Drug Discovery Division, Southern Research Institute, Birmingham, AL, United States.
Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, OH, United States.
Cancer Lett. 2014 Jul 10;349(1):8-14. doi: 10.1016/j.canlet.2014.04.003. Epub 2014 Apr 13.
The rapid development of new anticancer drugs that are safe and effective is a common goal shared by basic scientists, clinicians and patients. The current review discusses one such agent, namely niclosamide, which has been used in the clinic for the treatment of intestinal parasite infections. Recent studies repeatedly identified niclosamide as a potential anticancer agent by various high-throughput screening campaigns. Niclosamide not only inhibits the Wnt/β-catenin, mTORC1, STAT3, NF-κB and Notch signaling pathways, but also targets mitochondria in cancer cells to induce cell cycle arrest, growth inhibition and apoptosis. A number of studies have established the anticancer activities of niclosamide in both in vitro and in vivo models. Moreover, the inhibitory effects of niclosamide on cancer stem cells provide further evidence for its consideration as a promising drug for cancer therapy. This article reviews various aspects of niclosamide as they relate to its efficacy against cancer and associated molecular mechanisms.
新型安全有效的抗癌药物的快速发展是基础科学家、临床医生和患者的共同目标。本文讨论了一种这样的药物,即氯硝柳胺,它已在临床上用于治疗肠道寄生虫感染。最近的研究通过各种高通量筛选活动反复将氯硝柳胺鉴定为一种潜在的抗癌药物。氯硝柳胺不仅抑制 Wnt/β-catenin、mTORC1、STAT3、NF-κB 和 Notch 信号通路,还靶向癌细胞中的线粒体,诱导细胞周期停滞、生长抑制和细胞凋亡。许多研究已经在体外和体内模型中证实了氯硝柳胺的抗癌活性。此外,氯硝柳胺对癌症干细胞的抑制作用为其作为癌症治疗有前途的药物提供了进一步的证据。本文综述了氯硝柳胺在其抗癌功效及其相关分子机制方面的各个方面。