Evidence map›Paper›PMID 26774483›Full record

ArticleCell reports2016

Knockout of the PKN Family of Rho Effector Kinases Reveals a Non-redundant Role for PKN2 in Developmental Mesoderm Expansion.

Ivan Quétier, Jacqueline J T Marshall, Bradley Spencer-Dene, Sylvie Lachmann, Adele Casamassima, Claudio Franco, Sarah Escuin, Joseph T Worrall, Priththivika Baskaran, Vinothini Rajeeve and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  7. Role of PKN1 in Retinal Cell Type Formation.International journal of molecular sciences · 2024
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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

18 authors at 6 institutions in 3 countries.

Ivan QuétierKinase Biology Laboratory, John Vane Science Centre, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
Jacqueline J T MarshallProtein Phosphorylation Laboratory, Francis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.
Bradley Spencer-DeneFrancis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.
Sylvie LachmannProtein Phosphorylation Laboratory, Francis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.
Adele CasamassimaProtein Phosphorylation Laboratory, Francis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.
Claudio FrancoInstituto Medicina Molecular (iMM), Faculdade de Medicina da Universidade de Lisboa, 1649-028 Lisbon, Portugal.
Sarah EscuinNewlife Birth Defects Research Centre, Institute of Child Health, University College, London WC1N 1EH, UK.
Joseph T WorrallJohn Vane Science Centre, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
Priththivika BaskaranKinase Biology Laboratory, John Vane Science Centre, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
Vinothini RajeeveJohn Vane Science Centre, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
Michael HowellFrancis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.
Andrew J CoppNewlife Birth Defects Research Centre, Institute of Child Health, University College, London WC1N 1EH, UK.
Gordon StampFrancis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.
Ian RosewellGenetic Manipulation Services, Francis Crick Institute, Clare Hall, Herts EN6 3LD, UK.
Pedro CutillasJohn Vane Science Centre, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
Holger GerhardtMax-Delbrück-Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Peter J ParkerProtein Phosphorylation Laboratory, Francis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK; Division of Cancer Studies, King's College London, New Hunt's House, Saint Thomas Street, London SE1 1UL, UK. Electronic address: peter.parker@crick.ac.uk.
Angus J M CameronKinase Biology Laboratory, John Vane Science Centre, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK. Electronic address: a.cameron@qmul.ac.uk.
Queen Mary University of London · GBThe Honourable Society of Lincoln's Inn · GBThe Francis Crick Institute · GBUniversity College London · GBMax Delbrück Center · DEUniversity of Lisbon · PT

Funding

Cancer Research UK 15683Medical Research Council G0801124Wellcome Trust 087525
6 · The paper itself

Abstract

In animals, the protein kinase C (PKC) family has expanded into diversely regulated subgroups, including the Rho family-responsive PKN kinases. Here, we describe knockouts of all three mouse PKN isoforms and reveal that PKN2 loss results in lethality at embryonic day 10 (E10), with associated cardiovascular and morphogenetic defects. The cardiovascular phenotype was not recapitulated by conditional deletion of PKN2 in endothelial cells or the developing heart. In contrast, inducible systemic deletion of PKN2 after E7 provoked collapse of the embryonic mesoderm. Furthermore, mouse embryonic fibroblasts, which arise from the embryonic mesoderm, depend on PKN2 for proliferation and motility. These cellular defects are reflected in vivo as dependence on PKN2 for mesoderm proliferation and neural crest migration. We conclude that failure of the mesoderm to expand in the absence of PKN2 compromises cardiovascular integrity and development, resulting in lethality.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell LineCell MovementCell ProliferationEmbryo, MammalianEmbryonic DevelopmentGenes, ReporterHeartMesodermMiceMice, Inbred C57BLMice, KnockoutMicroscopy, Electron, ScanningMyocardiumafimoxifeneAntineoplastic AgentsProtein Kinase Cprotein kinase NTamoxifen4-hydroxytamoxifen4-OHTEmbryonic stem cellsES cellsMEFmouse embryonic fibroblastsNCCsneural crest cellsPKCPKNprotein kinase CProtein kinase N

Identifiers

PMID26774483
PMCPMC4733087
OpenAlexW2228137772

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.