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EC1456 叶酸-微管蛋白抑制剂抗癌治疗药物的临床前评价

Pre-clinical evaluation of EC1456, a folate-tubulysin anti-cancer therapeutic.

机构信息

Endocyte, Inc., 3000 Kent Ave., Suite A1-100, West Lafayette, IN, 47906, USA.

出版信息

Sci Rep. 2018 Jun 12;8(1):8943. doi: 10.1038/s41598-018-27320-5.

Abstract

EC1456 is a folate-tubulysin conjugate constructed with an all-D enantiomeric spacer/linker configuration. When tested against folate receptor (FR)-positive cells, EC1456 demonstrated dose-responsive activity with an approximate 1000-fold level of specificity. Treatment of nude mice bearing FR-positive human xenografts (as large as 800 mm) with non-toxic doses of EC1456 led to cures in 100% of the mice. Combinations of low dose EC1456 with standard of care agents such as platins, taxanes, topotecan and bevacizumab, safely and significantly augmented the growth inhibitory effects of these commonly used agents. When tested against FR-positive human tumor xenograft models having confirmed resistance to a folate-vinca alkaloid (vintafolide), cisplatin or paclitaxel, EC1456 was found to generate partial to curative responses. Taken together, these studies demonstrate that EC1456 has significant anti-proliferative activity against FR-positive tumors, including models which were anticancer drug resistant, thereby justifying a Phase 1 trial of this agent for the treatment of advanced human cancers.

摘要

EC1456 是一种叶酸-微管蛋白偶联物,采用全 D 对映异构体间隔基/连接子构型构建。在针对叶酸受体(FR)阳性细胞的测试中,EC1456 表现出剂量依赖性活性,具有约 1000 倍的特异性。用非毒性剂量的 EC1456 治疗携带 FR 阳性人异种移植物(高达 800mm)的裸鼠导致 100%的小鼠治愈。低剂量 EC1456 与顺铂、紫杉烷、拓扑替康和贝伐单抗等标准治疗药物联合使用,可安全且显著增强这些常用药物的生长抑制作用。当在对叶酸-长春碱(vintafolide)、顺铂或紫杉醇有确认耐药性的 FR 阳性人肿瘤异种移植模型中进行测试时,发现 EC1456 可产生部分至治愈反应。综上所述,这些研究表明,EC1456 对 FR 阳性肿瘤具有显著的抗增殖活性,包括对抗癌药物耐药的模型,因此该药物有理由进行治疗晚期人类癌症的 1 期临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc1/5997627/d6eadc246471/41598_2018_27320_Fig1_HTML.jpg

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