a Hongqiao International Institute of Medicine, Shanghai Tongren Hospital and Faculty of Public Health , Shanghai Jiao Tong University School of Medicine , Shanghai , China.
b Department of Comparative Biosciences and the Molecular and Environmental Toxicology Center , University of Wisconsin-Madison , Madison , WI , USA.
Expert Opin Drug Discov. 2018 Sep;13(9):815-824. doi: 10.1080/17460441.2018.1508207. Epub 2018 Aug 13.
6-Mercaptopurine (6-MP) and 6-thioguanine (6-TG), two anticancer drugs, have high systemic toxicity due to a lack of target specificity. Therefore, increasing target selectivity should improve drug safety. Areas covered: The authors examined the hypothesis that new prodrug designs based upon mechanisms of kidney-selective toxicity of trichloroethylene would reduce systemic toxicity and improve selectivity to kidney and tumor cells. Two approaches specifically were investigated. The first approach was based upon bioactivation of trichloroethylene-cysteine S-conjugate by renal cysteine S-conjugate β-lyases. The prodrugs obtained were kidney-selective but exhibited low turnover rates. The second approach was based on the toxic mechanism of trichloroethylene-cysteine S-conjugate sulfoxide, a Michael acceptor that undergoes rapid addition-elimination reactions with biological thiols. Expert opinion: Glutathione-dependent Michael addition-elimination reactions appear to be an excellent strategy to design highly efficient anticancer drugs. Targeting glutathione could be a promising approach for the development of anticancer prodrugs because cancer cells usually upregulate glutathione biosynthesis and/or glutathione S-transferases expression.
6-巯基嘌呤(6-MP)和 6-硫鸟嘌呤(6-TG)是两种抗癌药物,由于缺乏靶向特异性,具有很高的全身毒性。因此,提高靶向选择性应该可以提高药物安全性。
作者研究了以下假设:基于三氯乙烯对肾脏选择性毒性的机制设计新的前药设计可以降低全身毒性并提高对肾脏和肿瘤细胞的选择性。具体研究了两种方法。第一种方法基于三氯乙烯-半胱氨酸 S-结合物由肾脏半胱氨酸 S-结合物β-裂解酶的生物活化。获得的前药具有肾脏选择性,但转化率低。第二种方法基于三氯乙烯-半胱氨酸 S-结合物亚砜的毒性机制,亚砜是一种迈克尔受体,与生物硫醇发生快速加成-消除反应。
谷胱甘肽依赖性迈克尔加成-消除反应似乎是设计高效抗癌药物的绝佳策略。靶向谷胱甘肽可能是开发抗癌前药的有前途的方法,因为癌细胞通常上调谷胱甘肽生物合成和/或谷胱甘肽 S-转移酶的表达。