Evidence map›Paper›PMID 11467454›Full record

ReviewJournal of mammary gland biology and neoplasia2001

Regulation of mouse mammary gland development and tumorigenesis by the ERBB signaling network.

K L Troyer, D C Lee

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.7field-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

47 citing papers in PubMed, 113 citations in OpenAlex.

  1. Review
  2. A Basic Review on Estrogen Receptor Signaling Pathways in Breast Cancer.International journal of molecular sciences · 2023
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Oncology letters · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Deregulation of the Hippo pathway in mouse mammary stem cells promotes mammary tumorigenesis.Mammalian genome : official journal of the International Mammalian Genome Society · 2016
    Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Progressive increase of glucose transporter-3 (GLUT-3) expression in estrogen-induced breast carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2013
    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

2 authors at 1 institution in 1 country.

K L TroyerDepartment of Microbiology Immunology, University of North Carolina at Chapel Hill, 27599-7260, USA.
D C Lee
UNC Lineberger Comprehensive Cancer Center

Funding

REGULATION OF TRANSFORMING GROWTH FACTORSR01CA043793 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUNNARBORG, SUSAN WOHLER · 1987 to 2007
$2.3M
GROWTH FACTOR INDUCED BREAST CANCERR01CA061896 · NCI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI LEE, DAVID C · 1994 to 2004
$1.7M
NCI NIH HHS CA43793NCI NIH HHS CA61896
6 · The paper itself

Abstract

The four ERBB receptors and their multiple polypeptide ligands are differentially expressed during development of the mouse mammary gland. Profiles suggest that ERBB1/EGF receptor (EGFR)4 and ERBB2/Neu are required during ductal morphogenesis, whereas the Neuregulin (NRG) receptors, ERBB3 and ERBB4, are preferentially expressed through alveolar morphogenesis and lactation. Consistent with these profiles, recent gene knockouts established that EGFR and its ligand, Amphiregulin (AR), are essential for ductal morphogenesis in the adolescent mouse and likely provide the required epithelial-stromal signal. In contrast, the phenotypes of transgenic mice expressing dominant negative ERBB2 and ERBB4 proteins suggest that these receptors differentially act to promote or maintain alveolar differentiation. This view of ERBB action provides a conceptual framework for future testing using more sophisticated conditional knockout models. New or existing transgenic mice are also being used to better understand the contributions of ERBB receptors and ligands to mammary tumorigenesis, as well as to more closely mimic the human disease. Recent studies have focused on defining molecular events in neoplastic progression, and in the case of ERBB2/Neu, the requirement for ERBB heterodimerization partners as well as the relative importance of gene amplification versus gene mutation. Collectively, these recent studies establish that normal development and homeostasis of the mammary gland is critically dependent on regulated ERBB signaling. They also illustrate the value of animal models in deciphering roles for the complex ERBB network in this dynamic tissue.

Indexed as

AnimalsErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleGene Expression Regulation, DevelopmentalHumansMammary Glands, AnimalMammary Neoplasms, AnimalMiceSignal TransductionErb-b2 Receptor Tyrosine KinasesErbB Receptors

Identifiers

PMID11467454
OpenAlexW63627267

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.