Evidence map›Paper›PMID 21151140›Full record

ArticleNature medicine2011

Tumor-specific imaging through progression elevated gene-3 promoter-driven gene expression.

Hyo-eun C Bhang, Kathleen L Gabrielson, John Laterra, Paul B Fisher, Martin G Pomper

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

57 citing papers in PubMed, 88 citations in OpenAlex.

  1. Review
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  14. Molecular Imaging with Reporter Genes: Has Its Promise Been Delivered?Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
    Review
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  19. [Theranostics of osteosarcoma and lung metastasis with new integrin αZhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2019
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Hyo-eun C BhangDepartment of Pharmacology and Molecular Sciences, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
Kathleen L Gabrielson
John Laterra
Paul B Fisher
Martin G Pomper
Johns Hopkins University · USVirginia Commonwealth University · US

Funding

Translational Applications of mda-7/IL-24 in CancerP01CA104177 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2005 to 2009
$6.5M
MDA-7: Novel Cancer Therapeutic GeneR01CA097318 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2002 to 2012
$2.8M
Small Animal Imaging Resource (SAIR)U24CA092871 · NCI · JOHNS HOPKINS UNIVERSITY · PI POMPER, MARTIN G · 2007 to 2011
$2.3M
Pancreatic Cancer Management by Novel Gene Therapy & Dietary AgentsR01CA127641 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2009 to 2012
$1.2M
Screening strategy for small molecules inhibitors of cancerR03MH093195 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2011 to 2012
$75k
NCI NIH HHS P01 CA104177NCI NIH HHS R01 CA097318NCI NIH HHS R01 CA127641NCI NIH HHS U24 CA092871NCI NIH HHS U24 CA92871NIMH NIH HHS R03 MH093195
6 · The paper itself

Abstract

Molecular-genetic imaging is advancing from a valuable preclinical tool to a guide for patient management. The strategy involves pairing an imaging reporter gene with a complementary imaging agent in a system that can be used to measure gene expression or protein interaction or track gene-tagged cells in vivo. Tissue-specific promoters can be used to delineate gene expression in certain tissues, particularly when coupled with an appropriate amplification mechanism. Here we show that the progression elevated gene-3 (PEG-3) promoter, derived from a rodent gene mediating tumor progression and metastatic phenotypes, can be used to drive imaging reporters selectively to enable detection of micrometastatic disease in mouse models of human melanoma and breast cancer using bioluminescence and radionuclide-based molecular imaging techniques. Because of its strong promoter activity, tumor specificity and capacity for clinical translation, PEG-3 promoter-driven gene expression may represent a practical, new system for facilitating cancer imaging and therapy.

Indexed as

AnimalsDisease Models, AnimalGene Expression RegulationGenes, ReporterHumansLuciferasesMelanomaMiceMolecular BiologyMolecular ImagingNeoplasm MetastasisNeoplasmsPromoter Regions, GeneticProto-Oncogene ProteinsLuciferasesProto-Oncogene Proteins

Identifiers

PMID21151140
PMCPMC3057477
OpenAlexW2156054486

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.