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癌症分子生物学与设计细胞毒性金(I)和金(III)配合物的策略:教程综述。

Cancer molecular biology and strategies for the design of cytotoxic gold(I) and gold(III) complexes: a tutorial review.

机构信息

Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Johannesburg 2050, South Africa.

Laboratory of Inorganic Chemistry, Environmental and Chemical Engineering, University of Oulu, P. O. Box 3000, 90014 Oulu, Finland.

出版信息

Dalton Trans. 2021 Dec 7;50(47):17413-17437. doi: 10.1039/d1dt02783b.

Abstract

This tutorial review highlights key principles underpinning the design of selected metallodrugs to target specific biological macromolecules (DNA and proteins). The review commences with a descriptive overview of the eukaryotic cell cycle and the molecular biology of cancer, particularly apoptosis, which is provided as a necessary foundation for the discovery, design, and targeting of metal-based anticancer agents. Drugs which target DNA have been highlighted and clinically approved metallodrugs discussed. A brief history of the development of mainly gold-based metallodrugs is presented prior to addressing ligand systems for stabilizing and adding functionality to bio-active gold(I) and gold(III) complexes, particularly in the burgeoning field of anticancer metallodrugs. Concepts such as multi-modal and selective cytotoxic agents are covered where necessary for selected compounds. The emerging role of carbenes as the ligand system of choice to achieve these goals for gold-based metallodrug candidates is highlighted prior to closing the review with comments on some future directions that this research field might follow. The latter section ultimately emphasizes the importance of understanding the fate of metal complexes in cells to garner key mechanistic insights.

摘要

本教程综述重点介绍了设计针对特定生物大分子(DNA 和蛋白质)的金属药物的关键原则。本综述首先对真核细胞周期和癌症的分子生物学,特别是细胞凋亡进行了描述性概述,这为发现、设计和靶向基于金属的抗癌药物提供了必要的基础。重点介绍了靶向 DNA 的药物,并讨论了临床批准的金属药物。在讨论稳定和赋予生物活性金(I)和金(III)配合物功能的配体系统之前,简要介绍了主要基于金的金属药物的发展历史,特别是在新兴的抗癌金属药物领域。对于选定的化合物,在必要时涵盖了多模式和选择性细胞毒性剂等概念。强调了卡宾作为配体系统的新兴作用,以实现基于金的金属药物候选物的这些目标,然后在评论一些未来可能的研究方向后结束综述。最后一部分强调了了解金属配合物在细胞中的命运以获得关键机制见解的重要性。

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