Evidence map›Paper›PMID 38800832›Full record

ArticleFrontiers in cellular and infection microbiology2024

Unlocking the antiviral potential of rosmarinic acid against chikungunya virus via IL-17 signaling pathway.

Xinfei Liao, Jialiang Xin, Ziping Yu, Weiming Yan, Chenghui Li, Liang Cao, He Zhang, Wei Wang

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Antiviral Activity and Underlying Mechanism ofMolecules (Basel, Switzerland) · 2025
    Article
  4. 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

8 authors.

Xinfei LiaoWenzhou Polytechnic, Wenzhou, Zhejiang, China.
Jialiang XinInstitute of Virology, Wenzhou University, Wenzhou, Zhejiang, China.
Ziping YuInstitute of Virology, Wenzhou University, Wenzhou, Zhejiang, China.
Weiming YanInstitute of Virology, Wenzhou University, Wenzhou, Zhejiang, China.
Chenghui LiCollege of Agriculture, Yanbian University, Yanji, Jilin, China.
Liang CaoChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, Jilin, China.
He ZhangChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, Jilin, China.
Wei WangInstitute of Virology, Wenzhou University, Wenzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Chikungunya virus is an Methods: This study employed network pharmacology to predict and verify the molecular targets and pathways associated with ROSA in the context of CHIKV. The analysis outcomes were further validated using molecular docking and Results: The analysis of CHIKV targets using the Kyoto Encyclopedia of Genes and Genomes and MCODE identified IL-17 as an important pathogenic pathway in CHIKV infection. Among the 30 targets of ROSA against CHIKV, nearly half were found to be involved in the IL-17 signaling pathway. This suggests that ROSA may help the host in resisting CHIKV invasion by modulating this pathway. Molecular docking validation results showed that ROSA can stably bind to 10 core targets out of the 30 identified targets. In an Conclusion: This study provides the first confirmation of the efficacy of ROSA in suppressing CHIKV infection through the IL-17 signaling pathway. The findings warrant further investigation to facilitate the development of ROSA as a potential treatment for CHIKV infection.

Indexed as

Antiviral AgentsChikungunya FeverChikungunya virusCinnamatesDepsidesInterleukin-17Molecular Docking SimulationRosmarinic AcidSignal TransductionAnimalsHEK293 CellsHumansNetwork PharmacologyVirus ReplicationAntiviral AgentsCinnamatesDepsidesInterleukin-17Rosmarinic Acidchikungunya virusIL-17 signaling pathwaymolecular dockingnetwork pharmacologyrosmarinic acid

Identifiers

PMID38800832
PMCPMC11127627

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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.