Evidence map›Paper›PMID 25358248›Full record

ArticleOncotarget2014

Apoptin enhances the oncolytic properties of vaccinia virus and modifies mechanisms of tumor regression.

Galina Kochneva, Evgeniy Zonov, Antonina Grazhdantseva, Anastasiya Yunusova, Galina Sibolobova, Evgeniy Popov, Oleg Taranov, Sergei Netesov, Peter Chumakov, Elena Ryabchikova

Abstract read
In one paragraph

Article in Oncotarget, 2014. 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.

  1. Article
  2. Review
  3. Article
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  5. Review
  6. Article
  7. Bivalent EGFR-Targeting DARPin-MMAE Conjugates.International journal of molecular sciences · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Prospects for combined use of oncolytic viruses and CAR T-cells.Journal for immunotherapy of cancer · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
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  20. 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.

Galina KochnevaNovosibirsk State University, Novosibirsk, Russia. State Research Center of Virology and Biotechnology "Vector", Koltsovo, Russia.
Evgeniy ZonovInstitute of Chemical Biology and Fundamental Medicine, SB RAS, Novosibirsk, Russia.
Antonina GrazhdantsevaState Research Center of Virology and Biotechnology "Vector", Koltsovo, Russia.
Anastasiya YunusovaNovosibirsk State University, Novosibirsk, Russia. Institute of Chemical Biology and Fundamental Medicine, SB RAS, Novosibirsk, Russia.
Galina SibolobovaState Research Center of Virology and Biotechnology "Vector", Koltsovo, Russia.
Evgeniy PopovNovosibirsk State University, Novosibirsk, Russia. State Research Center of Virology and Biotechnology "Vector", Koltsovo, Russia.
Oleg TaranovState Research Center of Virology and Biotechnology "Vector", Koltsovo, Russia.
Sergei NetesovNovosibirsk State University, Novosibirsk, Russia. State Research Center of Virology and Biotechnology "Vector", Koltsovo, Russia.
Peter ChumakovNovosibirsk State University, Novosibirsk, Russia. Engelhardt Institute of Molecular Biology, Moscow.
Elena RyabchikovaNovosibirsk State University, Novosibirsk, Russia. Institute of Chemical Biology and Fundamental Medicine, SB RAS, Novosibirsk, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recombinant vaccinia virus VVdGF-ApoS24/2 expressing apoptin selectively kills human cancer cells in vitro [Kochneva et al., 2013]. We compared the oncolytic activity of this recombinant with that of the parental strain L-IVP using a model of human A431 carcinoma xenografts in nude mice. Single intratumoral injections (2×10^7 PFU/mouse) of the viruses produced a dramatic decrease in tumor volumes, which was higher after injection of apoptin-producing virus. The tumor dried out after the injection of recombinant while injection of L-IVP strain resulted in formation of cavities filled with cell debris and liquid. Both viruses rapidly spread in xenografts and replicate exclusively in tumor cells causing their destruction within 8 days. Both viruses induced insignificant level of apoptosis in tumors. Unlike the previously described nuclear localization of apoptin in cancer cells the apoptin produced by recombinant virus was localized to the cytoplasm. The apoptin did not induce a typical apoptosis, but it rather influenced pathway of cell death and thereby caused tumor shrinkage. The replacement of destroyed cells by filamentous material is the main feature of tumor regression caused by the VVdGF-ApoS24/2 virus. The study points the presence of complicated mechanisms of apoptin effects at the background of vaccinia virus replication.

Indexed as

AnimalsApoptosisCarcinoma, Squamous CellCell Line, TumorFemaleHaplorhiniHumansMiceMice, NudeOncolytic VirotherapyVaccinia virusVirus ReplicationXenograft Model Antitumor Assays

Identifiers

PMID25358248
PMCPMC4294355

What OpenQuestion holds

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LicenceCC BY
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.