Evidence map›Paper›PMID 24346035›Full record

ReviewNature chemical biology2014

The role of iron and reactive oxygen species in cell death.

Scott J Dixon, Brent R Stockwell

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature chemical biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,130 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,130citing papers in PubMed, 1 pooled it
47.6field-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

1,130 citing papers in PubMed, 1 synthesis or guideline pooled it, 2,307 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Multimodal microscopic and spectroscopic characterisation of heterogeneous iron oxyhydroxides in the human globus pallidus.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Cell death network regulation in HSV infection: immune evasion versus host defense.Apoptosis : an international journal on programmed cell death · 2026
    Review
  18. FePlants (Basel, Switzerland) · 2026
    Article
  19. Article
  20. Menaquinone-4 protects CD8Science China. Life sciences · 2026
    Article

1,070 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

2 authors at 1 institution in 1 country.

Scott J Dixon1] Department of Biological Sciences, Columbia University, New York, New York, USA. [2] Department of Biology, Stanford University, Stanford, California, USA.
Brent R Stockwell1] Department of Biological Sciences, Columbia University, New York, New York, USA. [2] Department of Chemistry, Columbia University, New York, New York, USA. [3] Department of Systems Biology, Columbia University, New York, New York, USA. [4] Howard Hughes Medical Institute, Columbia University, New York, New York, USA.
Columbia University · US

Funding

Chemical Genetic Profiling of Engineered Tumor CellsR01CA097061 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI STOCKWELL, BRENT R. · 2002 to 2016
$4.8M
Defining a novel trigger for apoptosisR01GM085081 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI STOCKWELL, BRENT R. · 2008 to 2011
$1.5M
Comparing HTS with Fragment-Based Design for B-Raf and the Ras-Raf InteractionR01CA161061 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI STOCKWELL, BRENT R. · 2011 to 2014
$1.0M
Targeting Tumor Cell Iron Addiction to Achieve Tumor-Selective Cell DeathR00CA166517 · NCI · STANFORD UNIVERSITY · PI DIXON, SCOTT · 2014 to 2016
$708k
Targeting Tumor Cell Iron Addiction to Achieve Tumor-Selective Cell DeathK99CA166517 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DIXON, SCOTT · 2012 to 2013
$250k
Howard Hughes Medical InstituteNCI NIH HHS 1K99CA166517-01NCI NIH HHS 5R01CA097061NCI NIH HHS R00 CA166517NCI NIH HHS R01 CA097061NCI NIH HHS R01CA161061NIGMS NIH HHS 5R01GM085081
6 · The paper itself

Abstract

The transition metal iron is essential for life, yet potentially toxic iron-catalyzed reactive oxygen species (ROS) are unavoidable in an oxygen-rich environment. Iron and ROS are increasingly recognized as important initiators and mediators of cell death in a variety of organisms and pathological situations. Here, we review recent discoveries regarding the mechanism by which iron and ROS participate in cell death. We describe the different roles of iron in triggering cell death, targets of iron-dependent ROS that mediate cell death and a new form of iron-dependent cell death termed ferroptosis. Recent advances in understanding the role of iron and ROS in cell death offer unexpected surprises and suggest new therapeutic avenues to treat cancer, organ damage and degenerative disease.

Indexed as

Cell DeathHumansIronReactive Oxygen SpeciesSignal TransductionIronReactive Oxygen Species

Identifiers

PMID24346035
OpenAlexW2011538447

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.