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单功能铂(II)化合物——新型铂基抗癌药物设计范式的转变

Monofunctional Platinum (PtII) Compounds - Shifting the Paradigm in Designing New Pt-based Anticancer Agents.

作者信息

Chong Shu Xian, Au-Yeung Steve Chik Fun, To Kenneth Kin Wah

机构信息

Department of Chemistry, The Chinese University of Hong Kong, Sha Tin, N.T., Hong Kong SAR.

School of Pharmacy, The Chinese University of Hong Kong, Sha Tin, N.T., Hong Kong SAR.

出版信息

Curr Med Chem. 2016;23(12):1268-85. doi: 10.2174/0929867323666160311114509.

Abstract

Platinum (Pt)-based anticancer drugs, exemplified by cisplatin, are key components in combination chemotherapy. However, their effective use is hindered by toxicity and emergence of drug resistance. They bind to DNA and mainly form the Pt-GG diadduct, subsequently leading to apoptosis to mediate cell death. On the other hand, the Pt drug -proteins and -metabolites interactions, which involve the reaction between Pt and sulfur sites located in protein side chains and important bionucleophiles (e.g., glutathione), are responsible for the toxicity and drug resistance problem. Therefore, carefully designed coordinating ligands may provide the means of fine tuning the electronic environment around the core Pt atom and allow the resulting Pt compounds to bind with the DNA in a different manner. This may produce alternative cell death mechanisms in cancer cells, thereby circumventing Pt resistance. This article reviewed the recent development in monofunctional Pt complexes and their prospects in becoming a new generation of anticancer drugs.

摘要

以顺铂为代表的铂(Pt)基抗癌药物是联合化疗的关键组成部分。然而,它们的有效使用受到毒性和耐药性出现的阻碍。它们与DNA结合,主要形成Pt-GG二元加合物,随后导致细胞凋亡以介导细胞死亡。另一方面,铂药物与蛋白质和代谢物的相互作用,涉及铂与位于蛋白质侧链的硫位点和重要生物亲核试剂(如谷胱甘肽)之间的反应,是毒性和耐药性问题的原因。因此,精心设计的配位配体可能提供微调核心铂原子周围电子环境的方法,并使所得的铂化合物以不同方式与DNA结合。这可能在癌细胞中产生替代的细胞死亡机制,从而规避铂耐药性。本文综述了单功能铂配合物的最新进展及其成为新一代抗癌药物的前景。

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