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揭示过渡金属配合物在医学中的潜力:从实验室到体内应用的基于金属药物的转化原位激活。

Unveiling the Potential of Transition Metal Complexes for Medicine: Translational in Situ Activation of Metal-Based Drugs from Bench to in Vivo Applications.

机构信息

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences Laboratory for Inorganic Chemical Biology, FR-75005, Paris, France.

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisboa, Portugal.

出版信息

Chembiochem. 2021 May 14;22(10):1740-1742. doi: 10.1002/cbic.202100015. Epub 2021 Feb 25.

DOI:10.1002/cbic.202100015
PMID:33507625
Abstract

The development of metal-based anticancer drugs has been hampered, among other reasons, by their lack of selectivity for cancer cells. In a recent article, Zou and co-workers presented the successful intracellular activation of organogold(I) complexes for potential cancer treatment through Pd(II)-mediated transmetallation, overcoming some off-target activity of novel gold-based drugs. This unique strategy builds the perfect bridge between metallodrug usage and bioorthogonal intracellular catalysis for more advanced and selective therapies. Such an approach will hopefully pave the way for forthcoming studies in medicinal inorganic chemistry.

摘要

金属抗癌药物的发展受到多种因素的阻碍,其中包括它们对癌细胞缺乏选择性。在最近的一篇文章中,邹等人通过钯(II)介导的转金属化成功地实现了有机金(I)配合物在细胞内的激活,从而克服了新型金基药物的一些脱靶活性,为潜在的癌症治疗提供了可能。这种独特的策略在金属药物的使用和生物正交的细胞内催化之间架起了完美的桥梁,为更先进和更具选择性的治疗方法奠定了基础。这种方法有望为医学无机化学的未来研究铺平道路。

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