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7-羟基香豆素与顺铂衍生的铂(IV)配合物的联合作用通过多种作用机制增强了细胞毒性。

Combination of 7-hydroxycoumarin in a platinum(IV) complex derived from cisplatin enhanced cytotoxicity with multiple mechanisms of action.

机构信息

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.

出版信息

J Inorg Biochem. 2018 Sep;186:17-23. doi: 10.1016/j.jinorgbio.2018.05.015. Epub 2018 May 23.

Abstract

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.

摘要

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。

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