Evidence map›Paper›PMID 17587819›Full record

ReviewCells, tissues, organs2007

Complexity in interpretation of embryonic epithelial-mesenchymal transition in response to transforming growth factor-beta signaling.

Shaheen Ahmed, Ali Nawshad

Open access · bronzeAbstract readReview
In one paragraph

Review in Cells, tissues, organs, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Anticancer Activity ofNutrients · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. The microRNA networks of TGFβ signaling in cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Review
  9. The role of microRNAs in prostate cancer progression.Translational andrology and urology · 2013
    Review
  10. Article
  11. Article
  12. Article
  13. Ligand-specific function of transforming growth factor beta in epithelial-mesenchymal transition in heart development.Developmental dynamics : an official publication of the American Association of Anatomists · 2009
    Article
  14. Article
  15. Article
  16. Hierarchical approaches for systems modeling in cardiac development.Wiley interdisciplinary reviews. Systems biology and medicine
    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

2 authors at 1 institution in 1 country.

Shaheen AhmedDepartment of Oral Biology, College of Dentistry, University of Nebraska Medical Center, Lincoln, Nebr. 68583, USA.
Ali Nawshad
University of Nebraska Medical Center · US

Funding

SUPPRESSIVE ROLE OF TGFBETA IN METASTASIS OF COLON CANCERP20RR018759 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JOHNSON, KEITH R · 2003 to 2011
$17.9M
TGFbeta3 SIGNALING IN DEVELOPMENT OF PALATER01DE017986 · NIDCR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI NAWSHAD, ALI · 2008 to 2012
$1.8M
NCRR NIH HHS P20 RR018759NCRR NIH HHS RR018759NIDCR NIH HHS R01 DE017986
6 · The paper itself

Abstract

Epithelial-mesenchymal transition (EMT) is a highly conserved and fundamental process that governs morphogenesis in development and may also contribute to cancer metastasis. Transforming growth factor (TGF-beta) is a potent inducer of EMT in various developmental and tumor systems. The analysis of TGF-beta signal transduction pathways is now considered a critically important area of biology, since many defects occur in these pathways in embryonic development. The complexity of TGF-beta signal transduction networks is overwhelming due to the large numbers of interacting constituents, complicated feedforward, feedback and crosstalk circuitry mechanisms that they involve in addition to the cellular kinetics and enzymatics that contribute to cell signaling. As a result of this complexity, apparently simple but highly important questions remain unanswered, that is, how do epithelial cells respond to such TGF-beta signals? System biology and cellular kinetics play a crucial role in cellular function; omissions of such a critical contributor may lead to inaccurate understanding of embryonic EMT. In this review, we identify and explain why certain conditions need to be considered for a true representation of TGF-beta signaling in vivo to better understand the controlled, yet delicate mechanism of embryonic EMT.

Indexed as

Embryo, NonmammalianSignal TransductionAnimalsEmbryo, MammalianEpithelial CellsMesodermModels, BiologicalTransforming Growth Factor betaTransforming Growth Factor beta

Identifiers

PMID17587819
PMCPMC2043381
OpenAlexW2044215253

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.