Evidence map›Paper›PMID 28854080›Full record

ArticleCell cycle (Georgetown, Tex.)2017

Biological events and molecular signaling following MLKL activation during necroptosis.

Yi-Nan Gong, Cliff Guy, Jeremy Chase Crawford, Douglas R Green

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

59 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. ALDH2 Mediated Ferroptosis Regulation in Ischemia-Reperfusion Injury.Journal of cellular and molecular medicine · 2026
    Review
  8. Article
  9. Mixed Lineage Kinase Domain-Like Protein (MLKL): From Mechanisms to Therapeutic Opportunities.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  10. Review
  11. The complexities of cell death mechanisms: a new perspective in systemic sclerosis therapy.Apoptosis : an international journal on programmed cell death · 2025
    Review
  12. Review
  13. Article
  14. Review
  15. FSP1-mediated ferroptosis in cancer: from mechanisms to therapeutic applications.Apoptosis : an international journal on programmed cell death · 2024
    Review
  16. CaProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Review
  18. Review
  19. Review
  20. Article
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

4 authors at 1 institution in 1 country.

Yi-Nan Gonga Department of Immunology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Cliff Guya Department of Immunology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Jeremy Chase Crawforda Department of Immunology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Douglas R Greena Department of Immunology , St. Jude Children's Research Hospital , Memphis , TN , USA.
St. Jude Children's Research Hospital · US

Funding

Survival Function of the Fadd-Caspase-8-Flip ComplexR01AI044828 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GREEN, DOUGLAS R. · 1999 to 2016
$6.3M
Survival Function of the Fadd-Caspase-8-Flip Complex - MERIT ExtensionR37AI044828 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Douglas R. Green · 2017 to 2026
$4.5M
To the edge of necroptosis and backR01CA169291 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GREEN, DOUGLAS R. · 2012 to 2018
$2.6M
NCI NIH HHS R01 CA169291NIAID NIH HHS R01 AI044828NIAID NIH HHS R37 AI044828
6 · The paper itself

Abstract

Necroptosis is a form of programmed necrotic cell death mediated by the kinase RIPK3 and its substrate MLKL. MLKL, which displays plasma membrane (PM) pore-forming activity upon phosphorylation, functions as the executioner during necroptosis. Thus, it was previously assumed that MLKL phosphorylation is the endpoint of the necroptotic signaling pathway. Here, we summarize several events that characterize the dying necroptotic cells after MLKL phosphorylation, including Ca

Indexed as

AnimalsApoptosisCalciumCell HypoxiaCell MembraneCobaltEndosomal Sorting Complexes Required for TransportFibroblastsGene Expression RegulationHT29 CellsHumansMacrophagesMiceModels, BiologicalNecrosisNIH 3T3 CellsCalciumCobaltcobaltous chlorideEndosomal Sorting Complexes Required for TransportMLKL protein, mousePhosphatidylserinesProtein KinasesReceptor-Interacting Protein Serine-Threonine KinasesRipk3 protein, mousecell deathESCRTMLKLNecroptosisplasma membrane repairRIPK3

Identifiers

PMID28854080
PMCPMC5628637
OpenAlexW2752261827

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.