Evidence map›Paper›PMID 30782830›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase.

Michaela Kunova Bosakova, Alexandru Nita, Tomas Gregor, Miroslav Varecha, Iva Gudernova, Bohumil Fafilek, Tomas Barta, Neha Basheer, Sara P Abraham, Lukas Balek and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Ciliary-Mediated Mechanotransduction in Skeletal Development and Diseases.Results and problems in cell differentiation · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. FGF-based drug discovery: advances and challenges.Nature reviews. Drug discovery · 2025
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Illumination of understudied ciliary kinases.Frontiers in molecular biosciences · 2024
    Review
  18. Article
  19. Article
  20. 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

28 authors at 7 institutions in 4 countries.

Michaela Kunova BosakovaDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.ORCID 0000-0002-7627-0344
Alexandru NitaDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Tomas GregorCentral European Institute of Technology, Masaryk University, 62500 Brno, Czech Republic.
Miroslav VarechaDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Iva GudernovaDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Bohumil FafilekDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Tomas BartaDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Neha BasheerDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Sara P AbrahamDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Lukas BalekDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Marketa TomanovaDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Jana Fialova KucerovaDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Juraj BosakDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
David PotesilCentral European Institute of Technology, Masaryk University, 62500 Brno, Czech Republic.
Jennifer ZiebaDepartment of Orthopaedic Surgery, David Geffen School of Medicine University of California, Los Angeles, CA 90095.
Jieun SongDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, 03722 Seoul, Korea.
Peter KonikInstitute of Chemistry and Biochemistry, Faculty of Science, University of South Bohemia, 37005 Ceske Budejovice, Czech Republic.ORCID 0000-0001-8652-5323
Sohyun ParkDepartment of Pharmacology, University of Virginia School of Medicine, Charlottesville, VA 22908.
Ivan DuranDepartment of Orthopaedic Surgery, David Geffen School of Medicine University of California, Los Angeles, CA 90095.ORCID 0000-0001-6097-0402
Zbynek ZdrahalCentral European Institute of Technology, Masaryk University, 62500 Brno, Czech Republic.
David SmajsDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Gert JansenDepartment of Cell Biology, Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands.ORCID 0000-0002-7524-171X
Zheng FuDepartment of Pharmacology, University of Virginia School of Medicine, Charlottesville, VA 22908.
Hyuk Wan KoDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, 03722 Seoul, Korea.ORCID 0000-0003-1753-1900
Ales HamplInternational Clinical Research Center, St. Anne's University Hospital, 65691 Brno, Czech Republic.
Lukas TrantirekCentral European Institute of Technology, Masaryk University, 62500 Brno, Czech Republic.
Deborah KrakowDepartment of Orthopaedic Surgery, David Geffen School of Medicine University of California, Los Angeles, CA 90095; dkrakow@mednet.ucla.edu krejcip@med.muni.cz.ORCID 0000-0001-9906-4968
Pavel KrejciDepartment of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic; dkrakow@mednet.ucla.edu krejcip@med.muni.cz.
Masaryk University · CZCentral European Institute of Technology · CZUniversity of California, Los Angeles · USUniversity of Virginia · USYonsei University · KRErasmus MC · NLUniversity of South Bohemia in České Budějovice · CZ

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Short-rib polydactyly and the skeletal ciliopathiesR01DE019567 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COHN, DANIEL H, KRAKOW, DEBORAH · 2009 to 2019
$3.5M
Signaling Mechanisms and Cellular Functions of a Ciliopathy-Associated Protein KinaseR01GM127690 · NIGMS · UNIVERSITY OF VIRGINIA · PI Zheng Fu · 2018 to 2026
$2.4M
Exome sequencing in the skeletal dysplasiasR01AR062651 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COHN, DANIEL H · 2013 to 2017
$1.7M
Unraveling the mechanisms of prenatal-onset disorders affecting the skeletonR01AR066124 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KRAKOW, DEBORAH · 2014 to 2018
$1.7M
Oncogenic role of the ICK-GSK3beta signaling pathwayR21CA195273 · NCI · UNIVERSITY OF VIRGINIA · PI FU, ZHENG · 2016 to 2017
$378k
NCATS NIH HHS UL1 TR000124NCI NIH HHS R21 CA195273NIAMS NIH HHS R01 AR062651NIAMS NIH HHS R01 AR066124NIDCR NIH HHS R01 DE019567NIGMS NIH HHS R01 GM127690
6 · The paper itself

Abstract

Vertebrate primary cilium is a Hedgehog signaling center but the extent of its involvement in other signaling systems is less well understood. This report delineates a mechanism by which fibroblast growth factor (FGF) controls primary cilia. Employing proteomic approaches to characterize proteins associated with the FGF-receptor, FGFR3, we identified the serine/threonine kinase intestinal cell kinase (ICK) as an FGFR interactor. ICK is involved in ciliogenesis and participates in control of ciliary length. FGF signaling partially abolished ICK's kinase activity, through FGFR-mediated ICK phosphorylation at conserved residue Tyr15, which interfered with optimal ATP binding. Activation of the FGF signaling pathway affected both primary cilia length and function in a manner consistent with cilia effects caused by inhibition of ICK activity. Moreover, knockdown and knockout of ICK rescued the FGF-mediated effect on cilia. We provide conclusive evidence that FGF signaling controls cilia via interaction with ICK.

Indexed as

AnimalsCiliaCRISPR-Cas SystemsFibroblast Growth FactorsHedgehog ProteinsHEK293 CellsHumansMiceMice, KnockoutModels, AnimalMolecular Docking SimulationNIH 3T3 CellsPhosphorylationProtein Interaction Domains and MotifsProtein Serine-Threonine KinasesProteomicsCILK1 protein, humanCilk1 protein, mouseFGFR1 protein, humanFGFR3 protein, humanFGFR4 protein, humanFibroblast Growth FactorsHedgehog ProteinsProtein Serine-Threonine KinasesReceptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 3Receptor, Fibroblast Growth Factor, Type 4Receptors, Fibroblast Growth Factorcilia lengthFGFRfibroblast growth factorICKintestinal cell kinase

Identifiers

PMID30782830
PMCPMC6410813
OpenAlexW2918072646

What Socratic holds

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LicenceCC BY-NC-ND
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 Socratic graph.