Evidence map›Paper›PMID 18473151›Full record

ReviewJournal of mammary gland biology and neoplasia2008

HER4 intracellular domain (4ICD) activity in the developing mammary gland and breast cancer.

Frank E Jones

Open access · greenAbstract readReview
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 102 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Clinicopathologic significance of nuclear HER4 and phospho-YAP(STherapeutic advances in medical oncology · 2020
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
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  19. Article
  20. 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

1 author at 1 institution in 1 country.

Frank E JonesDepartment of Pathology, University of Colorado Health Sciences Center, 12800 East 19th Avenue, Aurora, CO 80045, USA. fjones@tulane.edu
University of Colorado Anschutz Medical Campus · US

Funding

ERBB4 signaling in the normal and neoplastic breastR01CA095783 · NCI · UNIVERSITY OF COLORADO DENVER · PI JONES, FRANK E · 2001 to 2013
$3.4M
Influence of ErbB4 activity on metastatic breast cancerR01CA096717 · NCI · UNIVERSITY OF COLORADO DENVER · PI JONES, FRANK E · 2003 to 2007
$1.8M
NCI NIH HHS CA95783NCI NIH HHS CA96717NCI NIH HHS R01 CA095783NCI NIH HHS R01 CA096717
6 · The paper itself

Abstract

The HER4 receptor tyrosine kinase was the final member of the EGFR-family to be discovered. In contrast to the other three members of this receptor family which function primarily as mitogenic effectors in the breast, HER4 appears to have multiple divergent functions in the normal and malignant breast. Interestingly, the majority of HER4 activities in the breast including pregnancy induced differentiation and lactation initiation, transcriptional activation, tumor cell proliferation, growth suppression, and induction of apoptosis appear to be mediated by an independently signaling soluble HER4 intracellular domain (4ICD). The 4ICD can accumulate within the nucleus or mitochondria and subcellular localization of 4ICD in part determines the physiological response of breast cells to 4ICD action. Here I will discuss the evidence supporting the role of 4ICD as the critical effector of HER4 signaling in the breast. In addition a developmental and temporal model of 4ICD action in the normal breast and during the progression of breast cancer will be presented to explain the paradox of divergent HER4 and 4ICD activities.

Indexed as

AnimalsApoptosisBreast NeoplasmsCell Transformation, NeoplasticErbB ReceptorsFemaleGene Expression RegulationHumansMammary Glands, AnimalMammary Glands, HumanMiceModels, BiologicalProto-Oncogene Proteins c-bcl-2Receptor, ErbB-4Signal TransductionTranscription, GeneticERBB4 protein, humanErbb4 protein, mouseErbB ReceptorsProto-Oncogene Proteins c-bcl-2Receptor, ErbB-4

Identifiers

PMID18473151
PMCPMC2442669
OpenAlexW2001739596

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.