Discovery of Sesquiterpene Lactones with Cytotoxicity from the Herb of Youngia japonica

化学 细胞毒性 细胞毒性T细胞 细胞凋亡 倍半萜 立体化学 细胞周期蛋白D1 倍半萜内酯 细胞周期 癌细胞 鬼臼毒素 生物化学 体外 癌症 生物 遗传学
作者
Xiansheng Ye,kuan lin,xiaoqing tao,jinting shang,Yuran Gui,shuxiu zhu,le zhou,Yiyuan Xia,Wei Liu,Binlian Sun,Hai‐Feng Chen,Xiji Shu
出处
期刊:Chemistry & Biodiversity [Wiley]
标识
DOI:10.1002/cbdv.202401063
摘要

In the process of searching for anti‐breast cancer agents, five sesquiterpene lactones (1‐5), including two previously undescribed ones, yjaponica B‐C (1‐2), were isolated from the herb of Youngia japonica. Their structures were elucidated by spectroscopic data analyses and Marfey’s method. Cytotoxic activities of all compounds against A549, U87, and 4T1 cell lines were tested using the CCK8 assay. The result showed that compound 3 possessed the highest cytotoxic activity against 4T1 cells with an IC50 value of 10.60 μM. Furthermore, compound 3 distinctly induced apoptosis, inhibited immigration, and blocked the cell cycle of 4T1 cells. In addition, compound 3 induced the production of reactive oxygen species. Further anticancer mechanism studies showed that compound 3 significantly upregulated expression of the cleaved caspase 3 and PARP, whereas it downregulated the expression of Bcl‐2, cyclin D1, cyclin A2, CDK4, and CDK2. Taken together, our results demonstrate that compound 3 has a high potential of being used as a leading compound for the discovery of new anti‐breast cancer agent.
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