Evidence map›Paper›PMID 24402051›Full record

ReviewPediatric research2014

ErbB receptors and their growth factor ligands in pediatric intestinal inflammation.

Mark R Frey, D Brent Polk

Open access · bronzeAbstract readReview
In one paragraph

Review in Pediatric research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Network pharmacology andAnnals of medicine · 2022
    Article
  5. Article
  6. NRG4-ErbB4 signaling represses proinflammatory macrophage activity.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. ADAM Proteases and Gastrointestinal Function.Annual review of physiology · 2016
    Review
  13. Article
  14. Article
  15. 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.

Mark R Frey1] Department of Pediatrics, University of Southern California Keck School of Medicine, Los Angeles, California [2] Department of Biochemistry and Molecular Biology, University of Southern California Keck School of Medicine, Los Angeles, California [3] Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California.
D Brent Polk1] Department of Pediatrics, University of Southern California Keck School of Medicine, Los Angeles, California [2] Department of Biochemistry and Molecular Biology, University of Southern California Keck School of Medicine, Los Angeles, California [3] Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California.
University of Southern California · US

Funding

CYTOKINE REGULATION OF INTESTINAL EPITHELIAL RESTITUTIONR01DK056008 · NIDDK · VANDERBILT UNIVERSITY · PI POLK, D BRENT · 1999 to 2020
$6.8M
The role of the ErbB4 and ErbB3 neuregulin receptors in intestinal epithelial regenerationR01DK095004 · NIDDK · CHILDREN'S HOSPITAL OF LOS ANGELES · PI FREY, MARK R · 2013 to 2022
$3.5M
Regulation of cyclooxygenase-2 by ErbB4 in colon epithelial cellsR03DK090295 · NIDDK · CHILDREN'S HOSPITAL OF LOS ANGELES · PI FREY, MARK R · 2011 to 2012
$160k
NIDDK NIH HHS R01 DK056008NIDDK NIH HHS R01DK056008NIDDK NIH HHS R01 DK095004NIDDK NIH HHS R01DK095004NIDDK NIH HHS R03 DK090295NIDDK NIH HHS R03DK090295
6 · The paper itself

Abstract

The ErbB tyrosine kinases (epidermal growth factor receptor (EGFR), ErbB2/HER2, ErbB3, and ErbB4) are cell surface growth factor receptors widely expressed in many developing mammalian tissues, including in the intestinal tract. Signaling elicited by these receptors promotes epithelial cell growth and survival, and ErbB ligands have been proposed as therapeutic agents for intestinal diseases of pediatric populations, including inflammatory bowel disease (IBD), necrotizing enterocolitis (NEC), and inflammation associated with total parenteral nutrition (TPN). Furthermore, emerging evidence points to reduced ErbB ligand expression and thus reduced ErbB activity in IBD, NEC, and TPN models. This review will discuss the current understanding of the role of ErbB receptors in the pathogenesis and potential treatment of pediatric intestinal inflammation, with focus on the altered signaling in disease and the molecular mechanisms by which exogenous ligands are protective.

Indexed as

Signal TransductionAnimalsAnti-Inflammatory AgentsColitisCrohn DiseaseDisease Models, AnimalDrug DesignEnterocolitis, NecrotizingErb-b2 Receptor Tyrosine KinasesErbB ReceptorsGastrointestinal AgentsHumansInflammatory Bowel DiseasesIntestinal MucosaIntestinesLigandsAnti-Inflammatory AgentsEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesERBB3 protein, humanERBB4 protein, humanErbB ReceptorsGastrointestinal AgentsLigandsReceptor, ErbB-3Receptor, ErbB-4

Identifiers

PMID24402051
PMCPMC4005598
OpenAlexW1973656733

What OpenQuestion holds

Textmetadata
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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.