Evidence map›Paper›PMID 41146238›Full record

ArticleVirology journal2025

Curcumin-like diarylpentanoid analogues exhibit antiviral and anti-inflammatory activities in influenza A virus-infected A549 lung epithelial cells by inhibiting multiple retinoic acid-inducible gene I (RIG-I)-mediated pathways.

Kong Yen Liew, Hui-Yee Chee, Faridah Abas, Sze Wei Leong, Hanis Hazeera Harith, Ming-Tatt Lee, Mohd Roslan Sulaiman, Chau Ling Tham

Abstract read
In one paragraph

Article in Virology journal, 2025. 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
–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

1 citing paper in PubMed.

  1. Review
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.

Kong Yen LiewDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Hui-Yee CheeDepartment of Medical Microbiology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Faridah AbasDepartment of Food Science, Faculty of Food Science and Technology, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Sze Wei LeongDepartment of Chemistry, Faculty of Science, Universiti Malaya, 50603, Kuala Lumpur, Malaysia.
Hanis Hazeera HarithDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Ming-Tatt LeeUCSI Wellbeing Research Centre, UCSI University, 56000, Kuala Lumpur, Malaysia.
Mohd Roslan SulaimanDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Chau Ling ThamDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia. chauling@upm.edu.my.

Funding

Ministry of Higher Education Malaysia Fundamental Research Grant Scheme (FRGS) FRGS/1/2023/SKK15/UPM/02/3
6 · The paper itself

Abstract

Influenza A virus (IAV) causes seasonal epidemics and occasionally pandemics. Curcumin, a well-known phytochemical, has been reported to exhibit anti-IAV effects; however, most studies were not comprehensive and utilized Mardin-Darby canine kidney (MDCK) cells. Curcumin-like diarylpentanoid analogues, namely 2-benzoyl-6-(3,4-dihydroxybenzylidene)cyclohexen-1-ol (BDHBC) and 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one (DHHPD), exhibit improved drug-like properties, including increased solubility and stability, along with stronger antiviral effects against rhinovirus (RV). Thus, this study evaluates the antiviral and anti-inflammatory activities of BDHBC and DHHPD using A549 lung epithelial cells infected with influenza A/Puerto Rico/8/34 (H1N1), and compared their antiviral effects with curcumin in different treatment modes (pre-, co- and post-treatment). Like curcumin, BDHBC and DHHPD significantly reduced virus yield in the post-treatment mode and exhibited direct virucidal activity. Post-treatment with BDHBC and DHHPD also significantly suppressed viral replication as well as pro-inflammatory cytokines (IL-6, IL-8 and IP-10) and interferons (IFN-β and IFN-λ1) at both the gene and protein levels. The stronger antiviral and anti-inflammatory effects of DHHPD were attributed to its inhibition of multiple retinoic acid-inducible gene I (RIG-I)-mediated signalling pathways, including NF-κB, AP-1, MAPKs (p38 and Erk1/2), IRF3 and Akt. Only some of these pathways were affected by BDHBC treatment. Neither compound affected RIG-I or IRF7 expression, which is consistent with their lack of impact on Stat1 activation. Interestingly, DHHPD also demonstrated significant prophylactic effect against IAV infection, which was not observed for BDHBC and curcumin. In conclusion, BDHBC and DHHPD inhibit IAV replication and cytokine responses by targeting host signalling pathways. Further investigation in vivo is required.

Indexed as

Anti-Inflammatory AgentsAntiviral AgentsCurcuminDEAD Box Protein 58Epithelial CellsInfluenza A virusInfluenza A Virus, H1N1 SubtypeA549 CellsAnimalsCytokinesDogsHumansMadin Darby Canine Kidney CellsReceptors, ImmunologicSignal TransductionVirus ReplicationAnti-Inflammatory AgentsAntiviral AgentsCurcuminCytokinesDEAD Box Protein 58Receptors, ImmunologicRIGI protein, humanAntiviralCurcuminCytokineDiarylpentanoid analogueH1N1Influenza A virusRetinoic acid-inducible gene I (RIG-I)

Identifiers

PMID41146238
PMCPMC12557979

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LicenceCC BY-NC-ND
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Registered trials

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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.