Evidence map›Paper›PMID 29572095›Full record

ArticleJournal of hepatology2018

A simple diet- and chemical-induced murine NASH model with rapid progression of steatohepatitis, fibrosis and liver cancer.

Takuma Tsuchida, Youngmin A Lee, Naoto Fujiwara, Maria Ybanez, Brittany Allen, Sebastiao Martins, M Isabel Fiel, Nicolas Goossens, Hsin-I Chou, Yujin Hoshida and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Journal of hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 340 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
340citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

340 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  9. Advances in Lipid Metabolism Reprogramming in Hepatocellular Carcinoma.Journal of clinical and translational hepatology · 2026
    Review
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280 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Takuma TsuchidaDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA; Research Division, Mitsubishi Tanabe Pharma Corporation, Saitama, Japan.
Youngmin A LeeDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Naoto FujiwaraDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Maria YbanezDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Brittany AllenDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Sebastiao MartinsDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA; Departamento de Patologia, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, Brazil.
M Isabel FielDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, USA.
Nicolas GoossensDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Hsin-I ChouDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Yujin HoshidaDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Scott L FriedmanDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA. Electronic address: Scott.Friedman@mssm.edu.

Funding

Developing, Demonstrating, and Disseminating Innovative Programs to Achieve Translational SuccessUL1TR001866 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY, KRUEGER, JAMES G · 2016 to 2025
$40.6M
THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Deanna L Benson · 2015 to 2026
$35.4M
The Role of KLF6 in Hepatic FibrosisR01DK056621 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI FRIEDMAN, SCOTT L. · 2000 to 2019
$6.2M
Molecular Prognostic Indicators in Liver Cirrhosis and CancerR01DK099558 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HOSHIDA, YUJIN · 2013 to 2016
$2.6M
Autophagy during hepatic stellate cell activation in alcoholic liver injuryR01AA020709 · NIAAA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIEDMAN, SCOTT L. · 2011 to 2015
$1.8M
Hepatic autophagy, progenitor cells and fibrosisR56DK056621 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIEDMAN, SCOTT L. · 2015 to 2015
$297k
European Research Council 671231NCATS NIH HHS UL1 TR001866NCI NIH HHS P30 CA196521NIAAA NIH HHS R01 AA020709NIDDK NIH HHS R01 DK056621NIDDK NIH HHS R01 DK099558NIDDK NIH HHS R56 DK056621
6 · The paper itself

Abstract

BACKGROUND AND

aimsAlthough the majority of patients with non-alcoholic fatty liver disease (NAFLD) have only steatosis without progression, a sizeable fraction develop non-alcoholic steatohepatitis (NASH), which can lead to cirrhosis and hepatocellular carcinoma (HCC). Many established diet-induced mouse models for NASH require 24-52 weeks, which makes testing for drug response costly and time consuming.

methodsWe have sought to establish a murine NASH model with rapid progression of extensive fibrosis and HCC by using a western diet (WD), which is high-fat, high-fructose and high-cholesterol, combined with low weekly dose of intraperitoneal carbon tetrachloride (CCl

resultsC57BL/6J mice were fed a normal chow diet ± CCl

conclusionsOur mouse NASH model exhibits rapid progression of advanced fibrosis and HCC, and mimics histological, immunological and transcriptomic features of human NASH, suggesting that it will be a useful experimental tool for preclinical drug testing. LAY SUMMARY: A carefully characterized model has been developed in mice that recapitulates the progressive stages of human fatty liver disease, from simple steatosis, to inflammation, fibrosis and cancer. The functional pathways of gene expression and immune abnormalities in this model closely resemble human disease. The ease and reproducibility of this model make it ideal to study disease pathogenesis and test new treatments.

Indexed as

Diet, WesternFatty LiverLiver CirrhosisLiver NeoplasmsMice, Inbred C57BLAnimalsCarbon TetrachlorideDisease Models, AnimalDisease ProgressionGene Expression ProfilingInflammationMiceReproducibility of ResultsCarbon TetrachlorideFatty liver disease modelsFibrosisHepatic stellate cellsHepatocellular carcinomaInsulin resistanceNAFLDNASHSteatohepatitis

Identifiers

PMID29572095
PMCPMC6054570

What OpenQuestion holds

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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.