Evidence map›Paper›PMID 19471250›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2009

Converting tumor-specific markers into reporters of oncolytic virus infection.

Ianko D Iankov, Matthew L Hillestad, Allan B Dietz, Stephen J Russell, Evanthia Galanis

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Live Attenuated Measles Virus Vaccine ExpressingMolecular therapy oncolytics · 2020
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Oncolytic measles virus strains as novel anticancer agents.Expert opinion on biological therapy · 2013
    Review
  12. Attenuated oncolytic measles virus strains as cancer therapeutics.Current pharmaceutical biotechnology · 2012
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

5 authors at 1 institution in 1 country.

Ianko D IankovDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Matthew L Hillestad
Allan B Dietz
Stephen J Russell
Evanthia Galanis
Mayo Clinic · US

Funding

Targeted MV-CEA as a Potent Antitumor Agent against GBMP50CA108961 · NCI · MAYO CLINIC ROCHESTER · PI O'NEILL, BRIAN PATRICK · 2004 to 2015
$22.5M
NCI NIH HHS P50 CA108961NCI NIH HHS P50CA108961
6 · The paper itself

Abstract

Preferential killing of transformed cells, while keeping normal cells and organs unharmed, is the main goal of cancer gene therapy. Genetically engineered trackable markers and imaging reporters enable noninvasive monitoring of transduction efficiency and pharmacokinetics of anticancer virotherapeutics. However, none of these reporters can differentiate between infection in the targeted tumors and that in the normal tissue. Thus, we constructed oncolytic measles virus (MV) armed with a human light immunoglobulin chain reporter gene for the treatment of multiple myeloma (MM). Excessive production of monoclonal immunoglobulin is a key characteristic and marker for diagnostics of MM. Once expressed in infected target cells, vector-encoded lambda protein recombines with myeloma IgG-kappa immunoglobulin creating a unique IgG-kappa/lambda. A modified immunoassay technique allows precise quantification of converted marker molecules. Only antibody producing cells were able to assemble this chimeric immunoglobulin molecule, whereas other cells secreted only free lambda light chain. Human myeloma xenografts inoculated with lambda chain expressing MV secreted converted IgG-kappa/lambda in the plasma of tumor bearing animals and elevated reporter levels correlated with response to the therapy. This is the first report of a gene therapy vector engineered to discriminate between infection in malignant and normal cells by molecular modification of a tumor-specific protein.

Indexed as

AnimalsBiomarkers, TumorCell LineChlorocebus aethiopsElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayHumansImmunoblottingImmunoglobulin Light ChainsImmunohistochemistryMeasles virusMiceMice, SCIDMultiple MyelomaOncolytic VirotherapyOncolytic VirusesBiomarkers, TumorImmunoglobulin Light Chains

Identifiers

PMID19471250
PMCPMC2835235
OpenAlexW2080149678

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.