Evidence map›Paper›PMID 37893127›Full record

ArticleBiomedicines2023

The Antiviral Activity of Varenicline against Dengue Virus Replication during the Post-Entry Stage.

Ching-Lin Lin, Yan-Tung Kiu, Ju-Ying Kan, Yu-Jen Chang, Ping-Yi Hung, Chih-Hao Lu, Wen-Ling Lin, Yow-Wen Hsieh, Jung-Yie Kao, Nien-Jen Hu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

11 authors at 4 institutions in 1 country.

Ching-Lin LinInstitute of Biochemistry, College of Life Sciences, National Chung Hsing University, Taichung 40227, Taiwan.
Yan-Tung KiuDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404328, Taiwan.
Ju-Ying KanDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404328, Taiwan.
Yu-Jen ChangThe Ph.D. Program of Biotechnology and Biomedical Industry, China Medical University, Taichung 404328, Taiwan.
Ping-Yi HungDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404328, Taiwan.
Chih-Hao LuInstitute of Bioinformatics and Systems Biology, National Yang Ming Chiao Tung University, Hsinchu City 30010, Taiwan.
Wen-Ling LinDepartment of Pharmacy, China Medical University Hospital, Taichung 404328, Taiwan.ORCID 0000-0002-9937-6782
Yow-Wen HsiehDepartment of Pharmacy, China Medical University Hospital, Taichung 404328, Taiwan.
Jung-Yie KaoInstitute of Biochemistry, College of Life Sciences, National Chung Hsing University, Taichung 40227, Taiwan.
Nien-Jen HuInstitute of Biochemistry, College of Life Sciences, National Chung Hsing University, Taichung 40227, Taiwan.ORCID 0000-0002-0917-0677
Cheng-Wen LinDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404328, Taiwan.ORCID 0000-0003-0165-2652
Asia University · TWChina Medical University · TWNational Chung Hsing University · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue virus (DENV) poses a significant global health challenge, with millions of cases each year. Developing effective antiviral drugs against DENV remains a major hurdle. Varenicline is a medication used to aid smoking cessation, with anti-inflammatory and antioxidant effects. In this study, varenicline was investigated for its antiviral potential against DENV. This study provides evidence of the antiviral activity of varenicline against DENV, regardless of the virus serotype or cell type used. Varenicline demonstrated dose-dependent effects in reducing viral protein expression, infectivity, and virus yield in Vero and A549 cells infected with DENV-1 and DENV-2, with EC50 values ranging from 0.44 to 1.66 μM. Time-of-addition and removal experiments demonstrated that varenicline had a stronger inhibitory effect on the post-entry stage of DENV-2 replication than on the entry stage, as well as the preinfection and virus attachment stages. Furthermore, cell-based trans-cleavage assays indicated that varenicline dose-dependently inhibited the proteolytic activity of DENV-2 NS2B-NS3 protease. Docking models revealed the formation of hydrogen bonds and van der Waals forces between varenicline and specific residues in the DENV-1 and DENV-2 NS2B-NS3 proteases. These results highlight the antiviral activity and potential mechanism of varenicline against DENV, offering valuable insights for further research and development in the treatment of DENV infection.

Indexed as

antiviralcleavage assaydengue virusNS2B-NS3 proteasepost entryvarenicline

Identifiers

PMID37893127
PMCPMC10604274
OpenAlexW4387572786

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.