Evidence map›Paper›PMID 22402364›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2012

c-Myc is required for proper coronary vascular formation via cell- and gene-specific signaling.

Colby A Souders, Stephanie L K Bowers, Indroneal Banerjee, John W Fuseler, Jennifer L Demieville, Troy A Baudino

Open access · greenAbstract readComparative Study
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 33% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy.The Journal of clinical investigation · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Linking tumor-associated macrophages, inflammation, and intestinal tumorigenesis: role of MCP-1.American journal of physiology. Gastrointestinal and liver physiology · 2012
    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

6 authors at 2 institutions in 1 country.

Colby A SoudersDepartment of Medicine, Division of Molecular Cardiology, Cardiovascular Research Institute, Texas A&M Health Science Center, Temple, TX 76504, USA.
Stephanie L K Bowers
Indroneal Banerjee
John W Fuseler
Jennifer L Demieville
Troy A Baudino
University of South Carolina · USUniversity of California, San Diego · US

Funding

Dynamic Interaction Between Cardiac Fibroblasts, Myocytes and the ECMR01HL085847 · NHLBI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI BORG, THOMAS K · 2008 to 2012
$1.8M
NHLBI NIH HHS HL-85847NHLBI NIH HHS R01 HL085847
6 · The paper itself

Abstract

objectiveAlthough significant research has detailed angiogenesis during development and cancer, little is known about cardiac angiogenesis, yet it is critical for survival following pathological insult. The transcription factor c-Myc is a target of anticancer therapies because of its mitogenic and proangiogenic induction. In the current study, we investigate its role in cardiac angiogenesis in a cell-dependent and gene-specific context. METHODS AND

resultsAngiogenesis assays using c-Myc-deficient cardiac endothelial cells and fibroblasts demonstrate that c-Myc is essential to vessel formation, and fibroblast-mediated vessel formation is dependent on c-Myc expression in fibroblasts. Gene analyses revealed that c-Myc-mediated gene expression is unique in cardiac angiogenesis and varies in a cell-dependent manner. In vitro 3-dimensional cultures demonstrated c-Myc's role in the expression of secreted angiogenic factors, while also providing evidence for c-Myc-mediated cell-cell interactions. Additional in vivo vascular analyses support c-Myc's critical role in capillary formation and vessel patterning during development and also in response to a pathological stimulus where its expression in myocytes is required for angiogenic remodeling.

conclusionsThese data demonstrate that proper c-Myc expression in cardiac fibroblasts and myocytes is essential to cardiac angiogenesis. These results have the potential for novel therapeutic applications involving the angiogenic response during cardiac remodeling.

Indexed as

Signal TransductionAnimalsCell CommunicationCells, CulturedCoronary VesselsMaleMiceMice, Inbred C57BLMicroscopy, ConfocalNeovascularization, PhysiologicPolymerase Chain ReactionProto-Oncogene Proteins c-mycRNAProto-Oncogene Proteins c-mycRNA

Identifiers

PMID22402364
PMCPMC3363000
OpenAlexW1973758802

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.