Evidence map›Paper›PMID 27514700›Full record

ArticleCell research2016

Ferroptosis is an autophagic cell death process.

Minghui Gao, Prashant Monian, Qiuhui Pan, Wei Zhang, Jenny Xiang, Xuejun Jiang

Open access · bronzeAbstract read
In one paragraph

Article in Cell research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,080 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,080citing papers in PubMed, 3 pooled it
43.0field-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

1,080 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,777 citations in OpenAlex.

  1. Pooled it
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  3. Pooled it
  4. Article
  5. PROTACs in cancer therapy: targeted degradation of GPX4, PARP and epigenetic regulators.Journal of enzyme inhibition and medicinal chemistry · 2026
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  10. Ferroptosis in liver biology and diseases.Hepatology communications · 2026
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1,020 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

6 authors at 3 institutions in 2 countries.

Minghui GaoDepartment of Clinical Laboratory, Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Prashant MonianCell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.
Qiuhui PanCell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.
Wei ZhangGenomics Resources Core Facility, Weill Cornell Medical College, New York, USA.
Jenny XiangGenomics Resources Core Facility, Weill Cornell Medical College, New York, USA.
Xuejun JiangCell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.
Memorial Sloan Kettering Cancer Center · USCornell University · USShanghai Children's Medical Center · CN

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Mechanisms and Function of Autophagy in CancerR01CA166413 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JIANG, XUEJUN · 2013 to 2023
$3.9M
Role of the ULK1 Complex in AutophagyR01GM113013 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI JIANG, XUEJUN · 2015 to 2018
$1.5M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA166413NIGMS NIH HHS R01 GM113013
6 · The paper itself

Abstract

Ferroptosis is an iron-dependent form of regulated necrosis. It is implicated in various human diseases, including ischemic organ damage and cancer. Here, we report the crucial role of autophagy, particularly autophagic degradation of cellular iron storage proteins (a process known as ferritinophagy), in ferroptosis. Using RNAi screening coupled with subsequent genetic analysis, we identified multiple autophagy-related genes as positive regulators of ferroptosis. Ferroptosis induction led to autophagy activation and consequent degradation of ferritin and ferritinophagy cargo receptor NCOA4. Consistently, inhibition of ferritinophagy by blockage of autophagy or knockdown of NCOA4 abrogated the accumulation of ferroptosis-associated cellular labile iron and reactive oxygen species, as well as eventual ferroptotic cell death. Therefore, ferroptosis is an autophagic cell death process, and NCOA4-mediated ferritinophagy supports ferroptosis by controlling cellular iron homeostasis.

Indexed as

AnimalsApoptosisAutophagyFerritinsGenetic TestingHomeostasisHumansIronMiceNuclear Receptor CoactivatorsReactive Oxygen SpeciesRNA InterferenceFerritinsIronNCOA4 protein, humanNcoA4 protein, mouseNuclear Receptor CoactivatorsReactive Oxygen Species

Identifiers

PMID27514700
PMCPMC5034113
OpenAlexW2518357275

What OpenQuestion holds

Textmetadata
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.