Evidence map›Paper›PMID 29795047›Full record

ArticleViruses2018

Saracatinib Inhibits Middle East Respiratory Syndrome-Coronavirus Replication In Vitro.

Jin Soo Shin, Eunhye Jung, Meehyein Kim, Ralph S Baric, Yun Young Go

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 2 pooled it
9.2field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 2 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Advancements in the development of antivirals against SARS-Coronavirus.Frontiers in cellular and infection microbiology · 2025
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  7. Prospects ofHeliyon · 2024
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  11. Article
  12. Kinase Inhibitors as Underexplored Antiviral Agents.Journal of medicinal chemistry · 2022
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Pathomechanisms, therapeutic targets and potent inhibitors of some beta-coronaviruses from bench-to-bedside.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2021
    Review
  19. Article
  20. Article
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 3 institutions in 2 countries.

Jin Soo ShinVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea. jsshin@krict.re.kr.
Eunhye JungVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea. e-hyeya@hanmail.net.ORCID 0000-0001-6329-9431
Meehyein KimVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea. mkim@krict.re.kr.
Ralph S BaricDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. rbaric@email.unc.edu.
Yun Young GoVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea. yygo@krict.re.kr.
Korea Research Institute of Chemical Technology · KRKorea Advanced Institute of Science and Technology · KRUniversity of North Carolina at Chapel Hill · US

Funding

Screening CoreU19AI109680 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NELSON, JAY A · 2014 to 2018
$34.9M
NIAID NIH HHS U19 AI109680
6 · The paper itself

Abstract

The Middle East respiratory syndrome-coronavirus (MERS-CoV), first identified in Saudi Arabia, is an emerging zoonotic pathogen that causes severe acute respiratory illness in humans with a high fatality rate. Since its emergence, MERS-CoV continues to spread to countries outside of the Arabian Peninsula and gives rise to sporadic human infections following the entry of infected individuals to other countries, which can precipitate outbreaks similar to the one that occurred in South Korea in 2015. Current therapeutics against MERS-CoV infection have primarily been adapted from previous drugs used for the treatment of severe acute respiratory syndrome. In search of new potential drug candidates, we screened a library composed of 2334 clinically approved drugs and pharmacologically active compounds. The drug saracatinib, a potent inhibitor of Src-family of tyrosine kinases (SFK), was identified as an inhibitor of MERS-CoV replication in vitro. Our results suggest that saracatinib potently inhibits MERS-CoV at the early stages of the viral life cycle in Huh-7 cells, possibly through the suppression of SFK signaling pathways. Furthermore, saracatinib exhibited a synergistic effect with gemcitabine, an anticancer drug with antiviral activity against several RNA viruses. These data indicate that saracatinib alone or in combination with gemcitabine can provide a new therapeutic option for the treatment of MERS-CoV infection.

Indexed as

Antiviral AgentsBenzodioxolesCell LineCross InfectionDeoxycytidineDNA ReplicationDrug DiscoveryEnzyme InhibitorsGemcitabineHumansMiddle East Respiratory Syndrome CoronavirusQuinazolinesSmall Molecule Librariessrc-Family KinasesVirus ReplicationAntiviral AgentsBenzodioxolesDeoxycytidineEnzyme InhibitorsGemcitabineQuinazolinessaracatinibSmall Molecule Librariessrc-Family KinasesgemcitabineMERS-CoVMiddle East Respiratory SyndromesaracatinibSrc-family kinase inhibitor

Identifiers

PMID29795047
PMCPMC6024778
OpenAlexW2804307646

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.