Evidence map›Paper›PMID 20628903›Full record

ArticleMolecular imaging and biology2011

Evaluation of two internalizing carcinoembryonic antigen reporter genes for molecular imaging.

Bhaswati Barat, Vania E Kenanova, Tove Olafsen, Anna M Wu

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Non-invasive Reporter Gene Imaging of Cell Therapies, including T Cells and Stem Cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Review
  5. How Non-invasiveFrontiers in physiology · 2020
    Review
  6. Review
  7. Review
  8. 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

4 authors at 1 institution in 1 country.

Bhaswati BaratCrump Institute for Molecular Imaging, Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, Box 951770, 570 Westwood Plaza, Los Angeles, CA, 90095-1770, USA.
Vania E KenanovaCrump Institute for Molecular Imaging, Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, Box 951770, 570 Westwood Plaza, Los Angeles, CA, 90095-1770, USA.
Tove OlafsenCrump Institute for Molecular Imaging, Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, Box 951770, 570 Westwood Plaza, Los Angeles, CA, 90095-1770, USA.
Anna M WuCrump Institute for Molecular Imaging, Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, Box 951770, 570 Westwood Plaza, Los Angeles, CA, 90095-1770, USA. awu@mednet.ucla.edu.
Institute for Molecular Medicine · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
RECOMBINANT ANTI-CEA ANTIBODIESP01CA043904 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI RAUBITSCHEK, ANDREW A. · 1988 to 2012
$30.2M
Transductionally Redirected /Transcriptionally RestricteP50CA086306 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HERSCHMAN, HARVEY R. · 2000 to 2014
$29.0M
NCI NIH HHS CA 016042NCI NIH HHS CA 043904NCI NIH HHS CA 086306NCI NIH HHS P01 CA043904NCI NIH HHS P30 CA016042NCI NIH HHS P50 CA086306
6 · The paper itself

Abstract

purposeThe objective of this article is to develop internalizing positron emission tomography (PET) reporter genes for tracking genetically modified T cells in vivo. PROCEDURES: The transmembrane and cytoplasmic domains of the human transferrin receptor (TfR) and CD5 were each fused to the carcinoembryonic (CEA) minigene N-A3 and expressed in Jurkat T cells. Internalization was evaluated by confocal microscopy or by intracellular uptake of ¹²⁵I-labeled anti-CEA scFv-Fc. Reporter gene-transfected Jurkat xenografts in mice were analyzed by immunohistochemistry (IHC) and imaged by PET using ¹²⁴I- or ⁶⁴Cu-scFv-Fc as tracers.

resultsSurface expression of TR(1-99)-NA3 was lower than that of NA3-CD5. Both reporter genes were internalized following binding of the anti-CEA antibody fragment. IHC of tumors showed strong staining of NA3-CD5, whereas TR(1-99)-NA3 stained weakly. Specific targeting of TR(1-99)-NA3 or NA3-CD5 was shown by PET in xenografted mice.

conclusionsThe in vivo imaging studies suggest a potential application of the internalizing form of CEA (N-A3) as a PET reporter gene.

Indexed as

EndocytosisAnimalsCarcinoembryonic AntigenFemaleFlow CytometryGenes, ReporterHumansImmunoglobulin FragmentsImmunohistochemistryJurkat CellsMiceMice, NudeMolecular ImagingPositron-Emission TomographyRecombinant ProteinsTransfectionCarcinoembryonic AntigenImmunoglobulin FragmentsRecombinant Proteins

Identifiers

PMID20628903
PMCPMC2992604
OpenAlexW2004645774

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.