Evidence map›Paper›PMID 12466964›Full record

ArticleOncogene2002

Neuregulin isoforms exhibit distinct patterns of ErbB family receptor activation.

Stuart S Hobbs, Stephanie L Coffing, Ann T D Le, Elizabeth M Cameron, Eric E Williams, Michelle Andrew, Erika N Blommel, Robert P Hammer, Han Chang, David J Riese

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
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

52 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. NRG4-ErbB4 signaling represses proinflammatory macrophage activity.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Article
  12. Development and Validation of a 5-Gene Autophagy-Based Prognostic Index in Endometrial Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
  13. Review
  14. Proteolytic Processing of Neuregulin 2.Molecular neurobiology · 2020
    Article
  15. Article
  16. Article
  17. Article
  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

10 authors.

Stuart S HobbsDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University School of Pharmacy, West Lafayette, Indiana, IN 7907-1333, USA.
Stephanie L Coffing
Ann T D Le
Elizabeth M Cameron
Eric E Williams
Michelle Andrew
Erika N Blommel
Robert P Hammer
Han Chang
David J Riese

Funding

TRAINING IN BIOCHEMISTRY AND MOLECULAR BIOLOGYT32GM008737 · NIGMS · PURDUE UNIVERSITY WEST LAFAYETTE · PI BROYLES, STEVEN S · 1999 to 2003
$495k
TUMOR CELL LINE PROLIFERATION, MOTILITY AND INVASIVENESSR21CA080770 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI RIESE, DAVID J. · 1999 to 2000
$114k
BINDING DETERMINANTS OF NEUREGULIN TO ERB4 RECEPTORF33CA085049 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI HAMMER, ROBERT P · 2000 to 2000
$46k
NCI NIH HHS F33CA085049NCI NIH HHS R21CA080770NIGMS NIH HHS T32GM008737
6 · The paper itself

Abstract

During the last decade, several novel members of the Epidermal Growth Factor family of peptide growth factors have been identified. Most prominent among these are the Neuregulins or Heregulins. To date, four different Neuregulin genes have been identified (Neuregulin1-4) and several different splicing isoforms have been identified for at least two of these genes (Neuregulin1 and Neuregulin2). While Neuregulin1 isoforms have been extensively studied, comparatively little is known about Neuregulin3, Neuregulin4, or the Neuregulin2 isoforms. Indeed, there has been no systematic comparison of the activities of these molecules. Here we demonstrate that Neuregulin2alpha and Neuregulin2beta stimulate ErbB3 tyrosine phosphorylation and coupling to biological responses. In contrast, Neuregulin3 and Neuregulin4 fail to activate ErbB3 signaling. Furthermore, Neuregulin2beta, but not Neuregulin2alpha, stimulates ErbB4 tyrosine phosphorylation and coupling to biological responses. Finally, both Neuregulin3 and Neuregulin4 stimulate modest amounts of ErbB4 tyrosine phosphorylation. However, whereas Neuregulin3 stimulates a modest amount of ErbB4 coupling to biological responses, Neuregulin4 fails to stimulate ErbB4 coupling to biological responses. This suggests that there are qualitative as well as quantitative differences in ErbB family receptor activation by Neuregulin isoforms.

Indexed as

Gene Expression RegulationGenes, erbBAnimalsBase SequenceCell LineCloning, MolecularDNA PrimersDrosophila melanogasterErbB ReceptorsNeuregulinsProtein IsoformsRatsReceptor Protein-Tyrosine KinasesRecombinant ProteinsTransfectionDNA PrimersErbB ReceptorsNeuregulinsProtein IsoformsReceptor Protein-Tyrosine KinasesRecombinant Proteins

Identifiers

PMID12466964

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.