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诱导胀亡的环金属化铱(III)配合物

Oncosis-inducing cyclometalated iridium(iii) complexes.

作者信息

Guan Ruilin, Chen Yu, Zeng Leli, Rees Thomas W, Jin Chengzhi, Huang Juanjuan, Chen Zhe-Sheng, Ji Liangnian, Chao Hui

机构信息

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry , School of Chemistry , Sun Yat-Sen University , Guangzhou , 510275 , P. R. China . Email:

College of Pharmacy and Health Sciences , St. John's University , New York , NY 11439 , USA.

出版信息

Chem Sci. 2018 May 3;9(23):5183-5190. doi: 10.1039/c8sc01142g. eCollection 2018 Jun 21.

Abstract

Oncosis is a non-apoptotic form of programmed cell death (PCD), which differs from apoptosis in both morphological changes and inner pathways, and might hold the key to defeating a major obstacle in cancer therapy - drug-resistance, which is often a result of the intrinsic apoptosis resistance of tumours. However, despite the fact that the term "oncosis" was coined and used much earlier than apoptosis, little effort has been made to discover new drugs which can initiate this form of cell death, in comparison to drugs inducing apoptosis or any other type of PCD. So herein, we present the synthesis of a series of mitochondria-targeting cyclometalated Ir(iii) complexes, which activated the oncosis-specific protein porimin and calpain in cisplatin-resistant cell line A549R, and determined their cytotoxicity against a wide range of drug-resistant cancer types. To the best of our knowledge, these complexes are the very first metallo-components to induce oncosis in drug-resistant cancer cells.

摘要

胀亡是一种程序性细胞死亡(PCD)的非凋亡形式,在形态变化和内在途径上均与凋亡不同,可能是攻克癌症治疗中一个主要障碍——耐药性的关键,而肿瘤的内在凋亡抗性往往导致耐药性。然而,尽管“胀亡”一词的提出和使用比凋亡早得多,但与诱导凋亡或任何其他类型PCD的药物相比,人们在发现能够引发这种细胞死亡形式的新药方面付出的努力很少。因此,在此我们展示了一系列靶向线粒体的环金属化铱(III)配合物的合成,这些配合物在顺铂耐药细胞系A549R中激活了胀亡特异性蛋白孔蛋白和钙蛋白酶,并测定了它们对多种耐药癌症类型的细胞毒性。据我们所知,这些配合物是首批在耐药癌细胞中诱导胀亡的金属成分。

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