蛋白质组学方法在理解金属基抗癌药物作用机制中的应用。

Ying Wang, Jen-Fu Chiu
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引用次数: 35

摘要

抗癌药物顺铂的成功在很大程度上刺激了无机药物化学的发展。各种金属配合物目前被用作治疗剂(例如,铂、金和钌),用于治疗恶性疾病,包括几种类型的癌症。了解这些金属基药物的作用机制是为了设计更有效的药物。蛋白质组学方法与其他生化方法相结合,可以全面了解金属基抗癌药物诱导细胞死亡的反应,包括金属基抗癌药物的细胞毒性作用,蛋白质改变与药物靶点的相关性,以及耐药性和毒性的预测。这些信息与临床数据相结合,可以为未来设计和修改现有的金属基抗癌药物提供合理的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomic approaches in understanding action mechanisms of metal-based anticancer drugs.

Medicinal inorganic chemistry has been stimulating largely by the success of the anticancer drug, cisplatin. Various metal complexes are currently used as therapeutic agents (e.g., Pt, Au, and Ru) in the treatment of malignant diseases, including several types of cancers. Understanding the mechanism of action of these metal-based drugs is for the design of more effective drugs. Proteomic approaches combined with other biochemical methods can provide comprehensive understanding of responses that are involved in metal-based anticancer drugs-induced cell death, including insights into cytotoxic effects of metal-based anticancer drugs, correlation of protein alterations to drug targets, and prediction of drug resistance and toxicity. This information, when coupled with clinical data, can provide rational basses for the future design and modification of present used metal-based anticancer drugs.

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