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A Novel AKR1C3 Specific Prodrug TH3424 With Potent Antitumor Activity in Liver Cancer.

作者信息

He Ping, Wang Chunnian, Wang Yanlan, Wang Caiyan, Zhou Changhua, Cao Donglin, Li Jiang, Bushnell David A, Li Qing, Kornberg Roger D, Xie Wei, Wang Zhong

机构信息

School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, China.

Centre for Cellular & Structural Biology, Sun Yat-Sen University, Guangzhou, China.

出版信息

Clin Pharmacol Ther. 2021 Jul;110(1):229-237. doi: 10.1002/cpt.2171. Epub 2021 Mar 10.

Abstract

Overexpression of AKR1C3, an aldo-keto reductase, was recently discovered in liver cancers. In this study, an inverse correlation between AKR1C3 expression and survival of patients with liver cancer was observed. AKR1C3 inhibitors, however, failed to suppress liver cancer cell growth. The prodrug TH3424, which releases a DNA alkylating reagent upon reduction by AKR1C3, was developed to target tumors with overexpression of AKR1C3. TH3424 showed specific killing of liver cancer cells with AKR1C3 overexpression both in vitro and in vivo. In patient-derived mouse xenograft models, TH3424 at doses as low as 1.5 mg/kg eliminated liver tumors with no apparent toxicity. Therefore, TH3424 is a promising drug candidate for liver cancer and other types of cancers overexpressing AKR1C3.

摘要

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