Evidence map›Paper›PMID 24966332›Full record

ArticleThe Journal of biological chemistry2014

Hypoxia-inducible factor-1α induces ErbB4 signaling in the differentiating mammary gland.

Ilkka Paatero, Tiffany N Seagroves, Katri Vaparanta, Wen Han, Frank E Jones, Randall S Johnson, Klaus Elenius

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer.Journal of experimental & clinical cancer research : CR · 2020
    Review
  3. Review
  4. Article
  5. Article
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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

7 authors at 4 institutions in 3 countries.

Ilkka PaateroFrom the Department of Medical Biochemistry and Genetics, and MediCity Research Laboratory, University of Turku, 20520 Turku, Finland, the Turku Graduate School of Biomedical Sciences, 20520 Turku, Finland.
Tiffany N Seagrovesthe Department of Pathology and Laboratory Medicine, University of Tennessee Health Science Center, Memphis, Tennessee 38163.
Katri VaparantaFrom the Department of Medical Biochemistry and Genetics, and MediCity Research Laboratory, University of Turku, 20520 Turku, Finland.
Wen Hanthe Department of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana 70118.
Frank E Jonesthe Department of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana 70118.
Randall S Johnsonthe Department of Physiology, Development & Neuroscience, University of Cambridge, Cambridge CB2 1TN, United Kingdom, and.
Klaus EleniusFrom the Department of Medical Biochemistry and Genetics, and MediCity Research Laboratory, University of Turku, 20520 Turku, Finland, the Department of Oncology, Turku University Hospital, 20520 Turku, Finland klaus.elenius@utu.fi.
University of Turku · FITulane University · USUniversity of Cambridge · GBUniversity of Tennessee Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conditional knock-out of Hif1a in the mouse mammary gland impairs lobuloalveolar differentiation during lactation. Here, we demonstrate that expression of ErbB4 was reduced in the lobulalveoli of mice with mammary gland-specific deletion of Hif1a. Erbb4 was not, however, a direct target gene for transcriptional regulation by HIF-1α in vitro. HIF-1α overexpression or HIF accumulating prolyl hydroxylase inhibitors reduced ErbB4 endocytosis, promoted transcriptional co-regulatory activity of ErbB4, and stimulated ErbB4-induced differentiation of mammary carcinoma cells. Consistently, RNA interference-mediated down-regulation of HIF-1α resulted in reduced ErbB4 protein amount and reduced mammary carcinoma cell differentiation. These findings indicate that HIF-1α is a physiologically relevant regulator of ErbB4 and that ErbB4 is involved in HIF-regulated differentiation of the mammary gland.

Indexed as

AnimalsCell DifferentiationCell Line, TumorEndocytosisFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitLactationMammary Glands, AnimalMammary Glands, HumanMiceMice, KnockoutPeptide FragmentsPregnancyReceptor, ErbB-4Signal TransductionERBB4 protein, humanErbb4 protein, mouseHIF1A protein, humanHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitPeptide FragmentsReceptor, ErbB-4Cell SignalingEpidermal Growth Factor Receptor (EGFR)ErbB4Growth FactorHypoxia-inducible Factor (HIF)LactationMammary GlandReceptor Tyrosine KinaseSignal Transduction

Identifiers

PMID24966332
PMCPMC4139252
OpenAlexW1980911789

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.