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本文引用的文献

1
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。
J Cell Biochem. 2010 Jan 1;109(1):162-172. doi: 10.1002/jcb.22394.
2
Multinational, double-blind, phase III study of prednisone and either satraplatin or placebo in patients with castrate-refractory prostate cancer progressing after prior chemotherapy: the SPARC trial.多中心、双盲、III 期研究泼尼松与沙他膦或安慰剂联合治疗化疗后进展的去势抵抗性前列腺癌患者:SPARC 试验。
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3
Application of metal coordination chemistry to explore and manipulate cell biology.应用金属配位化学探索和操控细胞生物学。
Chem Rev. 2009 Oct;109(10):4921-60. doi: 10.1021/cr900134a.
4
Platinum drug distribution in cancer cells and tumors.铂类药物在癌细胞和肿瘤中的分布。
Chem Rev. 2009 Oct;109(10):4911-20. doi: 10.1021/cr9001066.
5
Medicinal inorganic chemistry approaches to passivation and removal of aberrant metal ions in disease.用于疾病中异常金属离子钝化和去除的药用无机化学方法。
Chem Rev. 2009 Oct;109(10):4885-910. doi: 10.1021/cr9000176.
6
Copper in diseases and treatments, and copper-based anticancer strategies.铜在疾病和治疗中的作用,以及基于铜的抗癌策略。
Med Res Rev. 2010 Jul;30(4):708-49. doi: 10.1002/med.20174.
7
Metals in anticancer therapy: copper(II) complexes as inhibitors of the 20S proteasome.金属在抗癌治疗中的作用:铜(II)配合物作为 20S 蛋白酶体的抑制剂。
Eur J Med Chem. 2009 Nov;44(11):4353-61. doi: 10.1016/j.ejmech.2009.05.019. Epub 2009 May 24.
8
The rational design of anticancer platinum complexes: the importance of the structure-activity relationship.抗癌铂配合物的合理设计:构效关系的重要性。
Curr Med Chem. 2009;16(18):2235-60. doi: 10.2174/092986709788453087.
9
Clinical development of novel proteasome inhibitors for cancer treatment.新型蛋白酶体抑制剂在癌症治疗中的临床开发。
Expert Opin Investig Drugs. 2009 Jul;18(7):957-71. doi: 10.1517/13543780903002074.
10
Comparative activities of nickel(II) and zinc(II) complexes of asymmetric [NN'O] ligands as 26S proteasome inhibitors.镍(II)和锌(II)配合物的不对称 [NN'O] 配体作为 26S 蛋白酶体抑制剂的比较活性。
Inorg Chem. 2009 Jul 6;48(13):5928-37. doi: 10.1021/ic900276g.

新型金属和金属配合物作为癌症治疗的平台。

Novel metals and metal complexes as platforms for cancer therapy.

机构信息

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

出版信息

Curr Pharm Des. 2010 Jun;16(16):1813-25. doi: 10.2174/138161210791209009.

DOI:10.2174/138161210791209009
PMID:20337575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3759287/
Abstract

Metals are essential cellular components selected by nature to function in several indispensable biochemical processes for living organisms. Metals are endowed with unique characteristics that include redox activity, variable coordination modes, and reactivity towards organic substrates. Due to their reactivity, metals are tightly regulated under normal conditions and aberrant metal ion concentrations are associated with various pathological disorders, including cancer. For these reasons, coordination complexes, either as drugs or prodrugs, become very attractive probes as potential anticancer agents. The use of metals and their salts for medicinal purposes, from iatrochemistry to modern day, has been present throughout human history. The discovery of cisplatin, cis-[Pt(II) (NH(3))(2)Cl(2)], was a defining moment which triggered the interest in platinum(II)- and other metal-containing complexes as potential novel anticancer drugs. Other interests in this field address concerns for uptake, toxicity, and resistance to metallodrugs. This review article highlights selected metals that have gained considerable interest in both the development and the treatment of cancer. For example, copper is enriched in various human cancer tissues and is a co-factor essential for tumor angiogenesis processes. However the use of copper-binding ligands to target tumor copper could provide a novel strategy for cancer selective treatment. The use of nonessential metals as probes to target molecular pathways as anticancer agents is also emphasized. Finally, based on the interface between molecular biology and bioinorganic chemistry the design of coordination complexes for cancer treatment is reviewed and design strategies and mechanisms of action are discussed.

摘要

金属是生物体中几种不可或缺的生化过程所必需的细胞成分,是大自然选择的。金属具有独特的特性,包括氧化还原活性、可变的配位方式和对有机底物的反应性。由于其反应性,金属在正常条件下受到严格调控,异常的金属离子浓度与各种病理紊乱有关,包括癌症。由于这些原因,配合物,无论是作为药物还是前药,都成为潜在抗癌剂的非常有吸引力的探针。从iatrochemistry 到现代,金属及其盐类一直被用于医学目的。顺铂,顺-[Pt(II)(NH(3))(2)Cl(2)]的发现是一个决定性的时刻,它引发了人们对铂(II)和其他含金属配合物作为潜在新型抗癌药物的兴趣。该领域的其他兴趣涉及对金属药物的摄取、毒性和耐药性的关注。本文重点介绍了在癌症的开发和治疗中引起广泛关注的几种金属。例如,铜在各种人类癌症组织中富集,是肿瘤血管生成过程所必需的辅助因子。然而,使用铜结合配体来靶向肿瘤铜可以为癌症的选择性治疗提供一种新的策略。非必需金属作为探针靶向分子途径作为抗癌剂的用途也得到了强调。最后,基于分子生物学和生物无机化学之间的界面,综述了用于癌症治疗的配合物的设计,并讨论了设计策略和作用机制。