Entin-Meer Michal, Rephaeli Ada, Yang Xiaodong, Nudelman Abraham, Nudelman Ayelet, Haas-Kogan Daphne Adele
Department of Radiation Oncology, Neurological Surgery, and Comprehensive Cancer Center, University of California, San Francisco, CA 94143, USA.
Cancer Lett. 2007 Aug 18;253(2):205-14. doi: 10.1016/j.canlet.2007.01.022. Epub 2007 Mar 7.
Butyroyloxymethyl-4-phenylbutyrate (AN-113) is a novel HDACI that releases potent anti-neoplastic derivatives upon intracellular hydrolysis. The precursor of AN-113, 4-phenylbutyrate has shown promising results in a Phase I study of gliomas, and we hypothesized that AN-113 offers significant advantages over the parent drug. AN-113 demonstrates selective in vitro cytotoxicity against malignant cells while sparing normal astrocytes, effective at doses over 20-fold lower than 4-phenylbutyrate. Combining AN-113 and radiation results in additive therapeutic effects. Enthusiasm is lent to this approach by the ability of AN-113 to efficiently kill glioma cells, its bioavailability and potency when administered orally, its capacity to cross the blood-brain barrier, and its effectiveness in combination with radiation.
丁酰氧基甲基-4-苯基丁酸酯(AN-113)是一种新型组蛋白去乙酰化酶抑制剂,在细胞内水解后会释放出强效抗肿瘤衍生物。AN-113的前体4-苯基丁酸在一项针对胶质瘤的I期研究中已显示出有前景的结果,并且我们推测AN-113比母体药物具有显著优势。AN-113在体外对恶性细胞表现出选择性细胞毒性,同时对正常星形胶质细胞无损害,其有效剂量比4-苯基丁酸低20多倍。将AN-113与放疗联合可产生相加的治疗效果。AN-113有效杀死胶质瘤细胞的能力、口服给药时的生物利用度和效力、穿过血脑屏障的能力以及与放疗联合的有效性,都为这种方法带来了希望。