School of Life Sciences, Shanghai University, Shanghai 200444, PR China.
Anticancer Agents Med Chem. 2010 Sep;10(7):564-70. doi: 10.2174/187152010793498654.
Bisdioxopiperazine (Biz) compounds, including ICRF-154 and razoxane (ICRF-159, Raz), are anticancer agents developed in the UK specifically targeting tumor metastases. Further three bisdioxopiperazine derivatives, bimolane (Bim), probimane (Pro) and MST-16, have been synthesized at the Shanghai Institute of Materia Medica, Chinese Academy of Sciences, PR China after 1980. Since metastases, the prevailing deadliest pathologic feature of cancer in clinics, have been the main obstacle in cancer therapy, antimetastatic effects and mechanisms of Biz compounds are interesting and significant topics of all time for researchers undergoing the investigations of metastases biology, treatments and patho-physiology. This review addresses and highlights the different inhibitions against metastases in vivo and molecular mechanisms in vitro of Biz compounds especially relating to the inhibitions of tumor metastasis including pathways of inhibitions against angiogenesis, topoisomerase II, calmodulin, sialic acid, fibrinogen, cell-movement and so on. We argue hererin that the systematic exploration of antimetastatic activity and mechanisms of Biz compounds seems to be a shortcut for a final solution of cancer therapy in the future.
双二氧哌嗪(Biz)类化合物,包括 ICRF-154 和拉佐烷(ICRF-159,Raz),是英国专门针对肿瘤转移开发的抗癌药物。20 世纪 80 年代以后,中国科学院上海药物研究所又合成了另外三种双二氧哌嗪衍生物:比拉烷(Bim)、前比拉烷(Pro)和 MST-16。由于转移是临床癌症最致命的病理特征,一直是癌症治疗的主要障碍,Biz 类化合物的抗转移作用和机制一直是从事转移生物学、治疗和病理生理学研究的研究人员感兴趣和具有重要意义的课题。本综述讨论并强调了 Biz 类化合物在体内对转移的不同抑制作用和体外的分子机制,特别是与肿瘤转移抑制有关的机制,包括抑制血管生成、拓扑异构酶 II、钙调蛋白、唾液酸、纤维蛋白原、细胞运动等途径。我们认为,系统探索 Biz 类化合物的抗转移活性和机制似乎是未来癌症治疗最终解决方案的捷径。