Upgrade of an old drug: Auranofin in innovative cancer therapies to overcome drug resistance and to increase drug effectiveness

IF 10.9 1区 医学 Q1 CHEMISTRY, MEDICINAL
Tania Gamberi, Giovanni Chiappetta, Tania Fiaschi, Alessandra Modesti, Flavia Sorbi, Francesca Magherini
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引用次数: 28

Abstract

Auranofin is an oral gold(I) compound, initially developed for the treatment of rheumatoid arthritis. Currently, Auranofin is under investigation for oncological application within a drug repurposing plan due to the relevant antineoplastic activity observed both in vitro and in vivo tumor models. In this review, we analysed studies in which Auranofin was used as a single drug or in combination with other molecules to enhance their anticancer activity or to overcome chemoresistance. The analysis of different targets/pathways affected by this drug in different cancer types has allowed us to highlight several interesting targets and effects of Auranofin besides the already well-known inhibition of thioredoxin reductase. Among these targets, inhibitory-κB kinase, deubiquitinates, protein kinase C iota have been frequently suggested. To rationalize the effects of Auranofin by a system biology-like approach, we exploited transcriptomic data obtained from a wide range of cell models, extrapolating the data deposited in the Connectivity Maps website and we attempted to provide a general conclusion and discussed the major points that need further investigation.

一种老药的升级:在创新的癌症治疗中克服耐药性并提高药物有效性
金嘌呤是一种口服金(I)化合物,最初用于治疗类风湿性关节炎。目前,由于在体外和体内肿瘤模型中观察到相关的抗肿瘤活性,因此正在研究在药物再利用计划中的肿瘤应用。在这篇综述中,我们分析了auraurofin作为单一药物或与其他分子联合使用以增强其抗癌活性或克服化学耐药的研究。对该药物在不同癌症类型中影响的不同靶点/途径的分析,使我们能够强调除已知的硫氧还蛋白还原酶抑制作用外,金糠蛋白的几个有趣的靶点和作用。在这些靶点中,抑制-κB激酶、去泛素化酶、蛋白激酶C - iota被频繁提出。为了通过类似系统生物学的方法使Auranofin的作用合理化,我们利用了从广泛的细胞模型中获得的转录组学数据,推断了存储在Connectivity Maps网站上的数据,我们试图提供一个一般性结论,并讨论了需要进一步研究的要点。
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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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