Evidence map›Paper›PMID 22144690›Full record

ArticleThe Journal of cell biology2011

Eph receptor function is modulated by heterooligomerization of A and B type Eph receptors.

Peter W Janes, Bettina Griesshaber, Lakmali Atapattu, Eva Nievergall, Linda L Hii, Anneloes Mensinga, Chanly Chheang, Bryan W Day, Andrew W Boyd, Philippe I Bastiaens and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

64 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Eph receptor signaling complexes in the plasma membrane.Trends in biochemical sciences · 2024
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Investigating the effects of compound paralogous EPHB receptor mutations on mouse facial development.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Eph Receptors and Ephrins in Retinal Diseases.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Down-regulation of HCP5 inhibits cell proliferation, migration, and invasion through regulating EPHA7 by competitively binding miR-101 in osteosarcoma.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
    Article
  18. Article
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 3 countries.

Peter W JanesDepartment of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia.
Bettina Griesshaber
Lakmali Atapattu
Eva Nievergall
Linda L Hii
Anneloes Mensinga
Chanly Chheang
Bryan W Day
Andrew W Boyd
Philippe I Bastiaens
Claus Jørgensen
Tony Pawson
Martin Lackmann
Monash University · AULunenfeld-Tanenbaum Research Institute · CAQIMR Berghofer Medical Research Institute · AUMax Planck Institute of Molecular Physiology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eph receptors interact with ephrin ligands on adjacent cells to facilitate tissue patterning during normal and oncogenic development, in which unscheduled expression and somatic mutations contribute to tumor progression. EphA and B subtypes preferentially bind A- and B-type ephrins, respectively, resulting in receptor complexes that propagate via homotypic Eph-Eph interactions. We now show that EphA and B receptors cocluster, such that specific ligation of one receptor promotes recruitment and cross-activation of the other. Remarkably, coexpression of a kinase-inactive mutant EphA3 with wild-type EphB2 can cause either cross-activation or cross-inhibition, depending on relative expression. Our findings indicate that cellular responses to ephrin contact are determined by the EphA/EphB receptor profile on a given cell rather than the individual Eph subclass. Importantly, they imply that in tumor cells coexpressing different Ephs, functional mutations in one subtype may cause phenotypes that are a result of altered signaling from heterotypic rather from homotypic Eph clusters.

Indexed as

PolymerizationAnimalsCell Line, TumorChlorocebus aethiopsCOS CellsGliomaHEK293 CellsHumansMaleProstatic NeoplasmsReceptors, Eph FamilySignal TransductionReceptors, Eph Family

Identifiers

PMID22144690
PMCPMC3241718
OpenAlexW2045346771

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.