Evidence map›Paper›PMID 42581353›Full record

ArticleBMC complementary medicine and therapies2026

Synergistic anti-cancer activity of Artemisia vulgaris L. aqueous extract with cisplatin against A549 lung cancer cell line.

Seham Salah El-Din Elhawary, Hadeel Nabil Ahmed, Mouchira A Choucry, Rasha M Allam, Osama G Mohamed, Kamel Mahmoud, Amira K Elmotayam

Abstract read
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Article in BMC complementary medicine and therapies, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Seham Salah El-Din ElhawaryDepartment of Pharmacognosy, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, Egypt.
Hadeel Nabil AhmedDepartment of Pharmacognosy, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, Egypt.
Mouchira A ChoucryDepartment of Pharmacognosy, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, Egypt.
Rasha M AllamPharmacology Department, Medical Research Institute, National Research Center, 33 El-Bohouth St., Dokki, P.O.12622, Cairo, Egypt.
Osama G MohamedDepartment of Pharmacognosy, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, Egypt.
Kamel Mahmoud *Department of Pharmacognosy, Faculty of Pharmaceutical Sciences & Drug Manufacturing, Misr University for Science and Technology, Giza, Egypt.
Amira K Elmotayam *Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, Egypt. Amira.kamal@pharma.cu.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing resistance and adverse effects associated with conventional chemotherapeutic agents such as cisplatin have prompted the investigation of natural compounds that act synergistically with chemotherapy to combat cancer. This study investigates the cytotoxic effects of an aqueous extract of Artemisia vulgaris L. in conjunction with cisplatin on A549 human lung cancer cells. The research analyzes the phytochemical composition of the extract and its potential mechanisms of action by assessing apoptosis and autophagy. Cytotoxicity studies demonstrated a synergistic interaction between A. vulgaris and cisplatin. We utilized molecular docking to examine the interactions of the extract components with critical proteins involved in these processes.

methodsLiquid chromatography-tandem mass spectrometry (LC-MS/MS) was employed to characterize the phytochemicals in A. vulgaris. A549 cells were subjected to various concentrations of A. vulgaris L. aqueous extract, cisplatin, and their combination. We utilized the SRB assay to assess cell viability and the combination index (CI) analysis to evaluate the synergistic interaction between the two compounds. Molecular docking was performed for selected compounds against apoptotic and autophagic target proteins.

resultsThe combination treatment showed a greater cytotoxic effect than either treatment alone, suggesting a synergistic improvement of anticancer action through the induction of both apoptosis and autophagy. This was manifested by a significant decrease in the IC

conclusionThe results indicated that A. vulgaris L. may potentiate the anticancer effect of cisplatin, potentially allowing dose reduction and minimizing side effects.

Indexed as

Antineoplastic AgentsArtemisiaCisplatinLung NeoplasmsPlant ExtractsA549 CellsApoptosisAutophagyCell SurvivalChromatography, LiquidDrug SynergismHumansMolecular Docking SimulationTandem Mass SpectrometryAntineoplastic AgentsCisplatinPlant ExtractsA549 cellsApoptosisArtemisia vulgaris L.AutophagyCisplatinLung cancer

Identifiers

PMID42581353
PMCPMC13459383

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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.