Nam Nguyen-Hai
Department of Biomedical Sciences, College of Pharmacy, University of Rhode Island, RI 02881, USA.
Curr Med Chem. 2003 Sep;10(17):1697-722. doi: 10.2174/0929867033457151.
Tubulin protein is a major target for anticancer drug discovery. As a result, antimitotic agents constitute an important class of the current anticancer drugs. Hundreds of tubulin inhibitors, naturally occurring, semisynthetic or synthetic, have been reported. Among these, combretastatin A-4 (CA-4), isolated from a South African tree Combretum caffrum, is one of the most potent antimitotic agents. CA-4 shows strong cytotoxicity against a variety of cancer cells, including multi-drug resistant cancer cell lines. It has also been demonstrated to exert highly selective effects in proliferating endothelial cells. CA-4 disodium phosphate (CA4DP), a water-soluble prodrug of CA-4, shows potent antivascular and antitumor effects in a wide variety of preclinical tumor models. Consequently, a number of CA-4 analogues has been synthesized and evaluated. In this paper, the structure-activity relationships and pharmacological properties of the CA-4 derivatives as a class of potent antimitotic anticancer agents are reviewed and discussed.
微管蛋白是抗癌药物研发的主要靶点。因此,抗有丝分裂剂构成了当前抗癌药物的一个重要类别。已报道了数百种天然存在、半合成或合成的微管蛋白抑制剂。其中,从南非树木南非风车子中分离出的康普瑞他汀A-4(CA-4)是最有效的抗有丝分裂剂之一。CA-4对多种癌细胞,包括多药耐药癌细胞系,显示出强大的细胞毒性。它还被证明在增殖的内皮细胞中发挥高度选择性作用。CA-4磷酸二钠(CA4DP)是CA-4的水溶性前药,在多种临床前肿瘤模型中显示出强大的抗血管和抗肿瘤作用。因此,已经合成并评估了许多CA-4类似物。本文对CA-4衍生物作为一类有效的抗有丝分裂抗癌剂的构效关系和药理特性进行了综述和讨论。