Evidence map›Paper›PMID 22790962›Full record

ArticleCancer gene therapy2012

Preclinical efficacy of the oncolytic measles virus expressing the sodium iodide symporter in iodine non-avid anaplastic thyroid cancer: a novel therapeutic agent allowing noninvasive imaging and radioiodine therapy.

H V Reddi, P Madde, S J McDonough, M A Trujillo, J C Morris, R M Myers, K W Peng, S J Russell, B McIver, N L Eberhardt

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.9field-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

23 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Viral Vector-Based Cancer Vaccines.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  3. Article
  4. OncolyticTurkish journal of haematology : official journal of Turkish Society of Haematology · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Gene Therapy Today and Tomorrow.Diseases (Basel, Switzerland) · 2019
    Article
  10. Article
  11. Viral Vectors in Gene Therapy.Diseases (Basel, Switzerland) · 2018
    Review
  12. Potential and clinical translation of oncolytic measles viruses.Expert opinion on biological therapy · 2017
    Review
  13. Oncolytic viruses-immunotherapeutics on the rise.Journal of molecular medicine (Berlin, Germany) · 2016
    Review
  14. The current status of oncolytic viral therapy for head and neck cancer.World journal of otorhinolaryngology - head and neck surgery · 2016
    Review
  15. Review
  16. Article
  17. PET imaging of oncolytic VSV expressing the mutant HSV-1 thymidine kinase transgene in a preclinical HCC rat model.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
    Article
  18. Review
  19. Article
  20. Progress in oncolytic virotherapy for the treatment of thyroid malignant neoplasm.Journal of experimental & clinical cancer research : CR · 2014
    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

10 authors at 1 institution in 1 country.

H V ReddiDivision of Endocrinology, Department of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA.
P Madde
S J McDonough
M A Trujillo
J C Morris
R M Myers
K W Peng
S J Russell
B McIver
N L Eberhardt
Mayo Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anaplastic thyroid cancer is an extremely aggressive disease resistant to radioiodine treatment because of loss of sodium iodide symporter (NIS) expression. To enhance prognosis of this fatal cancer, we validated the preclinical efficacy of measles virus (MV)-NIS, the vaccine strain of the oncolytic MV (MV-Edm), modified to include the NIS gene. Western blotting analysis confirmed that a panel of eight anaplastic thyroid cancer (ATC)-derived cell lines do not express NIS protein, but do express CD46, the MV receptor. In vitro cell death assays and in vivo xenograft studies demonstrate the oncolytic efficacy of MV-NIS in BHT-101 and KTC-3, ATC-derived cell lines. Radioactive iodine uptake along with single-photon emission computed tomography (SPECT)-computed tomography imaging of KTC-3 xenografts after (99)Tc(m) administration confirmed NIS expression in vitro and in vivo, respectively, after virus treatment. Adjuvant administration of RAI, to MV-NIS-treated KTC-3 tumors showed a trend for increased tumor cell killing. As current treatment for ATC is only palliative, and MV-NIS is currently Food and Drug Administration approved for human clinical trials in myeloma, our data indicate that targeting ATC with MV-NIS could prove to be a novel therapeutic strategy for effective treatment of iodine-resistant ATC and will expedite its testing in clinical trials for this aggressive disease.

Indexed as

AnimalsBlotting, WesternCell Line, TumorChlorocebus aethiopsFemaleGenetic TherapyHumansIodineIodine RadioisotopesMeasles virusMembrane Cofactor ProteinMiceMice, NudeOncolytic VirotherapyOncolytic VirusesReceptors, VirusCD46 protein, humanIodineIodine RadioisotopesMembrane Cofactor ProteinReceptors, VirusSodium-Iodide SymportersSymporters

Identifiers

PMID22790962
OpenAlexW1996985452

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.