Pan Jing-Xuan, Ding Ke, Wang Cheng-Yan
Department of Pathophysiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong 510089, PR China.
Chin J Cancer. 2012 Apr;31(4):178-84. doi: 10.5732/cjc.011.10290. Epub 2012 Jan 9.
Niclosamide, an oral antihelminthic drug, has been used to treat tapeworm infection for about 50 years. Niclosamide is also used as a molluscicide for water treatment in schistosomiasis control programs. Recently, several groups have independently discovered that niclosamide is also active against cancer cells, but its precise mechanism of antitumor action is not fully understood. Evidence supports that niclosamide targets multiple signaling pathways (NF-κB, Wnt/β-catenin, Notch, ROS, mTORC1, and Stat3), most of which are closely involved with cancer stem cells. The exciting advances in elucidating the antitumor activity and the molecular targets of this drug will be discussed. A method for synthesizing a phosphate pro-drug of niclosamide is provided. Given its potential antitumor activity, clinical trials for niclosamide and its derivatives are warranted for cancer treatment.
氯硝柳胺是一种口服抗蠕虫药物,已用于治疗绦虫感染约50年。氯硝柳胺还用作血吸虫病控制项目中水处理的杀螺剂。最近,几个研究小组独立发现氯硝柳胺对癌细胞也有活性,但其抗肿瘤作用的确切机制尚未完全了解。有证据表明氯硝柳胺靶向多种信号通路(NF-κB、Wnt/β-连环蛋白、Notch、ROS、mTORC1和Stat3),其中大多数与癌症干细胞密切相关。将讨论在阐明该药物的抗肿瘤活性和分子靶点方面取得的令人兴奋的进展。提供了一种合成氯硝柳胺磷酸前药的方法。鉴于其潜在的抗肿瘤活性,有必要对氯硝柳胺及其衍生物进行癌症治疗的临床试验。