Johnson Lorelei, Goping Ing Swie, Rieger Aja, Mane Jonathan Y, Huzil Torin, Banerjee Asok, Luduena Richard, Hassani Bashar, Winter Philip, Tuszynski Jack A
Department of Oncology, University of Alberta, Edmonton, Alberta, Canada.
Department of Biochemistry, University of Alberta, Edmonton, Alberta, Canada.
Curr Top Med Chem. 2017;17(22):2538-2558. doi: 10.2174/1568026617666170104143618.
In this paper we provide an overview of the status of various colchicine derivatives in preclinical development with special focus on their anti-cancer activity. We discuss several groups of compounds that have been designed to differentially bind with specific affinities for tubulin β isotypes, especially in regard to βIII, which is commonly over-expressed in cancer. Computational prediction, protein-based and cell-based assays are summarized as well as some animal tests conducted on these compounds. It is concluded that an untapped potential exists for exploiting the colchicine scaffold as a pharmacophore with the possibility of increasing its affinity for tubulin isotypes overexpressed in cancer and decreasing it for normal cells thereby widening the therapeutic window.
在本文中,我们概述了秋水仙碱各种衍生物在临床前开发中的状况,特别关注它们的抗癌活性。我们讨论了几组被设计用于以特定亲和力与微管蛋白β亚型特异性结合的化合物,特别是针对βIII,它在癌症中通常过度表达。总结了计算预测、基于蛋白质和基于细胞的测定方法,以及对这些化合物进行的一些动物试验。得出的结论是,利用秋水仙碱支架作为药效团存在尚未开发的潜力,有可能增加其对癌症中过度表达的微管蛋白亚型的亲和力,并降低对正常细胞的亲和力,从而扩大治疗窗口。