Evidence map›Paper›PMID 31635418›Full record

ArticleViruses2019

Novel Antiviral Activities of Obatoclax, Emetine, Niclosamide, Brequinar, and Homoharringtonine.

Petter I Andersen, Klara Krpina, Aleksandr Ianevski, Nastassia Shtaida, Eunji Jo, Jaewon Yang, Sandra Koit, Tanel Tenson, Veijo Hukkanen, Marit W Anthonsen and 5 more

Abstract read
In one paragraph

Article in Viruses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
–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

61 citing papers in PubMed, 1 synthesis or guideline pooled it.

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1 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

15 authors.

Petter I AndersenDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway. petteria@stud.ntnu.no.
Klara KrpinaDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway. klarak@stud.ntnu.no.
Aleksandr IanevskiDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway. aleksandr.ianevski@ntnu.no.
Nastassia ShtaidaInstitute of Technology, University of Tartu, 50090 Tartu, Estonia. nastassia.shtaida@ut.ee.
Eunji JoApplied Molecular Virology Laboratory, Institut Pasteur Korea, Sampyung-dong 696, Bundang-gu, Seongnam-si, Gyeonggi-do, Korea. eunji.jo@ip-korea.org.
Jaewon YangApplied Molecular Virology Laboratory, Institut Pasteur Korea, Sampyung-dong 696, Bundang-gu, Seongnam-si, Gyeonggi-do, Korea. jaewon.yang@ip-korea.org.
Sandra KoitInstitute of Technology, University of Tartu, 50090 Tartu, Estonia. sandra.koit@ut.ee.
Tanel TensonInstitute of Technology, University of Tartu, 50090 Tartu, Estonia. tanel.tenson@ut.ee.
Veijo HukkanenInstitute of Biomedicine, University of Turku, 20520 Turku, Finland. veijo.hukkanen@utu.fi.
Marit W AnthonsenDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway. marit.w.anthonsen@ntnu.no.
Magnar BjorasDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway. magnar.bjoras@ntnu.no.
Magnus EvanderDepartment of Clinical Microbiology, Virology, Umeå University, 90185 Umeå, Sweden. magnus.evander@umu.se.
Marc P WindischApplied Molecular Virology Laboratory, Institut Pasteur Korea, Sampyung-dong 696, Bundang-gu, Seongnam-si, Gyeonggi-do, Korea. magnus.evander@umu.se.
Eva ZusinaiteInstitute of Technology, University of Tartu, 50090 Tartu, Estonia. eva.zusinaite@ut.ee.
Denis E KainovDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway. denis.kainov@ntnu.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses are the major causes of acute and chronic infectious diseases in the world. According to the World Health Organization, there is an urgent need for better control of viral diseases. Repurposing existing antiviral agents from one viral disease to another could play a pivotal role in this process. Here, we identified novel activities of obatoclax and emetine against herpes simplex virus type 2 (HSV-2), echovirus 1 (EV1), human metapneumovirus (HMPV) and Rift Valley fever virus (RVFV) in cell cultures. Moreover, we demonstrated novel activities of emetine against influenza A virus (FLUAV), niclosamide against HSV-2, brequinar against human immunodeficiency virus 1 (HIV-1), and homoharringtonine against EV1. Our findings may expand the spectrum of indications of these safe-in-man agents and reinforce the arsenal of available antiviral therapeutics pending the results of further in vitro and in vivo tests.

Indexed as

AnimalsAntiviral AgentsBiphenyl CompoundsCell Culture TechniquesChlorocebus aethiopsDogsEmetineEnterovirus B, HumanHerpesvirus 2, HumanHIV-1HomoharringtonineHumansIndolesMadin Darby Canine Kidney CellsNiclosamidePyrrolesAntiviral AgentsBiphenyl CompoundsbrequinarEmetineHomoharringtonineIndolesNiclosamideobatoclaxPyrrolesQuinaldinesantiviral agentbroad-spectrum antiviraldrug targetsystems biologyvirus

Identifiers

PMID31635418
PMCPMC6832696

What OpenQuestion holds

Textmetadata
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.