Evidence map›Paper›PMID 22096252›Full record

ArticleBlood2012

The adaptor protein Shc integrates growth factor and ECM signaling during postnatal angiogenesis.

Daniel Timothy Sweet, Zhongming Chen, David M Wiley, Victoria L Bautch, Ellie Tzima

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Endothelial Mechanosignaling: Does One Sensor Fit All?Antioxidants & redox signaling · 2016
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
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  18. 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

5 authors at 3 institutions in 3 countries.

Daniel Timothy SweetCurriculum in Genetics & Molecular Biology, University of North Carolina, Chapel Hill, NC, USA.
Zhongming Chen
David M Wiley
Victoria L Bautch
Ellie Tzima
Institut thématique Génétique, génomique et bioinformatique · FRInstitute of Molecular and Cell Biology · RUUniversity of North Carolina at Chapel Hill · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Pre-doctoral Training Program in Integrative Vascular BiologyT32HL069768 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Christopher P. Mack · 2002 to 2026
$9.7M
NRSA IN GENETICST32GM007092 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEKELSKY, JEFF J. · 1985 to 2019
$5.9M
MOLECULAR CONTROL OF ANGIOGENESISR01HL043174 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BAUTCH, VICTORIA L · 1989 to 2017
$4.7M
Endothelial cell junctions in mechanotransductionR01HL088632 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TZIMA, ELLIE · 2008 to 2012
$2.1M
NCI NIH HHS P30 CA016086NHLBI NIH HHS HL088632NHLBI NIH HHS R01 HL043174NHLBI NIH HHS R01 HL088632NHLBI NIH HHS R01 HL43174NHLBI NIH HHS T32 HL069768NIGMS NIH HHS T32 GM007092
6 · The paper itself

Abstract

Angiogenesis requires integration of cues from growth factors, extracellular matrix (ECM) proteins, and their receptors in endothelial cells. In the present study, we show that the adaptor protein Shc is required for angiogenesis in zebrafish, mice, and cell-culture models. Shc knockdown zebrafish embryos show defects in intersegmental vessel sprouting in the trunk. Shc flox/flox; Tie2-Cre mice display reduced angiogenesis in the retinal neovascularization model and in response to VEGF in the Matrigel plug assay in vivo. Functional studies reveal a model in which Shc is required for integrin-mediated spreading and migration specifically on fibronectin, as well as endothelial cell survival in response to VEGF. Mechanistically, Shc is required for activation of the Akt pathway downstream of both integrin and VEGF signaling, as well as for integration of signals from these 2 receptors when cells are grown on fibronectin. Therefore, we have identified a unique mechanism in which signals from 2 critical angiogenic signaling axes, integrins and VEGFR-2, converge at Shc to regulate postnatal angiogenesis.

Indexed as

Signal TransductionAnimalsApoptosisBlotting, WesternCell MovementCells, CulturedEmbryo, NonmammalianExtracellular MatrixFemaleFibronectinsGene Knockdown TechniquesHumansHuman Umbilical Vein Endothelial CellsIntegrinsIntercellular Signaling Peptides and ProteinsMaleFibronectinsIntegrinsIntercellular Signaling Peptides and ProteinsProto-Oncogene Proteins c-aktShc Signaling Adaptor ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Zebrafish Proteins

Identifiers

PMID22096252
PMCPMC3293649
OpenAlexW2053559839

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.