Chemical Profiling, Antioxidant, and Antiproliferative Activities of Algerian Cistus creticus L. Leaf Extracts: Evidence from In Vitro and In Silico Studies

化学 橙皮苷 DPPH 槲皮素 乙酸乙酯 阿布茨 木犀草素 抗氧化剂 芹菜素 传统医学 芦丁 对接(动物) 类黄酮 山奈酚 生物化学 替代医学 护理部 病理 医学
作者
Yacine Aouiffat,Farouk Benaceur,Boulanouar Bakchiche,Imededdine Kadi,Fathi Berrabah,Hicham Gouzi,Sanaa K. Bardaweel,Ashok K. Shakya,Asmaa S. Mohamed,Mosad A. Ghareeb
出处
期刊:Current Topics in Medicinal Chemistry [Bentham Science Publishers]
卷期号:25 (15): 1882-1904 被引量:3
标识
DOI:10.2174/0115680266345222250109102407
摘要

Background: Research into oxidative stress, cancer, and natural products revealed promising avenues for therapeutic intervention. Natural products are considered potent pharmaceuticals in combating oxidative stress and its relationship with cancer. Methods: This study was carried out to evaluate the chemical profile and antioxidant activities using DPPH, ABTS, Phenanthroline, Cupric, Phosphomolybdenum, FRAP, Hydroxyl, Iron chelation in vitro assays, and anticancer properties by MTT method of Cistus creticus extracts. The chemical composition was determined using the LC/MS-MS technique. Therefore, in silico methods, particularly molecular docking and dynamic simulation were applied for molecular interaction analysis Results: The obtained results revealed a wide variety of phenolic compounds in all studied fractions, in their qualitative and quantitative distribution. In most antioxidant assays, the butanol and ethyl acetate extracts exhibited the most effective effects, followed by the aqueous extract, while the petroleum ether and chloroform fractions exhibited much lower activity in comparison with standards. In parallel, ethyl acetate, n-butanol, and chloroform extracts exhibited potent antiproliferative activity against T47D and A549 cell lines, while the aqueous extract showed an IC50 in the range of mg/ml. Moreover, the analysis of interactions identified compounds against particular targets in studied cell lines using molecular docking showed a great affinity, especially for the ligands Hesperidin, Luteolin-7-O-glucoside and Rutin. Also, the molecular dynamic simulation of the interacting complexes Hesperidin-mTOR, Lutin-EGFR and Apigenin-HER2 revealed precise interaction, providing insights into their stability and dynamic behavior. Furthe Conclusion: These findings confirmed the potential of Algerian Cistus creticus L. leaf extracts as promising therapeutic molecules for combating oxidative stress and cancer.
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