Villegas Cecilia, González-Chavarría Iván, Burgos Viviana, Cabrera-Pardo Jaime R, Schmidt Bernd, Paz Cristian
Laboratory of Natural Products & Drug Discovery, Center CEBIM, Department of Basic Sciences, Faculty of Medicine, Universidad de La Frontera, Temuco 4780000, Chile.
Departamento de Fisiopatología, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción 4070386, Chile.
J Xenobiot. 2025 Mar 18;15(2):45. doi: 10.3390/jox15020045.
Germacranes are a type of sesquiterpene lactones with anti-inflammatory and cytotoxic properties against cancer cell lines. In this in vitro study, erioflorin and erioflorin acetate were isolated and purified from the leaves of Lindl (Mitique or Mitriu), a shrub endemic to Chile and traditionally used in Mapuche medicine to treat urinary and digestive disorders. Their effects on advanced prostate cancer cell lines (DU-145 and 22Rv1) were evaluated. Cytotoxicity was assessed using real-time cell death and clonogenic assays. Apoptosis was determined by measuring reactive oxygen species (ROS), mitochondrial membrane potential (ΔΨm), and apoptotic cell percentage through flow cytometry. Gene expression of and was analyzed via RT-qPCR, while NF-κB activation was studied in DU-145 cells and human monocytic NF-κB reporter assays using LPS stimulation and alkaline phosphatase activity quantification. Erioflorin acetate exhibited the highest cytotoxicity, with IC values of 35.1 µM (22Rv1) and 27.3 µM (DU-145), compared to erioflorin, which had IC values of 50.3 µM and 56.5 µM, respectively. Both compounds increased ROS levels, reduced ΔΨm, and induced apoptosis. RT-qPCR analysis revealed that erioflorin elevated the ratio, and both compounds inhibited NF-κB activation by preventing IκBα phosphorylation. In conclusion, the findings demonstrate that erioflorin and erioflorin acetate exert significant in vitro cytotoxic and cytostatic effects on prostate cancer cells, supporting their potential as natural candidates for prostate cancer therapy.
吉马烷型倍半萜内酯是一类具有抗炎和对癌细胞系具有细胞毒性的物质。在这项体外研究中,从智利特有的一种灌木Lindl(Mitique或Mitriu)的叶子中分离并纯化了eriophyllin和乙酸eriophyllin,该灌木在马普切医学中传统上用于治疗泌尿和消化系统疾病。评估了它们对晚期前列腺癌细胞系(DU-145和22Rv1)的影响。使用实时细胞死亡和克隆形成试验评估细胞毒性。通过流式细胞术测量活性氧(ROS)、线粒体膜电位(ΔΨm)和凋亡细胞百分比来确定细胞凋亡。通过RT-qPCR分析 和 的基因表达,同时在DU-145细胞和人单核细胞NF-κB报告基因试验中使用LPS刺激和碱性磷酸酶活性定量研究NF-κB激活。与eriophyllin的IC值分别为50.3 µM和56.5 µM相比,乙酸eriophyllin表现出最高的细胞毒性,其IC值分别为35.1 µM(22Rv1)和27.3 µM(DU-145)。两种化合物均增加了ROS水平,降低了ΔΨm,并诱导了细胞凋亡。RT-qPCR分析显示eriophyllin提高了 比率,并且两种化合物都通过阻止IκBα磷酸化来抑制NF-κB激活。总之,研究结果表明eriophyllin和乙酸eriophyllin在体外对前列腺癌细胞具有显著的细胞毒性和细胞抑制作用,支持它们作为前列腺癌治疗天然候选物的潜力。