Evidence map›Paper›PMID 17080479›Full record

ArticleProteomics2006

Proteomic analysis of reporter genes for molecular imaging of transplanted embryonic stem cells.

Joseph C Wu, Feng Cao, Sucharita Dutta, Xiaoyan Xie, Elmer Kim, Neil Chungfat, Sanjiv Gambhir, Sean Mathewson, Andrew J Connolly, Matthew Brown and 1 more

Abstract read
In one paragraph

Article in Proteomics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. In vivo imaging of embryonic stem cell therapy.European journal of nuclear medicine and molecular imaging · 2011
    Review
  12. Review
  13. Imaging of embryonic stem cell migration in vivo.Methods in molecular biology (Clifton, N.J.) · 2011
    Article
  14. Review
  15. Methods to assess stem cell lineage, fate and function.Advanced drug delivery reviews · 2010
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

11 authors at 1 institution in 1 country.

Joseph C WuDepartment of Radiology and Molecular Imaging Program at Stanford, Stanford University School of Medicine, Stanford, CA 94305, USA. joewu@stanford.edu
Feng Cao
Sucharita Dutta
Xiaoyan Xie
Elmer Kim
Neil Chungfat
Sanjiv Gambhir
Sean Mathewson
Andrew J Connolly
Matthew Brown
Evelyn W Wang
Stanford University · US

Funding

Small Animal ImagingP50CA114747 · NCI · STANFORD UNIVERSITY · PI MATIN, AC · 2005 to 2014
$18.2M
Multimodality Imaging of Cell Mediated Gene TransferR01HL078632 · NHLBI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2004 to 2007
$1.6M
Molecular Imaging of Cardiac Cell TransplantationK08HL074883 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2005 to 2008
$531k
NCI NIH HHS P50 CA114747NHLBI NIH HHS K08 HL074883NHLBI NIH HHS R01 HL078632
6 · The paper itself

Abstract

Study of stem cells may reveal promising treatment for diseases. The fate and function of transplanted stem cells remain poorly defined. Recent studies demonstrate that reporter genes can monitor real-time survival of transplanted stem cells in living subjects. We examined the effects of a novel and versatile triple fusion (TF) reporter gene construction on embryonic stem (ES) cell function by proteomic analysis. Murine ES cells were stably transduced with a self-inactivating lentiviral vector containing fluorescence (firefly luciferase; Fluc), bioluminescence (monomeric red fluorescence protein; mRFP), and positron emission tomography (herpes simplex virus type 1 truncated thymidine kinase; tTK) reporter genes. Fluorescence-activated cell sorting (FACS) analysis isolated stably transduced populations. TF reporter gene effects on cellular function were evaluated by quantitative proteomic profiling of control ES cells versus ES cells stably expressing the TF construct (ES-TF). Overall, no significant changes in protein quantity were observed. TF reporter gene expression had no effect on ES cell viability, proliferation, and differentiation capability. Molecular imaging studies tracked ES-TF cell survival and proliferation in living animals. In summary, this is the first proteomic study, demonstrating the unique potential of reporter gene imaging for tracking ES cell transplantation non-invasively, repetitively, and quantitatively.

Indexed as

ProteomicsAnimalsArtificial Gene FusionEmbryonic Stem CellsGene Expression ProfilingGenes, ReporterLentivirusLuminescent MeasurementsLuminescent ProteinsMiceOxygen IsotopesTransfectionLuminescent ProteinsOxygen Isotopes

Identifiers

PMID17080479
PMCPMC3683542
OpenAlexW2039307824

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.