Enzon Pharmaceuticals, Piscataway, NJ 08854, USA.
Angiogenesis. 2011 Sep;14(3):245-53. doi: 10.1007/s10456-011-9209-1. Epub 2011 Mar 31.
Topoisomerase I inhibitors down-regulate HIF-1α leading to tumor growth inhibition, but only while maintaining sustained levels of drug exposure. EZN-2208, a multi-arm 40 kDa pegylated, releasable SN38-drug conjugate, provides higher, longer lasting exposure of tumors to SN38 in contrast to SN38 that is released from CPT-11. EZN-2208 also consistently has greater antitumor activity than CPT-11 in a variety of solid and hematological tumor models. In this report, the ability of PEG-SN38 to down-regulate HIF-1α and its downstream targets, in a more potent, sustained manner compared with CPT-11 was examined. To do so, U251 glioma xenografts that stably expressed a hypoxia response element-dependent luciferase reporter gene were implanted in mice. After treatment it was found that EZN-2208 induced potent, sustained HIF-1α down-regulation (37% at 48 h and 83% at 120 h) in the tumors, whereas CPT-11 caused only minor, transient HIF-1α down-regulation. In addition, EZN-2208 down-regulated mRNA levels of HIF-1α targeted genes (MMP2, VEGF1, Glut1, Glut3 and TGFβ1). Further, western blot analyses of xenograft tumors demonstrated that EZN-2208 had significantly more effect than CPT-11 in down-regulating HIF-1α, VEGF, Glut1 and MMP2 protein levels. Significant down-regulation of HIF-1α and VEGF proteins translated to EZN-2208's superior anti-angiogenic activity compared with CPT-11, confirmed by microvessel density reduction in a chorioallantoic membrane assay and in CD-31 immunohistochemistry studies. Additional studies done with matrigel implants devoid of tumor cells show that EZN-2208 significantly inhibits angiogenesis while CPT-11 has little or no effect. It is concluded that the superior antitumor activity of EZN-2208 compared with CPT-11 is attributed, in part, to an anti-angiogenic effect. Ongoing clinical Phase I and Phase II studies will assess safety and efficacy of EZN-2208.
拓扑异构酶 I 抑制剂下调 HIF-1α 导致肿瘤生长抑制,但只有在持续维持药物暴露水平的情况下才会如此。EZN-2208 是一种多臂 40 kDa 聚乙二醇化、可释放的 SN38 药物偶联物,与从 CPT-11 释放的 SN38 相比,它能为肿瘤提供更高、更持久的 SN38 暴露。与 CPT-11 相比,EZN-2208 在各种实体瘤和血液系统肿瘤模型中始终具有更强的抗肿瘤活性。在本报告中,研究了 PEG-SN38 以比 CPT-11 更有效、更持久的方式下调 HIF-1α 及其下游靶标的能力。为此,将稳定表达缺氧反应元件依赖性荧光素酶报告基因的 U251 神经胶质瘤异种移植到小鼠中。结果发现,EZN-2208 在肿瘤中诱导强烈、持续的 HIF-1α 下调(48 小时时为 37%,120 小时时为 83%),而 CPT-11 仅引起轻微、短暂的 HIF-1α 下调。此外,EZN-2208 下调了 HIF-1α 靶向基因(MMP2、VEGF1、Glut1、Glut3 和 TGFβ1)的 mRNA 水平。进一步的异种移植肿瘤 Western blot 分析表明,EZN-2208 下调 HIF-1α、VEGF、Glut1 和 MMP2 蛋白水平的效果明显优于 CPT-11。在鸡胚绒毛尿囊膜试验和 CD-31 免疫组化研究中,HIF-1α 和 VEGF 蛋白的显著下调证实了 EZN-2208 优于 CPT-11 的抗血管生成活性。在没有肿瘤细胞的 Matrigel 植入物中进行的其他研究表明,EZN-2208 可显著抑制血管生成,而 CPT-11 几乎没有或没有影响。结论是,与 CPT-11 相比,EZN-2208 的优越抗肿瘤活性部分归因于抗血管生成作用。正在进行的 I 期和 II 期临床研究将评估 EZN-2208 的安全性和疗效。