Li Jing, Risinger April L, Mooberry Susan L
Department of Pharmacology, University of Texas Health Science Center at San Antonio, TX 78229, United States; Cancer Therapy & Research Center, University of Texas Health Science Center at San Antonio, TX 78229, United States.
Department of Pharmacology, University of Texas Health Science Center at San Antonio, TX 78229, United States; Department of Medicine, University of Texas Health Science Center at San Antonio, TX 78229, United States; Cancer Therapy & Research Center, University of Texas Health Science Center at San Antonio, TX 78229, United States.
Bioorg Med Chem. 2014 Sep 15;22(18):5091-6. doi: 10.1016/j.bmc.2014.01.012. Epub 2014 Jan 15.
This review focuses on a relatively new class of microtubule stabilizers, the taccalonolides. The taccalonolides are highly oxygenated pentacyclic steroids isolated from plants of the genus Tacca. Originally identified in a cell-based phenotypic screen, the taccalonolides have many properties similar to other microtubule stabilizers. They increase the density of interphase microtubules, causing microtubule bundling, and form abnormal multi-polar mitotic spindles leading to mitotic arrest and, ultimately, apoptosis. However, the taccalonolides differ from other microtubule stabilizers in that they retain efficacy in taxane resistant cell lines and in vivo models. Binding studies with the newly identified, potent taccalonolide AJ demonstrated covalent binding to β-tubulin at or near the luminal and/or pore taxane binding site(s) which stabilizes microtubule protofilaments in a unique manner as compared to other microtubule stabilizers. The isolation and semi-synthesis of 21 taccalonolides helped to identify key structure activity relationships and the importance of multiple regions across the taccalonolide skeleton for optimal biological potency.
本综述聚焦于一类相对较新的微管稳定剂——taccalonolides。taccalonolides是从黑三棱属植物中分离出的高度氧化的五环甾体。最初是在基于细胞的表型筛选中被鉴定出来的,taccalonolides具有许多与其他微管稳定剂相似的特性。它们增加间期微管的密度,导致微管成束,并形成异常的多极有丝分裂纺锤体,从而导致有丝分裂停滞,并最终引发细胞凋亡。然而,taccalonolides与其他微管稳定剂的不同之处在于,它们在紫杉烷耐药细胞系和体内模型中仍保持效力。与新鉴定出的强效taccalonolide AJ的结合研究表明,它在管腔和/或孔紫杉烷结合位点处或其附近与β-微管蛋白发生共价结合,与其他微管稳定剂相比,这种结合以独特的方式稳定了微管原纤维。21种taccalonolides的分离和半合成有助于确定关键的构效关系,以及taccalonolide骨架上多个区域对最佳生物学活性的重要性。