Evidence map›Paper›PMID 41608638›Full record

ArticleInternational journal of biological sciences2026

TM4SF5-mediated KEAP1 Regulation in Hepatocytes Irrelevant to NRF2 Expression and Activity Promotes Oxidative Stress and Inflammation to Develop Metabolic Dysfunction-Associated Steatotic Liver Disease.

Eun-Ae Shin, Haesong Lee, Kyung-Hee Pyo, Wonsik Kim, Soyeon Kim, Jae-Ho Lee, Seo Hee Jin, Eunmi Kim, Soo-Min Byeon, Dong Joo Kim and 12 more

Abstract read
In one paragraph

Article in International journal of biological sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

22 authors.

Eun-Ae ShinDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Haesong LeeDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Kyung-Hee PyoDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Wonsik KimDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Soyeon KimDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Jae-Ho LeeDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Seo Hee JinDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Eunmi KimResearch Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Soo-Min ByeonDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Dong Joo KimDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Young Jun ChoDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Tae Won KimDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Minjae OhnDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Hyojung LeeDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Jeongwon LeeDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Jinwook JeongDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Doojin KimDepartment of Surgery, Gachon University Gil Medical Center, Gachon University School of Medicine, Incheon 21565, Republic of Korea.
Jie ZhengDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Han Ah LeeDepartment of Internal Medicine, Chung-Ang University College of Medicine, Seoul 06974, Republic of Korea.
Hwi Young KimDepartment of Internal Medicine, Ewha Womans University College of Medicine, Division of Gastroenterology and Hepatology, Ewha Womans University Mokdong Hospital, Seoul 07985, Republic of Korea.
Young-Joon SurhDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Jung Weon LeeDepartment of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic dysfunction-associated steatohepatitis (MASH)-associated fibrosis involves inflammation accompanied by reactive oxygen species (ROS), in addition to abnormal lipid metabolism and extracellular matrix (ECM) deposition. ROS levels are regulated by the NRF2-KEAP1 pathway. Transmembrane 4 L six family member 5 (TM4SF5) is implicated in metabolic dysfunction-associated steatotic liver disease (MASLD). However, it remains unknown how hepatocyte TM4SF5 modulates abnormal lipid and ROS accumulations during MASLD development. Here we assessed the influence of TM4SF5 on NRF2-KEAP1 pathway utilizing various

Indexed as

Fatty LiverHepatocytesInflammationKelch-Like ECH-Associated Protein 1Membrane ProteinsNF-E2-Related Factor 2AnimalsHumansMaleMiceMice, Inbred C57BLMice, KnockoutOxidative StressReactive Oxygen SpeciesKeap1 protein, mouseKelch-Like ECH-Associated Protein 1Membrane ProteinsNF-E2-Related Factor 2Reactive Oxygen SpeciesTM4SF5 protein, humanKEAP1lipid toxicitymetabolic dysfunction-associated steatohepatitisreactive oxygen speciestetraspanin

Identifiers

PMID41608638
PMCPMC12836525

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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.