Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China.
Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China; Jiangsu Province Hi-Tech Key Laboratory for Bio-medical Research, Southeast University, Nanjing 211189, China.
J Inorg Biochem. 2018 Sep;186:17-23. doi: 10.1016/j.jinorgbio.2018.05.015. Epub 2018 May 23.
A novel compound, Cou-platin, composed of 7-hydroxycoumarin and a platinum(IV) moiety derived from cisplatin was designed and synthesized. Significantly, Cou-platin exhibited more potent in vitro antitumor activity against all tested cancer cell lines than that of cisplatin, which was mainly attributed to the liberation of cisplatin and 7-hydroxycoumarin upon reduction with a biomolecular agent. Besides, cellular accumulation of Cou-platin was dramatically increased among several cancer cells in contrast to cisplatin. Flow cytometry study revealed that Cou-platin arrested cell cycle at G2 phase and induced cell apoptosis. Western blots results indicated that it not only activated cell apoptosis pathway, but also inhibited extracellular regulated protein kinases/mitogen-activated protein kinase pathway. In vivo tests showed that Cou-platin, at equimolar dose to cisplatin, could inhibit tumor growth in nude mouse HCT116 tumor xenograft models almost as cisplatin and oxaliplatin, but with less toxicity.
一种新型化合物 Cou-platin 被设计和合成,它由顺铂衍生的 7-羟基香豆素和铂(IV)部分组成。值得注意的是,Cou-platin 对所有测试的癌细胞系的体外抗肿瘤活性均强于顺铂,这主要归因于生物分子试剂还原时释放顺铂和 7-羟基香豆素。此外,Cou-platin 在几种癌细胞中的细胞内积累明显高于顺铂。流式细胞术研究表明,Cou-platin 将细胞周期阻滞在 G2 期并诱导细胞凋亡。Western blot 结果表明,它不仅激活了细胞凋亡途径,还抑制了细胞外调节蛋白激酶/丝裂原活化蛋白激酶途径。体内试验表明,Cou-platin 在等摩尔剂量下对裸鼠 HCT116 肿瘤异种移植模型的肿瘤生长抑制作用几乎与顺铂和奥沙利铂相当,但毒性较小。