Cancer Science Institute of Singapore, National University of Singapore, Singapore.
Department of Pharmacology, National University Health System, Singapore.
Cancer. 2019 Jun 1;125(11):1789-1798. doi: 10.1002/cncr.32069. Epub 2019 Apr 1.
Deguelin is a rotenoid compound that exists in abundant quantities in the bark, roots, and leaves of the Leguminosae family of plants. An analysis of evidence from both in vitro and in vivo studies suggests that deguelin displays potent anticancer activity against multiple cancer types and exhibits chemopreventive potential in Akt-inducible transgenic mouse models. Deguelin appears to impede carcinogenesis by enhancing cell apoptosis and hindering malignant transformation and tumor cell propagation. Crucial oncogenic pathways likely targeted by deguelin include the epithelial-to-mesenchymal transition; angiogenesis-related pathways; and the phosphoinositide 3-kinase/Akt, Wnt, epidermal growth factor receptor, c-Met, and hedgehog signal transduction cascades. This review article provides a comprehensive summary of current preclinical research featuring deguelin as a leading chemotherapeutic and chemopreventive compound, and it highlights the importance of identifying companion molecular biomarkers and performing systemic pharmacokinetic studies for accelerating the process of developing deguelin as a clinical anticancer agent.
冬凌草甲素是一种在豆科植物的树皮、根和叶中大量存在的裂环烯醚萜类化合物。来自体外和体内研究的证据分析表明,冬凌草甲素有针对多种癌症类型的强大抗癌活性,并在 Akt 诱导的转基因小鼠模型中显示出化学预防潜力。冬凌草甲素似乎通过增强细胞凋亡、阻碍恶性转化和肿瘤细胞增殖来阻碍癌变。冬凌草甲素可能靶向的关键致癌途径包括上皮间质转化、血管生成相关途径以及磷酸肌醇 3-激酶/ Akt、Wnt、表皮生长因子受体、c-Met 和 Hedgehog 信号转导级联。本文综述了以冬凌草甲素为主要化疗和化学预防化合物的当前临床前研究,强调了确定伴随分子生物标志物和进行系统药代动力学研究以加速将冬凌草甲素开发为临床抗癌药物的重要性。