Evidence map›Paper›PMID 38858387›Full record

ArticleCell death & disease2024

Necroptosis stimulates interferon-mediated protective anti-tumor immunity.

A Justin Rucker, Christa S Park, Qi Jing Li, E Ashley Moseman, Francis Ka-Ming Chan

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Structural and molecular principles of DAMP biology.Nature structural & molecular biology · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Regulated cell death programs shaping cancer therapy.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

A Justin RuckerDepartment of Integrative Immunobiology, Duke University School of Medicine, Durham, NC, 27710-3010, USA.
Christa S ParkDepartment of Integrative Immunobiology, Duke University School of Medicine, Durham, NC, 27710-3010, USA.ORCID 0000-0001-5003-2199
Qi Jing LiInstitute of Molecular & Cell Biology, A-STAR, Singapore, Singapore.ORCID 0000-0002-0542-9784
E Ashley MosemanDepartment of Integrative Immunobiology, Duke University School of Medicine, Durham, NC, 27710-3010, USA. ashley.moseman@duke.edu.
Francis Ka-Ming ChanDepartment of Cardiology of the Second Affiliated Hospital of Zhejiang University, State Key Laboratory of Transvascular Implantation Devices, Heart Regeneration and Repair Key Laboratory of Zhejiang Province, Hangzhou, 310009, China. fkmchan@zju.edu.cn.ORCID 0000-0002-4803-8353

Funding

TRAINING IN IMMUNOLOGY (COMPETITIVE RENEWAL OF AI07439)T32AI007349 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J. · 1989 to 2024
$4.5M
Viral inhibition of cell death in host immune responsesR01AI148302 · NIAID · DUKE UNIVERSITY · PI MIAO, EDWARD A · 2020 to 2024
$3.0M
Treatment of Primary Amoebic Meningoencephalitis via Modulation of Antibody Effector FunctionsR01NS121067 · NINDS · DUKE UNIVERSITY · PI MOSEMAN, E. ASHLEY · 2021 to 2025
$2.0M
Advanced Immunobiology Traning Program for SurgeonsT32AI141342 · NIAID · DUKE UNIVERSITY · PI Allan D. Kirk, GEORGIA Doris TOMARAS · 2019 to 2026
$1.8M
National Natural Science Foundation of China (National Science Foundation of China) 32350710189NIAID NIH HHS R01 AI148302NIAID NIH HHS T32 AI007349NIAID NIH HHS T32 AI141342NINDS NIH HHS R01 NS121067U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) 5T32AI141342U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI007349U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R01AI148302U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS121067
6 · The paper itself

Abstract

Necroptosis is an inflammatory form of cell suicide that critically depends on the kinase activity of Receptor Interacting Protein Kinase 3 (RIPK3). Previous studies showed that immunization with necroptotic cells conferred protection against subsequent tumor challenge. Since RIPK3 can also promote apoptosis and NF-κB-dependent inflammation, it remains difficult to determine the contribution of necroptosis-associated release of damage-associated molecular patterns (DAMPs) in anti-tumor immunity. Here, we describe a system that allows us to selectively induce RIPK3-dependent necroptosis or apoptosis with minimal NF-κB-dependent inflammatory cytokine expression. In a syngeneic tumor challenge model, immunization with necroptotic cells conferred superior protection against subsequent tumor challenge. Surprisingly, this protective effect required CD4

Indexed as

NecroptosisReceptor-Interacting Protein Serine-Threonine KinasesAnimalsApoptosisCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorHumansInterferon Type IMiceMice, Inbred C57BLNeoplasmsNF-kappa BSignal TransductionInterferon Type INF-kappa BReceptor-Interacting Protein Serine-Threonine KinasesRipk3 protein, mouse

Identifiers

PMID38858387
PMCPMC11164861

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.