Evidence map›Paper›PMID 25132472›Full record

ReviewMicrovascular research2014

Lymphatic fate specification: an ERK-controlled transcriptional program.

Pengchun Yu, Joe K Tung, Michael Simons

Abstract readReview
In one paragraph

Review in Microvascular research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Cardiac lymphatics in health and disease.Nature reviews. Cardiology · 2019
    Review
  10. Endothelial Metabolic Control of Lymphangiogenesis.BioEssays : news and reviews in molecular, cellular and developmental biology · 2018
    Review
  11. Article
  12. Metabolic Analysis of Lymphatic Endothelial Cells.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  13. Article
  14. 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

3 authors.

Pengchun YuYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, New Haven, CT 06520, United States.
Joe K TungYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, New Haven, CT 06520, United States.
Michael SimonsYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, New Haven, CT 06520, United States; Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06520, United States. Electronic address: michael.simons@yale.edu.

Funding

Angiogensis and ischemiaR01HL053793 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 1996 to 2017
$7.3M
Arteriogenesis and BranchingR01HL084619 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 2007 to 2018
$6.7M
NHLBI NIH HHS HL084619NHLBI NIH HHS R01 HL053793NHLBI NIH HHS R01 HL084619
6 · The paper itself

Abstract

Lymphatic vessels are intimately involved in the regulation of water and solute homeostasis by returning interstitial fluid back to the venous circulation and play an equally important role in immune responses by providing avenues for immune cell transport. Defects in the lymphatic vasculature result in a number of pathological conditions, including lymphedema and lymphangiectasia. Knowledge of molecular mechanisms underlying lymphatic development and maintenance is therefore critical for understanding, prevention and treatment of lymphatic circulation-related diseases. Research in the past two decades has uncovered several key transcriptional factors (Prox1, Sox18 and Coup-TFII) controlling lymphatic fate specification. Most recently, ERK signaling has emerged as a critical regulator of this transcriptional program. This review summarizes our current understanding of lymphatic fate determination and its transcriptional controls.

Indexed as

AnimalsCell LineageExtracellular Signal-Regulated MAP KinasesHomeodomain ProteinsHumansLymphangiogenesisLymphatic VesselsMiceModels, BiologicalProspero-Related Homeobox 1 ProteinReceptors, NotchSignal TransductionSOXF Transcription FactorsTranscription, GeneticTumor Suppressor ProteinsVascular Endothelial Growth Factor AExtracellular Signal-Regulated MAP KinasesHomeodomain ProteinsProspero-Related Homeobox 1 ProteinReceptors, NotchSox18 protein, mouseSOXF Transcription FactorsTumor Suppressor ProteinsVascular Endothelial Growth Factor AERKLymphangiogenesisLymphatic fateProx1Sox18VEGF-C

Identifiers

PMID25132472
PMCPMC4268409

What OpenQuestion holds

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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.