Evidence map›Paper›PMID 10882304›Full record

ReviewJournal of mammary gland biology and neoplasia1997

Roles of ErbB-3 and ErbB-4 in the physiology and pathology of the mammary gland.

K L Carraway, C A Carraway, K L Carraway

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 1997. 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
2.2field-weighted citation impact, top 11% 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, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The ErbB receptors as targets for breast cancer therapy.Journal of mammary gland biology and neoplasia · 1999
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. EGF-related peptides and their receptors in mammary gland development.Journal of mammary gland biology and neoplasia · 1997
    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

3 authors at 2 institutions in 1 country.

K L CarrawayDepartment of Cell Biology and Anatomy, University of Miami School of Medicine, Florida 33101, USA. Kcarrawa@mednet.med.miami.edu
C A Carraway
K L Carraway
University of Miami · USHarvard University · US

Funding

STRUCTURE/BIOSYNTHESIS OF TUMOR SIALOMUCIN COMPLEXR01CA052498 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CARRAWAY, KERMIT L. · 1991 to 2009
$2.7M
CORE--WORD PROCESSING CENTERP30CA014395 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · 1985 to 1995
–
NCI NIH HHS CA14395NCI NIH HHS CA52498
6 · The paper itself

Abstract

ErbB-3 and ErbB-4 are the most recently discovered and least characterized of the class I tyrosine kinase receptors. ErbB-3 is noteworthy for its low tyrosine kinase activity, suggesting that it may function more as an adaptor in signaling than as a kinase. Heregulin serves as a ligand for both receptors. A primary mechanism of heregulin action involves heterodimerization of its targeted receptors with other members of the class I family to promote cross-phosphorylation and cellular responses. Betacellulin also acts as a ligand for ErbB-4 to stimulate its kinase activity in both homo- and hetero-dimers. A new ligand (ASGP-2) for ErbB-2 has been discovered which operates by an intramembrane mechanism and may be able to modulate external ligand-dependent ErbB-3 or ErbB-4 heterodimeric interactions with ErbB-2. Heterodimerization stimulated by the ligands is a key feature of mitogenic signaling in mammary epithelial cells and tumors. Characterization of the signaling pathways for these receptors is still incomplete, but phosphatidylinositol 3-kinase and SHC have been implicated. Heregulin synthesized by the mesenchyme has been implicated in mammary development, modulated by systemic hormones. Observations on cultured mammary cells and mammary tumors have suggested linkages of ErbB-3 and ErbB-4 to proliferation and differentiation, respectively, but further work is needed to establish their definitive roles.

Indexed as

AnimalsBreastBreast NeoplasmsDimerizationErbB ReceptorsFemaleHumansMammary Glands, AnimalReceptor, ErbB-3Receptor, ErbB-4Signal TransductionERBB4 protein, humanErbB ReceptorsReceptor, ErbB-3Receptor, ErbB-4

Identifiers

PMID10882304
OpenAlexW2409820727

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.