Evidence map›Paper›PMID 39090079›Full record

ArticleNature communications2024

A male mouse model for metabolic dysfunction-associated steatotic liver disease and hepatocellular carcinoma.

Byung-Kwan Jeong, Won-Il Choi, Wonsuk Choi, Jieun Moon, Won Hee Lee, Chan Choi, In Young Choi, Sang-Hyun Lee, Jung Kuk Kim, Young Seok Ju and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–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

51 citing papers in PubMed.

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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

14 authors.

Byung-Kwan Jeong *Graduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Korea.ORCID 0000-0002-0038-3959
Won-Il Choi *Graduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Korea.ORCID 0000-0002-4837-0436
Wonsuk Choi *Department of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, Hwasun, Korea. wonsuc1@uci.edu.
Jieun MoonGraduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Korea.
Won Hee LeeGraduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Korea.
Chan ChoiDepartment of Pathology, Chonnam National University Medical School, Hwasun, Korea.
In Young ChoiHanmi Research Center, Hanmi Pharmaceutical Co. Ltd, Hwaseong, Korea.
Sang-Hyun LeeHanmi Research Center, Hanmi Pharmaceutical Co. Ltd, Hwaseong, Korea.
Jung Kuk KimHanmi Research Center, Hanmi Pharmaceutical Co. Ltd, Hwaseong, Korea.ORCID 0000-0001-6351-7355
Young Seok JuGraduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Korea.ORCID 0000-0002-5514-4189
Pilhan KimGraduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Korea.ORCID 0000-0001-8388-1840
Young-Ah MoonDepartment of Molecular Medicine, Inha University College of Medicine, Incheon, 22212, Korea.
Jun Yong ParkDepartment of Internal Medicine, Yonsei University College of Medicine, Yonsei Liver Center, Severance Hospital, Seoul, Korea. drpjy@yuhs.ac.ORCID 0000-0001-6324-2224
Hail KimGraduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Korea. hailkim@kaist.edu.ORCID 0000-0002-6652-1349

Funding

National Research Foundation of Korea (NRF) 2020M3A9E403869513
6 · The paper itself

Abstract

The lack of an appropriate preclinical model of metabolic dysfunction-associated steatotic liver disease (MASLD) that recapitulates the whole disease spectrum impedes exploration of disease pathophysiology and the development of effective treatment strategies. Here, we develop a mouse model (Streptozotocin with high-fat diet, STZ + HFD) that gradually develops fatty liver, metabolic dysfunction-associated steatohepatitis (MASH), hepatic fibrosis, and hepatocellular carcinoma (HCC) in the context of metabolic dysfunction. The hepatic transcriptomic features of STZ + HFD mice closely reflect those of patients with obesity accompanying type 2 diabetes mellitus, MASH, and MASLD-related HCC. Dietary changes and tirzepatide administration alleviate MASH, hepatic fibrosis, and hepatic tumorigenesis in STZ + HFD mice. In conclusion, a murine model recapitulating the main histopathologic, transcriptomic, and metabolic alterations observed in MASLD patients is successfully established.

Indexed as

Carcinoma, HepatocellularDiet, High-FatDisease Models, AnimalLiver NeoplasmsAnimalsDiabetes Mellitus, Type 2Fatty LiverHumansLiverLiver CirrhosisMaleMiceMice, Inbred C57BLNon-alcoholic Fatty Liver DiseaseObesityStreptozocinStreptozocin

Identifiers

PMID39090079
PMCPMC11294468

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.