Evidence map›Paper›PMID 31372363›Full record

ArticleOncolytic virotherapy2019

Directed evolution as a tool for the selection of oncolytic RNA viruses with desired phenotypes.

Sergei S Zainutdinov, Galina V Kochneva, Sergei V Netesov, Peter M Chumakov, Olga V Matveeva

Abstract read
In one paragraph

Article in Oncolytic virotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

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  10. Article
  11. Genetic Modifications That Expand Oncolytic Virus Potency.Frontiers in molecular biosciences · 2022
    Review
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  13. Review
  14. Article
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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.

Sergei S ZainutdinovState Research Center of Virology and Biotechnology "Vector" , Koltsovo 630559, Russia.
Galina V KochnevaState Research Center of Virology and Biotechnology "Vector" , Koltsovo 630559, Russia.
Sergei V NetesovDepartment of Natural Sciences, Novosibirsk State University, Novosibirsk 630090, Russia.
Peter M ChumakovEngelhardt Institute of Molecular Biology , Moscow 119991, Russia.
Olga V MatveevaSATOR Therapeutics LLC , Cleveland, OH 44106, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses have some characteristics in common with cell-based life. They can evolve and adapt to environmental conditions. Directed evolution can be used by researchers to produce viral strains with desirable phenotypes. Through bioselection, improved strains of oncolytic viruses can be obtained that have better safety profiles, increased specificity for malignant cells, and more efficient spread among tumor cells. It is also possible to select strains capable of killing a broader spectrum of cancer cell variants, so as to achieve a higher frequency of therapeutic responses. This review describes and analyses virus adaptation studies performed with members of four RNA virus families that are used for viral oncolysis: reoviruses, paramyxoviruses, enteroviruses, and rhabdoviruses.

Indexed as

directed viral evolutiononcolytic virusesvirus adaptationvirus selection

Identifiers

PMID31372363
PMCPMC6636189

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.