Evidence map›Paper›PMID 11039900›Full record

ArticleOncogene2000

Adhesion induced expression of the serine/threonine kinase Fnk in human macrophages.

U Holtrich, G Wolf, J Yuan, J Bereiter-Hahn, T Karn, M Weiler, G Kauselmann, M Rehli, R Andreesen, M Kaufmann and 2 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

28 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. CIB1: a small protein with big ambitions.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Review
  11. Article
  12. Article
  13. Review
  14. Mitotic Kinases and p53 Signaling.Biochemistry research international · 2012
    Article
  15. Article
  16. Article
  17. Review
  18. Polo-like kinase 3 is required for entry into S phase.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  19. Polo-like kinase isoforms in breast cancer: expression patterns and prognostic implications.Virchows Archiv : an international journal of pathology · 2005
    Article
  20. 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 1 country.

U HoltrichDepartment of Obstetrics and Gynecology, J.W. Goethe-University, Frankfurt, Germany.
G Wolf
J Yuan
J Bereiter-Hahn
T Karn
M Weiler
G Kauselmann
M Rehli
R Andreesen
M Kaufmann
D Kuhl
K Strebhardt
Goethe University Frankfurt · DEUniversität Hamburg · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Members of the polo subfamily of protein kinases play crucial roles in cell proliferation. To study the function of this family in more detail, we isolated the cDNA of human Fnk (FGF-inducible kinase) which codes for a serine/threonine kinase of 646 aa. Despite the homology to the proliferation-associated polo-like kinase (Plk), tissue distribution of Fnk transcripts and expression kinetics differed clearly. In contrast to Plk no correlation between cell proliferation and Fnk gene expression was found. Instead high levels of Fnk mRNA were detectable in blood cells undergoing adhesion. The transition of monocytes from peripheral blood to matrix bound macrophages was accompanied by increasing levels of Fnk with time in culture. Neither treatment of monocytes with inducers of differentiation nor withdrawal of serum did influence Fnk mRNA levels significantly, suggesting that cell attachment triggers the onset of Fnk gene transcription. The idea that Fnk is part of the signalling network controlling cellular adhesion was supported by the analysis of the cytoplasmic distribution of the Fnk protein and the influence of its overexpression on the cellular architecture. Fnk as fusion protein with GFP localized at the cellular membrane in COS cells. Dysregulated Fnk gene expression disrupted the cellular f-actin network and induced a spherical morphology. Furthermore, Fnk binds to the Ca2+/integrin-binding protein Cib in two-hybrid-analyses and co-immunoprecipitation in assays. Moreover, both proteins were shown to co-localize in mammalian cells. The homology of Cib with calmodulin and with calcineurin B suggests that Cib might be a regulatory subunit of polo-like kinases.

Indexed as

Calcium-Binding ProteinsActinsAdultAnimalsBlood CellsCalcineurinCalciumCalmodulinCarrier ProteinsCell AdhesionCell Cycle ProteinsCell DifferentiationCell MembraneChlorocebus aethiopsCOS CellsCulture MediaActinsCalcineurinCalciumCalcium-Binding ProteinsCalmodulinCarrier ProteinsCell Cycle ProteinsCIB1 protein, humanCib1 protein, mouseCulture MediaCulture Media, Serum-FreeDNA, ComplementaryPLK3 protein, humanPolo-Like Kinase 1Polo-like KinasesProtein KinasesProtein Serine-Threonine KinasesProto-Oncogene ProteinsRecombinant Fusion ProteinsRNA, MessengerTumor Suppressor Proteins

Identifiers

PMID11039900
OpenAlexW2065243832

What OpenQuestion holds

Textmetadata
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.