Evidence map›Paper›PMID 31101885›Full record

ArticleCell death and differentiation2020

RIP1 inhibition blocks inflammatory diseases but not tumor growth or metastases.

Snahel Patel, Joshua D Webster, Eugene Varfolomeev, Youngsu C Kwon, Jason H Cheng, Juan Zhang, Debra L Dugger, Kate E Wickliffe, Allie Maltzman, Swathi Sujatha-Bhaskar and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 1 pooled it
6.3field-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

86 citing papers in PubMed, 1 synthesis or guideline pooled it, 141 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Regulated cell death programs shaping cancer therapy.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
  8. RIPK1 ubiquitination regulates its kinase-independent function in development and inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Cellular Context Influences Kinase Inhibitor Selectivity.Journal of medicinal chemistry · 2026
    Article
  10. Programmed cell death of keratinocytes: an active driver in psoriasis.Apoptosis : an international journal on programmed cell death · 2026
    Review
  11. Monogenic disorders of the TNF signalling pathway.Nature reviews. Rheumatology · 2026
    Review
  12. Targeting PANoptosis: a promising therapeutic strategy for ALI/ARDS.Apoptosis : an international journal on programmed cell death · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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  20. Review

26 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

25 authors at 4 institutions in 2 countries.

Snahel PatelDepartment of Discovery Chemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA. patel.snahel@gene.com.ORCID http://orcid.org/0000-0003-2210-8963
Joshua D WebsterDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Eugene VarfolomeevDepartment of Early Discovery Biochemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Youngsu C KwonDepartment of Translational Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Jason H ChengDepartment of Molecular Oncology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Juan ZhangDepartment of Translational Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Debra L DuggerDepartment of Physiological Chemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Kate E WickliffeDepartment of Physiological Chemistry, 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.
Swathi Sujatha-BhaskarDepartments of Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Pawan Bir KohliDepartment of Biochemical and Cellular Pharmacology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Sreema RamaswamyDepartment of Biochemical and Cellular Pharmacology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Gauri DeshmukhDepartment of Drug Metabolism and Pharmacokinetics, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Bianca M LiedererDepartment of Drug Metabolism and Pharmacokinetics, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Rina FongDepartment of Structural Biology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Greg HamiltonDepartment of Discovery Chemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Patrick LupardusDepartment of Structural Biology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Patrick CaplaziDepartment of Pathology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Wyne P LeeDepartment of Translational Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Menno van Lookeren CampagneDepartments of Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Adam JohnsonDepartment of Biochemical and Cellular Pharmacology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.ORCID http://orcid.org/0000-0003-1459-4236
Brent S McKenzieDepartment of Translational Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Melissa R JunttilaDepartment of Molecular Oncology, 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.
Domagoj VucicDepartment of Early Discovery Biochemistry, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA. domagoj@gene.com.
Gene Therapy Laboratory · FRMolecular Oncology (United States) · USAmgen (United States) · USGilead Sciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The kinase RIP1 acts in multiple signaling pathways to regulate inflammatory responses and it can trigger both apoptosis and necroptosis. Its kinase activity has been implicated in a range of inflammatory, neurodegenerative, and oncogenic diseases. Here, we explore the effect of inhibiting RIP1 genetically, using knock-in mice that express catalytically inactive RIP1 D138N, or pharmacologically, using the murine-potent inhibitor GNE684. Inhibition of RIP1 reduced collagen antibody-induced arthritis, and prevented skin inflammation caused by mutation of Sharpin, or colitis caused by deletion of Nemo from intestinal epithelial cells. Conversely, inhibition of RIP1 had no effect on tumor growth or survival in pancreatic tumor models driven by mutant Kras, nor did it reduce lung metastases in a B16 melanoma model. Collectively, our data emphasize a role for the kinase activity of RIP1 in certain inflammatory disease models, but question its relevance to tumor progression and metastases.

Indexed as

AnimalsArthritisCell DeathCell LineCell Line, TumorColitisDermatitisFemaleGene Knock-In TechniquesHumansIleitisInflammationIntracellular Signaling Peptides and ProteinsMaleMelanoma, ExperimentalMiceIntracellular Signaling Peptides and ProteinsNEMO protein, mouseProtein Kinase InhibitorsProtein Serine-Threonine KinasesReceptor-Interacting Protein Serine-Threonine KinasesRIPK1 protein, humanRipk1 protein, mouseRIPK1 protein, ratRipk3 protein, mouse

Identifiers

PMID31101885
PMCPMC7206119
OpenAlexW2945990504

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.