenin knockout (KO) mice and assessing their phenotype after bile duct ligation (BDL) and diethylnitrosamine-induced chemical carcinogenesis. At baseline, KO and wild-type littermates showed comparable serum biochemistry, liver histology, and global gene expression. β-Catenin protein was modestly increased without any change in Wnt signaling. Desmosomes were maintained in KO, and despite no noticeable changes in gene expression, differential detergent fractionation revealed quantitative and qualitative changes in desmosomal cadherins, plaque proteins, and β-catenin. Enhanced association of β-catenin to desmoglein-2 and plakophilin-3 was observed in KO. When subjected to BDL, wild-type littermates showed specific changes in desmosomal protein expression. In KO, BDL deteriorated baseline compensatory changes, which manifested as enhanced injury and fibrosis. KO also showed enhanced tumorigenesis to diethylnitrosamine treatment because of Wnt activation, as also verified in vitro. γ-Catenin overexpression in hepatoma cells increased its binding to T-cell factor 4 at the expense of β-catenin-T-cell factor 4 association, induced unique target genes, affected Wnt targets, and reduced cell proliferation and viability. Thus, γ-catenin loss in liver is basally well tolerated. However, after insults like BDL, these compensations at desmosomes fail, and KO show enhanced injury. Also, γ-catenin negatively regulates tumor growth by affecting Wnt signaling.

Indexed as

Animalsbeta CateninBile DuctsCell Transformation, NeoplasticCholestasisDesmosomesDiethylnitrosamineFemalegamma CateninGene Expression RegulationGene Expression Regulation, NeoplasticLiverLiver Neoplasms, ExperimentalMaleMice, KnockoutNeoplasm Proteinsbeta CateninCTNNB1 protein, mouseDiethylnitrosaminegamma CateninJup protein, mouseNeoplasm Proteins

Identifiers

PMID26485505
PMCPMC4729235
OpenAlexW1751900976

What OpenQuestion holds

Textmetadata
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.