Yacine Aouiffat, Farouk Benaceur, Boulanouar Bakchiche, Imededdine Kadi, Fathi Berrabah, Hicham Gouzi, Sanaa K Bardaweel, Ashok K Shakya, Asmaa S Mohamed, Mosad A Ghareeb
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Therefore, in silico methods, particularly molecular docking and dynamic simulation were applied for molecular interaction analysis.</p><p><strong>Results: </strong>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. 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引用次数: 0
摘要
背景:对氧化应激、癌症和天然产物的研究揭示了治疗干预的有希望的途径。天然产物被认为是对抗氧化应激及其与癌症关系的有效药物。方法:采用DPPH、ABTS、菲罗啉、铜、磷钼、FRAP、羟基、铁螯合等体外测定方法,评价其化学性质和抗氧化活性,并采用MTT法测定其抗癌活性。采用LC/MS-MS技术测定其化学成分。因此,分子相互作用的分析主要采用了分子对接和动态模拟等方法。结果:所得到的结果显示,所研究的各组分中酚类化合物的种类繁多,其定性和定量分布也很广泛。在大多数抗氧化试验中,丁醇和乙酸乙酯萃取物表现出最有效的效果,其次是水萃取物,而石油醚和氯仿萃取物表现出比标准低得多的活性。同时,乙酸乙酯、正丁醇和氯仿提取物对T47D和A549细胞株具有较强的抗增殖活性,而水提物的IC50值在mg/ml范围内。此外,利用分子对接方法对所鉴定的化合物与所研究细胞系中特定靶点的相互作用进行分析,发现它们具有很强的亲和力,特别是对配体橙皮苷、木犀草素-7- o -糖苷和芦丁。此外,相互作用复合物Hesperidin-mTOR, Lutin-EGFR和Apigenin-HER2的分子动力学模拟揭示了精确的相互作用,为其稳定性和动态行为提供了见解。此外,所研究的配体表现出有趣的药代动力学性质,没有毒性报道。结论:这些研究结果证实了阿尔及利亚山茱萸叶提取物作为抗氧化应激和癌症治疗分子的潜力。
Chemical Profiling, Antioxidant, and Antiproliferative Activities of Algerian Cistus creticus L. Leaf Extracts: Evidence from In vitro and In Silico Studies.
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. Furthermore, the studied ligand exhibited interesting pharmacokinetic properties with no reported toxicity.
Conclusion: These findings confirmed the potential of Algerian Cistus creticus L. leaf extracts as promising therapeutic molecules for combating oxidative stress and cancer.
期刊介绍:
Current Topics in Medicinal Chemistry is a forum for the review of areas of keen and topical interest to medicinal chemists and others in the allied disciplines. Each issue is solely devoted to a specific topic, containing six to nine reviews, which provide the reader a comprehensive survey of that area. A Guest Editor who is an expert in the topic under review, will assemble each issue. The scope of Current Topics in Medicinal Chemistry will cover all areas of medicinal chemistry, including current developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, compound diversity measurements, drug absorption, drug distribution, metabolism, new and emerging drug targets, natural products, pharmacogenomics, and structure-activity relationships. Medicinal chemistry is a rapidly maturing discipline. The study of how structure and function are related is absolutely essential to understanding the molecular basis of life. Current Topics in Medicinal Chemistry aims to contribute to the growth of scientific knowledge and insight, and facilitate the discovery and development of new therapeutic agents to treat debilitating human disorders. The journal is essential for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important advances.