Evidence map›Paper›PMID 22430756›Full record

ReviewSeminars in cell & developmental biology2012

What is bad in cancer is good in the embryo: importance of EMT in neural crest development.

Laura Kerosuo, Marianne Bronner-Fraser

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

70 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
  2. A dual role for GLI3 signaling in neural crest development.Development (Cambridge, England) · 2026
    Article
  3. Article
  4. Article
  5. From neural crest migration to the onset of gangliogenesis.Current topics in developmental biology · 2025
    Review
  6. Review
  7. Article
  8. Tissue Morphogenesis Through Dynamic Cell and Matrix Interactions.Annual review of cell and developmental biology · 2023
    Review
  9. Article
  10. Genes · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Biallelic Mutations inFrontiers in cell and developmental biology · 2021
    Article
  20. Article

10 more citing papers are in PubMed but not listed here.

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.

Laura KerosuoDivision of Biology, California Institute of Technology, Pasadena, CA 91125, United States.
Marianne Bronner-Fraser
California Institute of Technology · US

Funding

Transcriptional Casualty in Embryonic Morphogenesis: from the Specifications GRNP01HD037105 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI DAVIDSON, ERIC H · 1999 to 2018
$27.1M
Ectodermal Placode Development into Sensory StructuresR01DE016459 · NIDCR · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE · 2004 to 2014
$3.8M
Evolutionary Origin of Vertebrate Neural Crest Gene NetworksR01DE017911 · NIDCR · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE · 2007 to 2011
$2.7M
Gene regulatory network controlling commitment to ear identityR01DC011577 · NIDCD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE, STREIT, ANDREA · 2012 to 2016
$2.6M
NICHD NIH HHS HD037105NICHD NIH HHS P01 HD037105NIDCD NIH HHS R01 DC011577NIDCR NIH HHS DE017911NIDCR NIH HHS R01 DE016459NIDCR NIH HHS R01 DE017911
6 · The paper itself

Abstract

Although the epithelial to mesenchymal transition (EMT) is famous for its role in cancer metastasis, it also is a normal developmental event in which epithelial cells are converted into migratory mesenchymal cells. A prime example of EMT during development occurs when neural crest (NC) cells emigrate from the neural tube thus providing an excellent model to study the principles of EMT in a nonmalignant environment. NC cells start life as neuroepithelial cells intermixed with precursors of the central nervous system. After EMT, they delaminate and begin migrating, often to distant sites in the embryo. While proliferating and maintaining multipotency and cell survival the transitioning neural crest cells lose apicobasal polarity and the basement membrane is broken down. This review discusses how these events are coordinated and regulated, by series of events involving signaling factors, gene regulatory interactions, as well as epigenetic and post-transcriptional modifications. Even though the series of events involved in NC EMT are well known, the sequence in which these steps take place remains a subject of debate, raising the intriguing possibility that, rather than being a single event, neural crest EMT may involve multiple parallel mechanisms.

Indexed as

AnimalsCell MovementEpithelial CellsEpithelial-Mesenchymal TransitionHumansMesodermNeoplasmsNeural Crest

Identifiers

PMID22430756
PMCPMC3345076
OpenAlexW2018580411

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.