Evidence map›Paper›PMID 17960161›Full record

ArticleGene therapy2007

SPECT/CT imaging of oncolytic adenovirus propagation in tumours in vivo using the Na/I symporter as a reporter gene.

A Merron, I Peerlinck, P Martin-Duque, J Burnet, M Quintanilla, S Mather, M Hingorani, K Harrington, R Iggo, G Vassaux

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Spatiotemporal PET Imaging Reveals Differences in CAR-T Tumor Retention in Triple-Negative Breast Cancer Models.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  5. 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
  6. How Non-invasiveFrontiers in physiology · 2020
    Review
  7. Review
  8. Experimental and therapeutic medicine · 2018
    Article
  9. Cousins at work: How combining medical with optical imaging enhances in vivo cell tracking.The international journal of biochemistry & cell biology · 2018
    Review
  10. Article
  11. Article
  12. [Scientific reports · 2017
    Article
  13. Article
  14. Review
  15. Article
  16. Perfusion Pressure Is a Critical Determinant of the Intratumoral Extravasation of Oncolytic Viruses.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Article
  17. Review
  18. Molecular imaging of oncolytic viral therapy.Molecular therapy oncolytics · 2015
    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

10 authors at 7 institutions in 3 countries.

A MerronCentre for Molecular Oncology, Institute of Cancer, Queen Mary's School of Medicine and Dentistry, London, UK.
I Peerlinck
P Martin-Duque
J Burnet
M Quintanilla
S Mather
M Hingorani
K Harrington
R Iggo
G Vassaux
Queen Mary University of London · GBInstitute of Cancer Research · GBCancer Research UK · GBIMT Atlantique · FRInstituto de Investigaciones Biomédicas Sols-Morreale · ESUniversidad Francisco de Vitoria · ESUniversity of St Andrews · GB

Funding

Medical Research Council G84/6703
6 · The paper itself

Abstract

Oncolytic adenoviruses have shown some promise in cancer gene therapy. However, their efficacy in clinical trials is often limited, and additional therapeutic interventions have been proposed to increase their efficacies. In this context, molecular imaging of viral spread in tumours could provide unique information to rationalize the timing of these combinations. Here, we use the human sodium iodide symporter (hNIS) as a reporter gene in wild-type and replication-selective adenoviruses. By design, hNIS cDNA is positioned in the E3 region in a wild-type adenovirus type 5 (AdIP1) and in an adenovirus in which a promoter from the human telomerase gene (RNA component) drives E1 expression (AdAM6). Viruses show functional hNIS expression and replication in vitro and kinetics of spread of the different viruses in tumour xenografts are visualized in vivo using a small animal nano-SPECT/CT camera. The time required to reach maximal spread is 48 h for AdIP1 and 72 h for AdAM6 suggesting that genetic engineering of adenoviruses can affect their kinetics of spread in tumours. Considering that this methodology is potentially clinically applicable, we conclude that hNIS-mediated imaging of viral spread in tumours may be an important tool for combined anticancer therapies involving replicating adenoviruses

Indexed as

Genes, ReporterTomography, Emission-Computed, Single-PhotonAdenoviridaeAdenoviridae InfectionsAnimalsColonic NeoplasmsGene ExpressionGenetic TherapyHumansInjections, IntralesionalMiceMice, Inbred BALB CNeoplasm TransplantationOncolytic VirotherapySodium-Iodide SymportersSymportersSodium-Iodide SymportersSymporters

Identifiers

PMID17960161
OpenAlexW2045242103

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.