Tong Ka-Chung, Hu Di, Wan Pui-Ki, Lok Chun-Nam, Che Chi-Ming
State Key Laboratory of Synthetic Chemistry, Department of Chemistry, The University of Hong Kong, Hong Kong, China.
Laboratory for Synthetic Chemistry and Chemical Biology, Health@InnoHK, Hong Kong, China.
Front Chem. 2020 Nov 6;8:587207. doi: 10.3389/fchem.2020.587207. eCollection 2020.
The use of gold in medicine has a long history. Recent clinical applications include anti-inflammatory agents for the treatment of rheumatoid arthritis (chrysotherapy), and is currently being developed as potential anticancer chemotherapeutics. Gold(III), being isoelectronic to platinum(II) as in cisplatin, is of great interest but it is inherently unstable and redox-reactive under physiological conditions. Coordination ligands containing C and/or N donor atom(s) such as porphyrin, pincer-type cyclometalated and/or N-heterocyclic carbene (NHC) can be employed to stabilize gold(III) ion for the preparation of anticancer active compounds. In this review, we described our recent work on the anticancer properties of gold(III) compounds and the identification of molecular targets involved in the mechanisms of action. We also summarized the chemical formulation strategies that have been adopted for the delivery of cytotoxic gold compounds, and for ameliorating the toxicity.
金在医学中的应用历史悠久。近期的临床应用包括用于治疗类风湿性关节炎的抗炎剂(金疗法),并且目前正在开发其作为潜在的抗癌化学治疗剂。金(III)与顺铂中的铂(II)具有等电子体性质,备受关注,但它在生理条件下本质上不稳定且具有氧化还原活性。含有碳和/或氮供体原子的配位配体,如卟啉、钳型环金属化和/或N-杂环卡宾(NHC),可用于稳定金(III)离子以制备抗癌活性化合物。在本综述中,我们描述了我们最近关于金(III)化合物抗癌特性的研究工作以及对作用机制中涉及的分子靶点的鉴定。我们还总结了为递送细胞毒性金化合物和改善毒性而采用的化学制剂策略。