Vo Giau Van, Nguyen Thi-Hoai-Thu, Nguyen Thi-Phuong, Do Thi-Hong-Tuoi, Tran Nguyen-Minh-An, Nguyen Huy Truong, Nguyen Thuy Trang
Department of Biomedical Engineering, School of Medicine, Vietnam National University - Ho Chi Minh City (VNU-HCM), Ho Chi Minh City 70000, Vietnam.
Research Center for Genetics and Reproductive Health (CGRH), School of Medicine, Vietnam National University, Ho Chi Minh City (VNU-HCM), Ho Chi Minh City 70000, Vietnam.
Saudi Pharm J. 2022 Sep;30(9):1301-1314. doi: 10.1016/j.jsps.2022.06.018. Epub 2022 Jun 22.
L. () is one of the important medicinal and anticancer enhancer herbs. This plant is commonly used in the preparation of traditional drugs to treat numerous diseases. Inspired by the medicinal properties of this plant, the current study aimed to investigate antiproliferative potential and the primary molecular mechanisms of the apoptotic induction against human HepG2 and MCF-7 cell lines, by pure compounds isolated from targeted fractions of which were characterized by NMR, FTIR and HRMS analysis and identified as artemetin (FLV1), vitexicarpin (FLV2), and penduletin (FLV3) compounds. The FLV1, FLV2, and FLV3 compounds were evaluated for the antiproliferative potential against HepG2 and MCF-7 cell lines by cell viability assay and exhibited IC values of 2.3, 23.9 and 5.6 µM and 3.9, 25.8, and 6.4 µM, respectively. In addition, those compounds increased the level of reactive oxygen species production, induced cell death occurred via apoptosis, demonstrated by Annexin V-staining cells, contributed significantly to DNA damage, and led to the activation of caspase3/caspase8 pathways.Additionally, molecular docking was also conducted to rationalize the cancer cells inhibitory and to evaluate the ability of the FLV1, FLV2, and FLV3 compounds to be developed as good drug candidates for cancers treatment.
L.()是重要的药用和抗癌增强草药之一。这种植物常用于制备治疗多种疾病的传统药物。受这种植物药用特性的启发,本研究旨在通过从其靶向馏分中分离出的纯化合物,研究对人肝癌细胞系HepG2和人乳腺癌细胞系MCF - 7的抗增殖潜力以及诱导凋亡的主要分子机制,这些化合物通过核磁共振(NMR)、傅里叶变换红外光谱(FTIR)和高分辨质谱(HRMS)分析进行了表征,并鉴定为青蒿亭(FLV1)、紫铆亭(FLV2)和penduletin(FLV3)化合物。通过细胞活力测定评估了FLV1、FLV2和FLV3化合物对HepG2和MCF - 7细胞系的抗增殖潜力,其IC值分别为2.3、23.9和5.6 μM以及3.9、25.8和6.4 μM。此外,这些化合物增加了活性氧的产生水平,通过膜联蛋白V染色细胞证明诱导细胞通过凋亡发生死亡,对DNA损伤有显著贡献,并导致半胱天冬酶3/半胱天冬酶8途径的激活。此外,还进行了分子对接以合理化对癌细胞的抑制作用,并评估FLV1、FLV2和FLV3化合物作为癌症治疗良好候选药物的开发能力。