Evidence map›Paper›PMID 35146614›Full record

ArticleMolecular imaging and biology2022

A Human-derived Dual MRI/PET Reporter Gene System with High Translational Potential for Cell Tracking.

Nourhan Shalaby, John Kelly, Francisco Martinez, Mathew Fox, Qi Qi, Jonathan Thiessen, Justin Hicks, Timothy J Scholl, John A Ronald

Open access · greenAbstract read
In one paragraph

Article in Molecular imaging and biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Visualizing cell-cell communication using synthetic notch activated MRI.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Reporter Genes for Brain Imaging Using MRI, SPECT and PET.International journal of molecular sciences · 2022
    Review
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

9 authors at 3 institutions in 2 countries.

Nourhan ShalabyDepartment of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada. nshalaby@uwo.ca.ORCID http://orcid.org/0000-0001-9264-7191
John KellyRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Francisco MartinezRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Mathew FoxLawson Health Research Institute, London, Canada.
Qi QiDepartment of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Jonathan ThiessenRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Justin HicksRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Timothy J SchollDepartment of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
John A RonaldDepartment of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Western University · CALawson Health Research Institute · CAOntario Institute for Cancer Research · CA

Funding

Non-Invasive Monitoring of CRISPR/Cas-Edited Chimeric Antigen Receptor T (CAR-T) Cells with Reporter Gene-Based Magnetic Resonance Imaging and Positron Emission TomographyUH3EB028907 · NIBIB · UNIVERSITY OF WESTERN ONTARIO · PI RONALD, JOHN ANDREW · 2021 to 2022
$648k
Non-Invasive Monitoring of CRISPR/Cas-Edited Chimeric Antigen Receptor T (CAR-T) Cells with Reporter Gene-Based Magnetic Resonance Imaging and Positron Emission TomographyUH2EB028907 · NIBIB · UNIVERSITY OF WESTERN ONTARIO · PI RONALD, JOHN ANDREW · 2019 to 2020
$323k
NIBIB NIH HHS UH2 EB028907NIBIB NIH HHS UH3 EB028907
6 · The paper itself

Abstract

purposeReporter gene imaging has been extensively used to longitudinally report on whole-body distribution and viability of transplanted engineered cells. Multi-modal cell tracking can provide complementary information on cell fate. Typical multi-modal reporter gene systems often combine clinical and preclinical modalities. A multi-modal reporter gene system for magnetic resonance imaging (MRI) and positron emission tomography (PET), two clinical modalities, would be advantageous by combining the sensitivity of PET with the high-resolution morphology and non-ionizing nature of MRI. PROCEDURES: We developed and evaluated a dual MRI/PET reporter gene system composed of two human-derived reporter genes that utilize clinical reporter probes for engineered cell detection. As a proof-of-concept, breast cancer cells were engineered to co-express the human organic anion transporter polypeptide 1B3 (OATP1B3) that uptakes the clinical MRI contrast agent gadolinium ethoxybenzyl-diethylenetriaminepentaacetic acid (Gd-EOB-DTPA), and the human sodium iodide symporter (NIS) which uptakes the PET tracer, [

resultsT

conclusionsOur study demonstrates the ability to noninvasively track cells engineered with our human-derived dual MRI/PET reporter system, enabling a more comprehensive evaluation of transplanted cells. Future work is focused on applying this tool to track therapeutic cells, which may one day enable the broader application of cell tracking within the healthcare system.

Indexed as

Cell TrackingGadolinium DTPAAnimalsContrast MediaGenes, ReporterHumansMagnetic Resonance ImagingMicePositron-Emission TomographyContrast MediaGadolinium DTPACell trackingContrast agentsMRIPETReporter genesReporter probes

Identifiers

PMID35146614
PMCPMC9235057
OpenAlexW4211162220

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.