Evidence map›Paper›PMID 25965523›Full record

ArticleACS chemical biology2015

Human Haploid Cell Genetics Reveals Roles for Lipid Metabolism Genes in Nonapoptotic Cell Death.

Scott J Dixon, Georg E Winter, Leila S Musavi, Eric D Lee, Berend Snijder, Manuele Rebsamen, Giulio Superti-Furga, Brent R Stockwell

Open access · greenAbstract read
In one paragraph

Article in ACS chemical biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 660 papers.

0numbers the graph read from it
0cells of the map it votes in
660citing papers in PubMed
16.0field-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

660 citing papers in PubMed, 1,002 citations in OpenAlex.

  1. Review
  2. Review
  3. Gestational Changes in Placental Iron Homeostasis are Associated With Ferroptosis-Associated Redox Signaling and Trophoblast Behavior.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  4. Ferroptosis in liver biology and diseases.Hepatology communications · 2026
    Review
  5. Ferroptosis in cancer: molecular mechanisms, biological roles, and therapeutic significance.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  6. Ferroptosis in kidney disease.Nature reviews. Nephrology · 2026
    Review
  7. Ferroptosis as a target mechanism in heart and kidney disease.The Journal of clinical investigation · 2026
    Review
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600 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

8 authors at 3 institutions in 2 countries.

Scott J Dixon⊥Department of Biology, Stanford University, 337 Campus Drive, Stanford, California 94305, United States.
Georg E Winter∥CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, 1090 Vienna, Austria.
Leila S Musavi
Eric D Lee
Berend Snijder∥CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, 1090 Vienna, Austria.
Manuele Rebsamen∥CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, 1090 Vienna, Austria.
Giulio Superti-Furga∥CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, 1090 Vienna, Austria.
Brent R Stockwell
Austrian Academy of Sciences · ATCeMM Research Center for Molecular Medicine · ATStanford 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
Howard Hughes Medical InstituteNCI NIH HHS 4R00CA166517-03NCI NIH HHS 5R01CA097061NCI NIH HHS R00 CA166517NCI NIH HHS R01 CA097061NCI NIH HHS R01 CA161061NCI NIH HHS R01CA161061NIGMS NIH HHS 5R01GM085081NIGMS NIH HHS R01 GM085081
6 · The paper itself

Abstract

Little is known about the regulation of nonapoptotic cell death. Using massive insertional mutagenesis of haploid KBM7 cells we identified nine genes involved in small-molecule-induced nonapoptotic cell death, including mediators of fatty acid metabolism (ACSL4) and lipid remodeling (LPCAT3) in ferroptosis. One novel compound, CIL56, triggered cell death dependent upon the rate-limiting de novo lipid synthetic enzyme ACC1. These results provide insight into the genetic regulation of cell death and highlight the central role of lipid metabolism in nonapoptotic cell death.

Indexed as

ApoptosisHaploidyLipid MetabolismCell Line, TumorGene Expression RegulationHumansMutagenesis, InsertionalSmall Molecule LibrariesSmall Molecule Libraries

Identifiers

PMID25965523
PMCPMC4509420
OpenAlexW323406638

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.