Evidence map›Paper›PMID 40965654›Full record

ReviewJournal of gastroenterology2025

Ferroptosis: biology and role in liver disease.

Keisuke Hino, Sohji Nishina, Izumi Yanatori

Abstract readReview
In one paragraph

Review in Journal of gastroenterology, 2025. 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
–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

12 citing papers in PubMed.

  1. Article
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  5. Article
  6. Review
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  10. Article
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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

3 authors.

Keisuke HinoDigestive Disease Center, Shunan Memorial Hospital, 1-10-1 Ikunoya-Minami, Kudamatsu, Yamaguchi, 744-0033, Japan. khino@med.kawasaki-m.ac.jp.ORCID 0000-0002-3297-1720
Sohji NishinaDepartment of Gastroenterology and Hepatology, Kawasaki Medical School, Kurashiki, Japan.
Izumi YanatoriDepartment of Molecular and Cellular Physiology, Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan. yanatori@mcp.med.kyoto-u.ac.jp.

Funding

Fusion Oriented REsearch for disruptive Science and Technology JPMJFR226KJapan Society for the Promotion of Science JP23K06377
6 · The paper itself

Abstract

Ferroptosis is a form of nonapoptotic cell death that is driven by iron-dependent lipid peroxidation and is relevant to a wide range of biological processes, such as development, aging, immunity, and cancer. Ferroptosis has also been linked to numerous hepatic metabolic pathways, including the metabolism of iron, fatty acids, and amino acids, such as cysteine. During the last decade, studies on the biology of and molecules regulating ferroptosis have shed light on the role of ferroptosis in liver disease and its implications. The susceptibility of liver cells to ferroptosis determines the extent of liver injury and affects the progression of nonneoplastic diseases, whereas liver cancer cells display intrinsic or acquired resistance to ferroptosis, which promotes cancer progression. These findings indicate that ferroptosis represents a promising target for the prevention and treatment of many forms of liver disease. In this review, we provide an update on the mechanisms regulating ferroptosis, focusing on the peroxidation of phospholipids, the antioxidant pathways that limit lipid peroxidation, and the regulation of the labile iron pool, all of which are closely connected. We also summarize the roles and importance of ferroptosis in the pathogenesis of liver disease, and the therapeutic potential of targeting ferroptosis in liver diseases.

Indexed as

FerroptosisLiver DiseasesAnimalsAntioxidantsHumansIronLipid PeroxidationPhospholipidsAntioxidantsIronPhospholipidsGlutathione peroxidase 4IronLipid peroxidationPolyunsaturated free fatty acidReactive oxygen species

Identifiers

PMID40965654
PMCPMC12549746

What Socratic holds

Textmetadata
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 Socratic graph.