Evidence map›Paper›PMID 9312048›Full record

ArticleThe EMBO journal1997

Src and Ras are involved in separate pathways in epithelial cell scattering.

B Boyer, S Roche, M Denoyelle, J P Thiery

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.1field-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

41 citing papers in PubMed, 139 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Adherens Junctions on the Move-Membrane Trafficking of E-Cadherin.Cold Spring Harbor perspectives in biology · 2017
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. The role of MAPK in drug-induced kidney injury.Journal of signal transduction · 2012
    Article
  13. Implication of stem cells in the biology and therapy of head and neck cancer.GMS current topics in otorhinolaryngology, head and neck surgery · 2011
    Article
  14. SRC: a century of science brought to the clinic.Neoplasia (New York, N.Y.) · 2010
    Review
  15. Article
  16. Article
  17. Lipocalin 2 promotes breast cancer progression.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  18. Article
  19. Review
  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

4 authors at 3 institutions in 1 country.

B BoyerLaboratoire de Compartimentation et Dynamique cellulaires, UMR CNRS 144, Institut Curie Section de Recherche, 26 rue d'Ulm F-75248 Paris Cedex 05, France. bboyer@curie.fr
S Roche
M Denoyelle
J P Thiery
Centre National de la Recherche Scientifique · FRBiologie cellulaire et Cancer · FRInstitut Curie · FR

Funding

MULTIFUNCTIONAL GROWTH FACTORS IN TUMOR PROGRESSIONR01CA049417 · NCI · NATIONAL CENTER FOR SCIENTIFIC RESEARCH · PI THIERY, JEAN P · 1990 to 1995
–
NCI NIH HHS 2 RO1 CA 49417-06
6 · The paper itself

Abstract

We have demonstrated previously that Src controls the epidermal growth factor (EGF)-induced dispersion of NBT-II carcinoma epithelial cells. Here we show that while only Src and Yes were expressed and activated by EGF, microinjected kinase-inactive mutants of Src (SrcK-) and Fyn (FynK-) were able to exert a dominant-negative effect on the scattering response. Both SH2 and SH3 domains of FynK- were required for inhibition of cell scattering. Expression of dominant-negative N17Ras also abrogated EGF-induced dispersion, showing that Ras is another regulator of cell dispersion. Expression of SrcK- did not alter EGF-evoked Shc tyrosine phosphorylation, Shc-Grb2 complex formation and MAPK activation, three elements of the Ras pathway. Furthermore, the expression of Jun-Fos and Slug rescued the block induced by N17Ras but not by SrcK-, showing that Src kinases and Ras operate in separate pathways. In addition, actinomycin D inhibition of RNA synthesis repressed the ability of the activated mutant L61Ras but not that of F527Src to induce epithelial cell scattering. Since tyrosine phosphorylation of cytoskeleton-associated proteins pp125FAK and cortactin were abolished in EGF-stimulated SrcK- cells, we concluded that, in contrast to Ras, Src kinases may control epithelial cell dispersion in the absence of gene expression and by directly regulating the organization of the cortical cytoskeleton.

Indexed as

AnimalsCell LineCell MovementCSK Tyrosine-Protein KinaseDactinomycinDogsEpidermal Growth FactorEpithelial CellsNucleic Acid Synthesis InhibitorsProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-fynras ProteinsRNASignal Transductionsrc-Family KinasesCSK Tyrosine-Protein KinaseDactinomycinEpidermal Growth FactorNucleic Acid Synthesis InhibitorsProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-fynras ProteinsRNAsrc-Family KinasesTranscription Factors

Identifiers

PMID9312048
PMCPMC1170221
OpenAlexW2032103583

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.