Department of Pharmacology, The University of Texas Health Science Center at San Antonio, 78229, United States.
Cancer Lett. 2010 May 1;291(1):14-9. doi: 10.1016/j.canlet.2009.09.020. Epub 2009 Oct 31.
Nature remains an important source for new anticancer drugs. Numerous microtubule-targeting agents currently approved or in clinical development, including paclitaxel, vinblastine, vincristine, colchicine and combretastatin, are plant-derived compounds. The microtubule stabilizing properties of the taccalonolides were discovered as a part of a program to identify new microtubule stabilizers from natural sources. The taccalonolides are unique among all other agents in this class in that they stabilize microtubules through a mechanism of action that does not involve direct tubulin binding. Herein we review the discovery and isolation of the taccalonolides, their biological activities in vitro and in vivo and their potential advantages over clinically used microtubule stabilizers. We also discuss the challenges in formulation and supply that will need to be solved before the taccalonolides can become candidates for clinical development.
天然产物仍然是新型抗癌药物的重要来源。目前已批准或处于临床开发阶段的许多微管靶向药物,包括紫杉醇、长春碱、长春新碱、秋水仙碱和 combretastatin,都是植物来源的化合物。作为从天然来源中寻找新型微管稳定剂计划的一部分,人们发现了 taccalonolide 具有稳定微管的特性。与该类中的其他所有药物不同,taccalonolide 通过一种不涉及直接微管蛋白结合的作用机制稳定微管。本文综述了 taccalonolide 的发现和分离、它们在体外和体内的生物活性以及它们相对于临床使用的微管稳定剂的潜在优势。我们还讨论了在 taccalonolide 成为临床开发候选药物之前需要解决的制剂和供应方面的挑战。