Evidence map›Paper›PMID 32311005›Full record

ArticleThe Journal of cell biology2020

MASTL promotes cell contractility and motility through kinase-independent signaling.

Maria Emilia Taskinen, Elisa Närvä, James R W Conway, Laura Soto Hinojosa, Sergio Lilla, Anja Mai, Nicola De Franceschi, Laura L Elo, Robert Grosse, Sara Zanivan and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. IL-22 regulates MASTL expression in intestinal epithelial cells.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  5. Article
  6. Deficiency ofFrontiers in cell and developmental biology · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. 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

12 authors at 3 institutions in 3 countries.

Maria Emilia TaskinenTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Elisa NärväTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
James R W ConwayTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Laura Soto HinojosaInstitute of Experimental and Clinical Pharmacology and Toxicology, University of Freiburg, and Center for Integrative Biological Signalling Studies, Freiburg, Germany.
Sergio LillaCancer Research UK Beatson Institute, Glasgow, UK.
Anja MaiTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Nicola De FranceschiTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Laura L EloTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Robert GrosseInstitute of Experimental and Clinical Pharmacology and Toxicology, University of Freiburg, and Center for Integrative Biological Signalling Studies, Freiburg, Germany.
Sara ZanivanCancer Research UK Beatson Institute, Glasgow, UK.
Jim C NormanCancer Research UK Beatson Institute, Glasgow, UK.
Johanna IvaskaTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Åbo Akademi University · FICancer Research UK Scotland Institute · GBUniversity of Freiburg · DE

Funding

Cancer Research UK 18277Cancer Research UK 28291Cancer Research UK 29800Cancer Research UK A12935Cancer Research UK A17196European Research Council 615258Medical Research Council MR/P01058X/1
6 · The paper itself

Abstract

Microtubule-associated serine/threonine-protein kinase-like (MASTL) is a mitosis-accelerating kinase with emerging roles in cancer progression. However, possible cell cycle-independent mechanisms behind its oncogenicity remain ambiguous. Here, we identify MASTL as an activator of cell contractility and MRTF-A/SRF (myocardin-related transcription factor A/serum response factor) signaling. Depletion of MASTL increased cell spreading while reducing contractile actin stress fibers in normal and breast cancer cells and strongly impairing breast cancer cell motility and invasion. Transcriptome and proteome profiling revealed MASTL-regulated genes implicated in cell movement and actomyosin contraction, including Rho guanine nucleotide exchange factor 2 (GEF-H1, ARHGEF2) and MRTF-A target genes tropomyosin 4.2 (TPM4), vinculin (VCL), and nonmuscle myosin IIB (NM-2B, MYH10). Mechanistically, MASTL associated with MRTF-A and increased its nuclear retention and transcriptional activity. Importantly, MASTL kinase activity was not required for regulation of cell spreading or MRTF-A/SRF transcriptional activity. Taken together, we present a previously unknown kinase-independent role for MASTL as a regulator of cell adhesion, contractility, and MRTF-A/SRF activity.

Indexed as

Actin CytoskeletonCell AdhesionCell CycleCell Line, TumorCell MovementCell NucleusGene Expression ProfilingHumansIntegrinsMicrotubule-Associated ProteinsNonmuscle Myosin Type IIBPhosphorylationProtein BindingProtein Serine-Threonine KinasesProteomeRho Guanine Nucleotide Exchange FactorsARHGEF2 protein, humanIntegrinsMASTL protein, humanMicrotubule-Associated ProteinsMRTFA protein, humanNonmuscle Myosin Type IIBProtein Serine-Threonine KinasesProteomeRho Guanine Nucleotide Exchange FactorsRNA, Small InterferingTPM4 protein, humanTrans-ActivatorsTropomyosinVCL protein, humanVinculin

Identifiers

PMID32311005
PMCPMC7265322
OpenAlexW3016866391

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.