Evidence map›Paper›PMID 29330906›Full record

ReviewGenesis (New York, N.Y. : 2000)2018

Generating retinoic acid gradients by local degradation during craniofacial development: One cell's cue is another cell's poison.

Aditi Dubey, Rebecca E Rose, Drew R Jones, Jean-Pierre Saint-Jeannet

Open access · greenAbstract readReview
In one paragraph

Review in Genesis (New York, N.Y. : 2000), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 41 citations in OpenAlex.

  1. Retinoic acid in health and disease.Signal transduction and targeted therapy · 2026
    Review
  2. A novelFrontiers in cell and developmental biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Pet Wellness and Vitamin A: A Narrative Overview.Animals : an open access journal from MDPI · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Biology · 2023
    Article
  11. Review
  12. Anterior patterning genes induced by Zic1 are sensitive to retinoic acid and its metabolite, 4-oxo-RA.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Role of carotenoids and retinoids during heart development.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    Review
  18. Article
  19. Review
  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

4 authors at 2 institutions in 1 country.

Aditi DubeyDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, New York.
Rebecca E RoseDepartment of Biochemistry and Molecular Pharmacology, New York University Langone Health, New York, New York.
Drew R JonesDepartment of Biochemistry and Molecular Pharmacology, New York University Langone Health, New York, New York.
Jean-Pierre Saint-JeannetDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, New York.ORCID 0000-0003-3259-2103
New York University · USNYU Langone Health · US

Funding

Pathogenesis of craniofacial defects in Nager syndromeR01DE025468 · NIDCR · NEW YORK UNIVERSITY · PI SAINT-JEANNET, JEAN-PIERRE · 2016 to 2020
$2.0M
Molecular control of cranial placode progenitor formationR01DE025806 · NIDCR · NEW YORK UNIVERSITY · PI SAINT-JEANNET, JEAN-PIERRE · 2016 to 2020
$2.0M
NIDCR NIH HHS R01 DE025468NIDCR NIH HHS R01 DE025806
6 · The paper itself

Abstract

Retinoic acid (RA) is a vital morphogen for early patterning and organogenesis in the developing embryo. RA is a diffusible, lipophilic molecule that signals via nuclear RA receptor heterodimeric units that regulate gene expression by interacting with RA response elements in promoters of a significant number of genes. For precise RA signaling, a robust gradient of the morphogen is required. The developing embryo contains regions that produce RA, and specific intracellular concentrations of RA are created through local degradation mediated by Cyp26 enzymes. In order to elucidate the mechanisms by which RA executes precise developmental programs, the kinetics of RA metabolism must be clearly understood. Recent advances in techniques for endogenous RA detection and quantification have paved the way for mechanistic studies to shed light on downstream gene expression regulation coordinated by RA. It is increasingly coming to light that RA signaling operates not only at precise concentrations but also employs mechanisms of degradation and feedback inhibition to self-regulate its levels. A global gradient of RA throughout the embryo is often found concurrently with several local gradients, created by juxtaposed domains of RA synthesis and degradation. The existence of such local gradients has been found especially critical for the proper development of craniofacial structures that arise from the neural crest and the cranial placode populations. In this review, we summarize the current understanding of how local gradients of RA are established in the embryo and their impact on craniofacial development.

Indexed as

Cell CommunicationFetal DevelopmentOrganogenesisAnimalsBiomarkersCatalysisCytochrome P450 Family 26Gene Expression Regulation, DevelopmentalHumansKineticsMorphogenesisNeural CrestSignal TransductionSkullTretinoinBiomarkersCytochrome P450 Family 26TretinoincraniofacialCyp26degradationgradientneural crestplacodeRaldhretinoic acid

Identifiers

PMID29330906
PMCPMC5818312
OpenAlexW2783054487

What OpenQuestion holds

Textmetadata
LicenceTDM
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.