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旧的金属结合药物在人类癌症治疗中的新应用。

New applications of old metal-binding drugs in the treatment of human cancer.

作者信息

Schmitt Sara M, Frezza Michael, Dou Qing Ping

机构信息

Barbara Ann Karmanos Cancer Institute, School of Medicine, Wayne State University, Detroit, Michigan 48201, USA.

出版信息

Front Biosci (Schol Ed). 2012 Jan 1;4(1):375-91. doi: 10.2741/274.

DOI:10.2741/274
PMID:22202066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3646510/
Abstract

Significant advances in the use of metal complexes, precipitated by platinum, have fostered a renewed interest in harnessing their rich potential in the treatment of cancer. In addition to platinum-based complexes, the anticancer properties of other metals such as ruthenium have been realized, and ruthenium-based compounds are currently being investigated in clinical trials. Since the process of drug development can be expensive and cumbersome, finding new applications of existing drugs may provide effective means to expedite the regulatory process in bringing new drugs to the clinical setting. Encouraging findings from laboratory studies reveal significant anticancer activity from different classes of metal-chelating compounds, such as disulfiram, clioquinol, and dithiocarbamate derivatives that are currently approved for the treatment of various pathological disorders. Their use as coordination complexes with metals such as copper, zinc, and gold that target the ubiquitin-proteasome pathway have shown significant promise as potential anticancer agents. This review discusses the unique role of several selected metals in relation to their anti-cancer properties as well as the new therapeutic potential of several previously approved metal-chelating drugs. In vitro and in vivo experimental evidence along with mechanisms of action (e.g., via targeting the tumor proteasome) will also be discussed with anticipation of strengthening this exciting new concept.

摘要

由铂引发的金属配合物使用方面的重大进展,激发了人们对利用其在癌症治疗中丰富潜力的新兴趣。除了铂基配合物外,其他金属如钌的抗癌特性也已被认识到,基于钌的化合物目前正在临床试验中进行研究。由于药物开发过程可能昂贵且繁琐,寻找现有药物的新应用可能为加快新药进入临床环境的监管过程提供有效手段。实验室研究的令人鼓舞的结果表明,不同类别的金属螯合化合物具有显著的抗癌活性,例如目前已被批准用于治疗各种病理疾病的双硫仑、氯碘羟喹和二硫代氨基甲酸盐衍生物。它们作为与铜、锌和金等金属的配位配合物,靶向泛素 - 蛋白酶体途径,已显示出作为潜在抗癌剂的巨大前景。本综述讨论了几种选定金属在抗癌特性方面的独特作用,以及几种先前批准的金属螯合药物的新治疗潜力。还将讨论体外和体内实验证据以及作用机制(例如,通过靶向肿瘤蛋白酶体),以期加强这一令人兴奋的新概念。

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本文引用的文献

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Inhibition of tumor proteasome activity by gold-dithiocarbamato complexes via both redox-dependent and -independent processes.金-二硫代氨基甲酸盐复合物通过氧化还原依赖和非依赖两种过程抑制肿瘤蛋白酶体活性。
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Overview of Antabuse (Disulfiram) in Radiation and Cancer Biology.戒酒硫(双硫仑)在放射与癌症生物学中的概述
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Metal-based proteasomal deubiquitinase inhibitors as potential anticancer agents.基于金属的蛋白酶体去泛素化酶抑制剂作为潜在的抗癌药物。
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