Evidence map›Paper›PMID 20237511›Full record

ArticleGene therapy2010

Indirect imaging of cardiac-specific transgene expression using a bidirectional two-step transcriptional amplification strategy.

I Y Chen, O Gheysens, S Ray, Q Wang, P Padmanabhan, R Paulmurugan, A M Loening, M Rodriguez-Porcel, J K Willmann, A Y Sheikh and 7 more

Abstract read
In one paragraph

Article in Gene therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
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  10. Review
  11. Optical imaging for stem cell differentiation to neuronal lineage.Nuclear medicine and molecular imaging · 2012
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Engineering and visualization of bacteria for targeting infarcted myocardium.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Article
  17. In vivo imaging of intraprostatic-specific gene transcription by PET.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2011
    Article
  18. Review
  19. 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

17 authors at 3 institutions in 1 country.

I Y ChenDepartments of Radiology and Bioengineering, Bio-X Program, Stanford University, Stanford, CA 94305-5427, USA.
O Gheysens
S Ray
Q Wang
P Padmanabhan
R Paulmurugan
A M Loening
M Rodriguez-Porcel
J K Willmann
A Y Sheikh
C H Nielsen
G Hoyt
C H Contag
R C Robbins
S Biswal
J C Wu
S S Gambhir
Stanford University · USMayo Clinic · USStanford Medicine · US

Funding

Small Animal ImagingP50CA114747 · NCI · STANFORD UNIVERSITY · PI CONTAG, CHRISTOPHER H · 2005 to 2014
$18.2M
Molecular Imaging of Targeted Cardiac Gene TherapyR01HL093172 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2009 to 2015
$2.7M
Integrated Strategies for Novel Treatment of Myocardial IschemiaR01HL095571 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2010 to 2014
$2.0M
Multimodality Imaging of Cell Mediated Gene TransferR01HL078632 · NHLBI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2004 to 2007
$1.6M
Role of Oxidative Stress in Stem Cell Differentiation and SurvivalR00HL088048 · NHLBI · MAYO CLINIC ROCHESTER · PI RODRIGUEZ-PORCEL, MARTIN · 2009 to 2011
$747k
Role of Oxidative Stress in Stem Cell Differentiation and SurvivalK99HL088048 · NHLBI · MAYO CLINIC ROCHESTER · PI RODRIGUEZ-PORCEL, MARTIN · 2007 to 2008
$175k
NCI NIH HHS P50 CA114747NCI NIH HHS P50CA114747NHLBI NIH HHS 5R01HL078632NHLBI NIH HHS HL093172NHLBI NIH HHS HL095571NHLBI NIH HHS K99-R00 HL88048NHLBI NIH HHS R00 HL088048NHLBI NIH HHS R01 HL078632NHLBI NIH HHS R01 HL093172NHLBI NIH HHS R01 HL095571
6 · The paper itself

Abstract

Transcriptional targeting for cardiac gene therapy is limited by the relatively weak activity of most cardiac-specific promoters. We have developed a bidirectional plasmid vector, which uses a two-step transcriptional amplification (TSTA) strategy to enhance the expression of two optical reporter genes, firefly luciferase (fluc) and Renilla luciferase (hrluc), driven by the cardiac troponin T (cTnT) promoter. The vector was characterized in vitro and in living mice using luminometry and bioluminescence imaging to assess its ability to mediate strong, correlated reporter gene expression in a cardiac cell line and the myocardium, while minimizing expression in non-cardiac cell lines and the liver. In vitro, the TSTA system significantly enhanced cTnT-mediated reporter gene expression with moderate preservation of cardiac specificity. After intramyocardial and hydrodynamic tail vein delivery of an hrluc-enhanced variant of the vector, long-term fluc expression was observed in the heart, but not in the liver. In both the cardiac cell line and the myocardium, fluc expression correlated well with hrluc expression. These results show the vector's ability to effectively amplify and couple transgene expression in a cardiac-specific manner. Further replacement of either reporter gene with a therapeutic gene should allow non-invasive imaging of targeted gene therapy in living subjects.

Indexed as

Gene AmplificationGene TargetingGenetic VectorsGene Transfer TechniquesPlasmidsPromoter Regions, GeneticTransgenesAnimalsCell LineFemaleGenes, ReporterLiverLuciferases, FireflyLuciferases, RenillaMiceMice, Inbred BALB CLuciferases, FireflyLuciferases, RenillaTroponin

Identifiers

PMID20237511
PMCPMC2900530
OpenAlexW1967167181

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.