Evidence map›Paper›PMID 27738655›Full record

ArticleMolecular therapy oncolytics2016

Application of interferon modulators to overcome partial resistance of human ovarian cancers to VSV-GP oncolytic viral therapy.

Catherine Dold, Carles Rodriguez Urbiola, Guido Wollmann, Lisa Egerer, Alexander Muik, Lydia Bellmann, Heidelinde Fiegl, Christian Marth, Janine Kimpel, Dorothee von Laer

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
8.1field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
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  6. Review
  7. Article
  8. Characterization of VSV-GP morphology by cryo-EM imaging and SEC-MALS.Molecular therapy. Methods & clinical development · 2025
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Repeated harvest enables efficient production of VSV-GP.Frontiers in bioengineering and biotechnology · 2024
    Article
  19. Oncolytic virus and inhibitor for NEDD8-activating enzyme pevonedistat: Promising combination for cancer therapy?Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  20. A comprehensive study of SARS-CoV-2 main protease (MbioRxiv : the preprint server for biology · 2023
    Article

4 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Catherine DoldDivision of Virology, Medical University of Innsbruck , Innsbruck, Austria.
Carles Rodriguez UrbiolaDivision of Virology, Medical University of Innsbruck , Innsbruck, Austria.
Guido WollmannDivision of Virology, Medical University of Innsbruck , Innsbruck, Austria.
Lisa EgererDivision of Virology, Medical University of Innsbruck , Innsbruck, Austria.
Alexander MuikApplied Virology and Gene Therapy Unit , Frankfurt am Main, Germany.
Lydia BellmannDivision of Virology, Medical University of Innsbruck , Innsbruck, Austria.
Heidelinde FieglDepartment of Gynecology and Obstetrics, Medical University of Innsbruck , Innsbruck, Austria.
Christian MarthDepartment of Gynecology and Obstetrics, Medical University of Innsbruck , Innsbruck, Austria.
Janine KimpelDivision of Virology, Medical University of Innsbruck , Innsbruck, Austria.
Dorothee von LaerDivision of Virology, Medical University of Innsbruck , Innsbruck, Austria.
Universität Innsbruck · ATInnsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously, we described an oncolytic vesicular stomatitis virus variant pseudotyped with the nonneurotropic glycoprotein of the lymphocytic choriomeningitis virus, VSV-GP, which was highly effective in glioblastoma. Here, we tested its potency for the treatment of ovarian cancer, a leading cause of death from gynecological malignancies. Effective oncolytic activity of VSV-GP could be demonstrated in ovarian cancer cell lines and xenografts in mice; however, remission was temporary in most mice. Analysis of the innate immune response revealed that ovarian cancer cell lines were able to respond to and produce type I interferon, inducing an antiviral state upon virus infection. This is in stark contrast to published data for other cancer cell lines, which were mostly found to be interferon incompetent. We showed that

Identifiers

PMID27738655
PMCPMC5040171
OpenAlexW2525631210

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.