Lin Chi-Kang, Bai Meng-Yi, Hu Teh-Min, Wang Yu-Chi, Chao Tai-Kuang, Weng Shao-Ju, Huang Rui-Lan, Su Po-Hsuan, Lai Hung-Cheng
Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.
Department of Obstetrics and Gynecology, Tri-Service General Hospital, Taipei, Taiwan.
Oncotarget. 2016 Feb 23;7(8):8993-9006. doi: 10.18632/oncotarget.7113.
Ovarian cancer treatment remains a challenge and targeting cancer stem cells presents a promising strategy. Niclosamide is an "old" antihelminthic drug that uncouples mitochondria of intestinal parasites. Although recent studies demonstrated that niclosamide could be a potential anticancer agent, its poor water solubility needs to be overcome before further preclinical and clinical investigations can be conducted. Therefore, we evaluated a novel nanosuspension of niclosamide (nano-NI) for its effect against ovarian cancer. Nano-NI effectively inhibited the growth of ovarian cancer cells in which it induced a metabolic shift to glycolysis at a concentration of less than 3 μM in vitro and suppressed tumor growth without obvious toxicity at an oral dose of 100 mg/kg in vivo. In a pharmacokinetic study after oral administration, nano-NI showed rapid absorption (reaching the maximum plasma concentration within 5 min) and improved the bioavailability (the estimated bioavailability for oral nano-NI was 25%). In conclusion, nano-NI has the potential to be a new treatment modality for ovarian cancer and, therefore, further clinical trials are warranted.
卵巢癌治疗仍然是一项挑战,而靶向癌症干细胞是一种有前景的策略。氯硝柳胺是一种“老”的抗蠕虫药物,可使肠道寄生虫的线粒体解偶联。尽管最近的研究表明氯硝柳胺可能是一种潜在的抗癌药物,但在进行进一步的临床前和临床研究之前,其水溶性差的问题需要克服。因此,我们评估了一种新型氯硝柳胺纳米混悬液(nano-NI)对卵巢癌的作用。Nano-NI在体外有效抑制卵巢癌细胞的生长,在浓度低于3μM时诱导其代谢转变为糖酵解,在体内口服剂量为100mg/kg时抑制肿瘤生长且无明显毒性。在口服给药后的药代动力学研究中,nano-NI显示出快速吸收(在5分钟内达到最大血浆浓度)并提高了生物利用度(口服nano-NI的估计生物利用度为25%)。总之,nano-NI有潜力成为卵巢癌的一种新治疗方式,因此有必要进行进一步的临床试验。