Evidence map›Paper›PMID 30249613›Full record

ArticleMolecular pharmacology2018

Betacellulin (BTC) Biases the EGFR To Dimerize with ErbB3.

Jamie S Rush, Joanne L Peterson, Brian P Ceresa

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Regulation of receptor tyrosine kinase hetero-interactions.Current opinion in structural biology · 2025
    Review
  3. Article
  4. Article
  5. [Risk modeling based on HER-2 related genes for bladder cancer survival prognosis assessment].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Association of Key Genes and Pathways with Atopic Dermatitis by Bioinformatics Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2019
    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

3 authors at 1 institution in 1 country.

Jamie S RushDepartments of Pharmacology and Toxicology (J.S.R., J.L.P., B.P.C.) and Visual Science (B.P.C.), University of Louisville, Louisville, Kentucky.
Joanne L PetersonDepartments of Pharmacology and Toxicology (J.S.R., J.L.P., B.P.C.) and Visual Science (B.P.C.), University of Louisville, Louisville, Kentucky.
Brian P CeresaDepartments of Pharmacology and Toxicology (J.S.R., J.L.P., B.P.C.) and Visual Science (B.P.C.), University of Louisville, Louisville, Kentucky brian.ceresa@louisville.edu.
University of Louisville · US

Funding

Modulation of EGFR Signaling to Promote Corneal Epithelial Wound HealingR01EY021497 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CERESA, BRIAN P. · 2012 to 2014
$1.0M
Identifying novel c-Cbl antagonists to promote corneal epithelial regenerationR21EY027032 · NEI · UNIVERSITY OF LOUISVILLE · PI CERESA, BRIAN P. · 2016 to 2017
$424k
NEI NIH HHS R01 EY021497NEI NIH HHS R21 EY027032
6 · The paper itself

Abstract

There are 13 known endogenous ligands for the epidermal growth factor receptor (EGFR) and its closely related ErbB receptor family members. We previously reported that betacellulin (BTC) is more efficacious than epidermal growth factor (EGF) in mediating corneal wound healing, although the molecular basis for this difference was unknown. For the most part, differences between ligands can be attributed to variability in binding properties, such as the unique rate of association and dissociation, pH sensitivity, and selective binding to individual ErbB family members of each ligand. However, this was not the case for BTC. Despite being better at promoting wound healing via enhanced cell migration, BTC has reduced receptor affinity and weaker induction of EGFR phosphorylation. These data indicate that the response of BTC is not due to enhanced affinity or kinase activity. Receptor phosphorylation and proximity ligation assays indicate that BTC treatment significantly increases ErbB3 phosphorylation and EGFR-ErbB3 heterodimers when compared with EGF treatment. We observed that EGFR-ErbB3 heterodimers contribute to cell migration, because the addition of an ErbB3 antagonist (MM-121) or RNA interference-mediated knockdown of ErbB3 attenuates BTC-stimulated cell migration compared with EGF. Thus, we demonstrate that, despite both ligands binding to the EGFR, BTC biases the EGFR to dimerize with ErbB3 to regulate the biologic response.

Indexed as

BetacellulinCell LineCell MovementEpidermal Growth FactorErbB ReceptorsHumansLigandsPhosphorylationReceptor, ErbB-3Signal TransductionBetacellulinBTC protein, humanEGFR protein, humanEpidermal Growth FactorERBB3 protein, humanErbB ReceptorsLigandsReceptor, ErbB-3

Identifiers

PMID30249613
PMCPMC6207915
OpenAlexW2894017407

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.