Evidence map›Paper›PMID 38548850›Full record

ArticleCell death and differentiation2024

ZBP1 and TRIF trigger lethal necroptosis in mice lacking caspase-8 and TNFR1.

Margaret Solon, Nianfeng Ge, Shannon Hambro, Susan Haller, Jian Jiang, Miriam Baca, Jessica Preston, Allie Maltzman, Katherine E Wickliffe, Yuxin Liang and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Mechanisms, regulation and clinical relevance of necroptosis.Nature reviews. Molecular cell biology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Role of PANoptosis in cancer: Molecular mechanisms and therapeutic opportunities.Apoptosis : an international journal on programmed cell death · 2025
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  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

14 authors at 1 institution in 1 country.

Margaret SolonDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Nianfeng GeDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Shannon HambroDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Susan HallerDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Jian JiangDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Miriam BacaDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Jessica PrestonDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Allie MaltzmanDepartment of Physiological Chemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Katherine E WickliffeDepartment of Physiological Chemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Yuxin LiangDepartment of Microchemistry, Proteomics, Lipidomics, and Next Generation Sequencing, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Rohit RejaDepartment of Physiological Chemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Dorothee NicklesDepartment of Oncology Bioinformatics, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Kim NewtonDepartment of Physiological Chemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA. knewton@gene.com.
Joshua D WebsterDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA. websterj@gene.com.ORCID 0000-0002-0014-1685
Gene Therapy Laboratory · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Necroptosis is a lytic form of cell death that is mediated by the kinase RIPK3 and the pseudokinase MLKL when caspase-8 is inhibited downstream of death receptors, toll-like receptor 3 (TLR3), TLR4, and the intracellular Z-form nucleic acid sensor ZBP1. Oligomerization and activation of RIPK3 is driven by interactions with the kinase RIPK1, the TLR adaptor TRIF, or ZBP1. In this study, we use immunohistochemistry (IHC) and in situ hybridization (ISH) assays to generate a tissue atlas characterizing RIPK1, RIPK3, Mlkl, and ZBP1 expression in mouse tissues. RIPK1, RIPK3, and Mlkl were co-expressed in most immune cell populations, endothelial cells, and many barrier epithelia. ZBP1 was expressed in many immune populations, but had more variable expression in epithelia compared to RIPK1, RIPK3, and Mlkl. Intriguingly, expression of ZBP1 was elevated in Casp8

Indexed as

Adaptor Proteins, Vesicular TransportCaspase 8Mice, KnockoutNecroptosisReceptor-Interacting Protein Serine-Threonine KinasesReceptors, Tumor Necrosis Factor, Type IRNA-Binding ProteinsAnimalsMiceMice, Inbred C57BLProtein KinasesAdaptor Proteins, Vesicular TransportCaspase 8Protein KinasesReceptor-Interacting Protein Serine-Threonine KinasesReceptors, Tumor Necrosis Factor, Type IRNA-Binding ProteinsTicam1 protein, mouseZbp1 protein, mouse

Identifiers

PMID38548850
PMCPMC11093969
OpenAlexW4393253836

What OpenQuestion holds

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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.