Evidence map›Paper›PMID 32482672›Full record

ArticleAntimicrobial agents and chemotherapy2020

Identification of Estrogen Receptor Modulators as Inhibitors of Flavivirus Infection.

Nicholas S Eyre, Emily N Kirby, Daniel R Anfiteatro, Gustavo Bracho, Alice G Russo, Peter A White, Amanda L Aloia, Michael R Beard

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Nicholas S EyreResearch Centre for Infectious Diseases, School of Biological Sciences, University of Adelaide, Adelaide, Australia nicholas.eyre@adelaide.edu.au.ORCID 0000-0002-5424-7573
Emily N Kirby *Research Centre for Infectious Diseases, School of Biological Sciences, University of Adelaide, Adelaide, Australia.
Daniel R Anfiteatro *Research Centre for Infectious Diseases, School of Biological Sciences, University of Adelaide, Adelaide, Australia.
Gustavo Bracho *Cell Screen SA, Flinders Centre for Innovation in Cancer, Flinders University, Bedford Park, Australia.
Alice G RussoSchool of Biotechnology and Biomolecular Sciences, Faculty of Science, The University of New South Wales, Sydney, Australia.
Peter A WhiteSchool of Biotechnology and Biomolecular Sciences, Faculty of Science, The University of New South Wales, Sydney, Australia.ORCID 0000-0002-6046-9631
Amanda L Aloia *Cell Screen SA, Flinders Centre for Innovation in Cancer, Flinders University, Bedford Park, Australia.
Michael R Beard *Research Centre for Infectious Diseases, School of Biological Sciences, University of Adelaide, Adelaide, Australia.
South Australia Pathology · AUFlinders University · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flaviviruses such as Zika virus (ZIKV), dengue virus (DENV), and West Nile virus (WNV) are major global pathogens for which safe and effective antiviral therapies are not currently available. To identify antiviral small molecules with well-characterized safety and bioavailability profiles, we screened a library of 2,907 approved drugs and pharmacologically active compounds for inhibitors of ZIKV infection using a high-throughput cell-based immunofluorescence assay. Interestingly, estrogen receptor modulators raloxifene hydrochloride and quinestrol were among 15 compounds that significantly inhibited ZIKV infection in repeat screens. Subsequent validation studies revealed that these drugs effectively inhibit ZIKV, DENV, and WNV (Kunjin strain) infection at low micromolar concentrations with minimal cytotoxicity in Huh-7.5 hepatoma cells and HTR-8 placental trophoblast cells. Since these cells lack detectable expression of estrogen receptors-α and -β (ER-α and ER-β) and similar antiviral effects were observed in the context of subgenomic DENV and ZIKV replicons, these compounds appear to inhibit viral RNA replication in a manner that is independent of their known effects on estrogen receptor signaling. Taken together, quinestrol, raloxifene hydrochloride, and structurally related analogues warrant further investigation as potential therapeutics for treatment of flavivirus infections.

Indexed as

Dengue VirusFlavivirusFlavivirus InfectionsZika VirusZika Virus InfectionEstrogen Receptor ModulatorsFemaleHumansPlacentaPregnancyEstrogen Receptor Modulatorsantiviralantiviral agentsdengue virusestrogen receptorflavivirushigh-throughput screeningWest Nile virusZika virus

Identifiers

PMID32482672
PMCPMC7526829
OpenAlexW3029837890

What OpenQuestion holds

Textmetadata
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.