Evidence map›Paper›PMID 34611144›Full record

ReviewCell death discovery2021

Ferroptosis in liver disease: new insights into disease mechanisms.

Jing Wu, Yi Wang, Rongtao Jiang, Ran Xue, Xuehong Yin, Muchen Wu, Qinghua Meng

Open access · goldAbstract readReview
In one paragraph

Review in Cell death discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 165 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed, 2 pooled it
28.0field-weighted citation impact, top 1% 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

165 citing papers in PubMed, 2 syntheses or guidelines pooled it, 265 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Ferroptosis in liver biology and diseases.Hepatology communications · 2026
    Review
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  18. PMEnvironment & health (Washington, D.C.) · 2026
    Article
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105 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 1 country.

Jing WuDepartment of Medical Oncology, Beijing You-An Hospital, Capital Medical University, Beijing, 100069, China.
Yi WangState Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, Beijing, 102206, China. yves.wangy@vip.163.com.ORCID http://orcid.org/0000-0002-4954-6317
Rongtao JiangBrainnetome Center and National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, China.
Ran XueKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, 100036, China.
Xuehong YinDepartment of Medical Oncology, Beijing You-An Hospital, Capital Medical University, Beijing, 100069, China.
Muchen WuDepartment of Medical Oncology, Beijing You-An Hospital, Capital Medical University, Beijing, 100069, China.
Qinghua MengDepartment of Medical Oncology, Beijing You-An Hospital, Capital Medical University, Beijing, 100069, China. meng_qh0805@ccmu.edu.cn.ORCID http://orcid.org/0000-0002-1989-4441
Capital Medical University · CNBeijing Proteome Research Center · CNChinese Academy of Sciences · CNPeking University · CN

Funding

Capital Health Research and Development of Special 2018-1-3011National Natural Science Foundation of China (National Science Foundation of China) 8170877
6 · The paper itself

Abstract

Characterized by excessive iron accumulation and lipid peroxidation, ferroptosis is a novel form of iron-dependent cell death, which is morphologically, genetically, and biochemically distinct from other well-known cell death. In recent years, ferroptosis has been quickly gaining attention in the field of liver diseases, as the liver is predisposed to oxidative injury and generally, excessive iron accumulation is a primary characteristic of most major liver diseases. In the current review, we first delineate three cellular defense mechanisms against ferroptosis (GPx4 in the mitochondria and cytosol, FSP1 on plasma membrane, and DHODH in mitochondria), along with four canonical modulators of ferroptosis (system Xc

Identifiers

PMID34611144
PMCPMC8492622
OpenAlexW3202493769

What OpenQuestion 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 OpenQuestion graph.