Evidence map›Paper›PMID 31641113›Full record

ArticleNature communications2019

GTPase-activating protein Rasal1 associates with ZAP-70 of the TCR and negatively regulates T-cell tumor immunity.

Youg Raj Thaker, Monika Raab, Klaus Strebhardt, Christopher E Rudd

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  3. CD4/CD8-p56Biomolecules · 2025
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  10. Tumor-infiltrating CD8Drug discovery today · 2021
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
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 3 institutions in 4 countries.

Youg Raj ThakerCell Signalling Section, Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QP, UK.
Monika RaabDepartment of Obstetrics and Gynaecology, School of Medicine, J.W. Goethe-University, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany.
Klaus StrebhardtDepartment of Obstetrics and Gynaecology, School of Medicine, J.W. Goethe-University, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany.ORCID http://orcid.org/0000-0003-2173-9763
Christopher E RuddCell Signalling Section, Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QP, UK. christopher.e.rudd@umontreal.ca.
Goethe University Frankfurt · DEHôpital Maisonneuve-Rosemont · CAUniversity of Essex · GB

Funding

Wellcome Trust 092627/Z/10/Z
6 · The paper itself

Abstract

Immunotherapy involving checkpoint blockades of inhibitory co-receptors is effective in combating cancer. Despite this, the full range of mediators that inhibit T-cell activation and influence anti-tumor immunity is unclear. Here, we identify the GTPase-activating protein (GAP) Rasal1 as a novel TCR-ZAP-70 binding protein that negatively regulates T-cell activation and tumor immunity. Rasal1 inhibits via two pathways, the binding and inhibition of the kinase domain of ZAP-70, and GAP inhibition of the p21

Indexed as

AnimalsCD4-Positive T-LymphocytesExtracellular Signal-Regulated MAP KinasesFemaleGTPase-Activating ProteinsLymphocyte ActivationMaleMelanoma, ExperimentalMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicProtein DomainsReceptors, Antigen, T-CellRNA, Small InterferingT-LymphocytesZAP-70 Protein-Tyrosine KinaseExtracellular Signal-Regulated MAP KinasesGTPase-Activating ProteinsRASAL1 protein, mouseReceptors, Antigen, T-CellRNA, Small InterferingZap70 protein, mouseZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID31641113
PMCPMC6805919
OpenAlexW2981430225

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.