Evidence map›Paper›PMID 18941512›Full record

ArticlePloS one2008

Transcriptional and functional profiling of human embryonic stem cell-derived cardiomyocytes.

Feng Cao, Roger A Wagner, Kitchener D Wilson, Xiaoyan Xie, Ji-Dong Fu, Micha Drukker, Andrew Lee, Ronald A Li, Sanjiv S Gambhir, Irving L Weissman and 2 more

Abstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers.

0numbers the graph read from it
0cells of the map it votes in
135citing 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

135 citing papers in PubMed.

  1. Article
  2. Actin isoform-specific interactions revealed byProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Maturing heart muscle cells: Mechanisms and transcriptomic insights.Seminars in cell & developmental biology · 2021
    Review
  12. Article
  13. Proteomic analysis of mitochondrial biogenesis in cardiomyocytes differentiated from human induced pluripotent stem cells.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Human Cell Modeling for Cardiovascular Diseases.International journal of molecular sciences · 2020
    Review
  19. Review
  20. Review

75 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

12 authors.

Feng CaoDepartment of Radiology, Stanford University School of Medicine, Stanford, California, United States of America.
Roger A Wagner
Kitchener D Wilson
Xiaoyan Xie
Ji-Dong Fu
Micha Drukker
Andrew Lee
Ronald A Li
Sanjiv S Gambhir
Irving L Weissman
Robert C Robbins
Joseph C Wu

Funding

Small Animal ImagingP50CA114747 · NCI · STANFORD UNIVERSITY · PI PAIK, DAVID SEUNGWON · 2005 to 2014
$18.2M
Molecular Physiology of the Pacemaker ChannelsR01HL072857 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LI, RONALD A · 2004 to 2013
$3.4M
Nanostructuring and Molecular Imaging of Engineered Cardiovascular TissuesR33HL089027 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2009 to 2011
$2.3M
Nanostructuring and Molecular Imaging of Engineered Cardiovascular TissuesR21HL089027 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2007 to 2008
$777k
The Role of Novel Lim-Domain Proteins in CardiomyopathyK08HL076445 · NHLBI · STANFORD UNIVERSITY · PI WAGNER, ROGER A · 2004 to 2008
$655k
NCI NIH HHS CA114747NCI NIH HHS P50 CA114747NHLBI NIH HHS HL076445NHLBI NIH HHS HL089027NHLBI NIH HHS HL72857NHLBI NIH HHS K08 HL076445NHLBI NIH HHS R01 HL072857NHLBI NIH HHS R21 HL089027NHLBI NIH HHS R33 HL089027
6 · The paper itself

Abstract

Human embryonic stem cells (hESCs) can serve as a potentially limitless source of cells that may enable regeneration of diseased tissue and organs. Here we investigate the use of human embryonic stem cell-derived cardiomyocytes (hESC-CMs) in promoting recovery from cardiac ischemia reperfusion injury in a mouse model. Using microarrays, we have described the hESC-CM transcriptome within the spectrum of changes that occur between undifferentiated hESCs and fetal heart cells. The hESC-CMs expressed cardiomyocyte genes at levels similar to those found in 20-week fetal heart cells, making this population a good source of potential replacement cells in vivo. Echocardiographic studies showed significant improvement in heart function by 8 weeks after transplantation. Finally, we demonstrate long-term engraftment of hESC-CMs by using molecular imaging to track cellular localization, survival, and proliferation in vivo. Taken together, global gene expression profiling of hESC differentiation enables a systems-based analysis of the biological processes, networks, and genes that drive hESC fate decisions, and studies such as this will serve as the foundation for future clinical applications of stem cell therapies.

Indexed as

Gene Expression ProfilingAnimalsCell DifferentiationElectrocardiographyEmbryonic Stem CellsGraft SurvivalHumansMiceModels, AnimalMyocardial Reperfusion InjuryMyocytes, CardiacOligonucleotide Array Sequence AnalysisStem Cell TransplantationTranscription, GeneticTransplantation, HeterologousTreatment Outcome

Identifiers

PMID18941512
PMCPMC2565131

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.