Evidence map›Paper›PMID 28924177›Full record

ArticleScientific reports2017

Loss of MAPK-activated protein kinase 2 enables potent dendritic cell-driven anti-tumour T cell response.

Klara Soukup, Angela Halfmann, Barbara Dillinger, Fiona Poyer, Katharina Martin, Bernadette Blauensteiner, Maximilian Kauer, Mario Kuttke, Gernot Schabbauer, Alexander M Dohnal

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. MK2 degradation as a sensor of signal intensity that controls stress-induced cell fate.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  4. Article
  5. Article
  6. 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

10 authors at 2 institutions in 1 country.

Klara SoukupTumour Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria. klara.soukup@unil.ch.
Angela HalfmannTumour Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria.
Barbara DillingerTumour Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria.
Fiona PoyerTumour Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria.
Katharina MartinTumour Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria.
Bernadette BlauensteinerTumour Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria.
Maximilian KauerBioinformatics, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria.
Mario KuttkeInstitute for Physiology, Centre for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Gernot SchabbauerInstitute for Physiology, Centre for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Alexander M DohnalTumour Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria. alexander.dohnal@apeiron-biologics.com.
St Anna Children's Hospital · ATMedical University of Vienna · AT

Funding

Austrian Science Fund FWF W 1224
6 · The paper itself

Abstract

Maintaining dendritic cells (DC) in a state of dysfunction represents a key mechanism by which tumour cells evade recognition and elimination by the immune system. Limited knowledge about the intracellular mediators of DC dysfunction restricts success of therapies aimed at reactivating a DC-driven anti-tumour immune response. Using a cell type-specific murine knock-out model, we have identified MAPK-activated protein kinase 2 (MK2) as a major guardian of a suppressive DC phenotype in the melanoma tumour microenvironment. MK2 deletion in CD11c

Indexed as

Immunity, CellularTumor MicroenvironmentAnimalsCD8-Positive T-LymphocytesCell Line, TumorDendritic CellsIntracellular Signaling Peptides and ProteinsMAP-Kinase-Activated Kinase 2Melanoma, ExperimentalMiceMice, KnockoutProtein Serine-Threonine KinasesIntracellular Signaling Peptides and ProteinsMAP-Kinase-Activated Kinase 2Protein Serine-Threonine Kinases

Identifiers

PMID28924177
PMCPMC5603533
OpenAlexW2754687219

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.