Aura Biosciences, Cambridge, Massachusetts.
Emory Eye Center, Emory University, Atlanta, Georgia.
Mol Cancer Ther. 2018 Feb;17(2):565-574. doi: 10.1158/1535-7163.MCT-17-0953. Epub 2017 Dec 14.
The work outlined herein describes AU-011, a novel recombinant papillomavirus-like particle (VLP) drug conjugate and its initial evaluation as a potential treatment for primary uveal melanoma. The VLP is conjugated with a phthalocyanine photosensitizer, IRDye 700DX, that exerts its cytotoxic effect through photoactivation with a near-infrared laser. We assessed the anticancer properties of AU-011 utilizing a panel of human cancer cell lines and using murine subcutaneous and rabbit orthotopic xenograft models of uveal melanoma. The specificity of VLP binding (tumor targeting), mediated through cell surface heparan sulfate proteoglycans (HSPG), was assessed using HSPG-deficient cells and by inclusion of heparin in studies. Our results provide evidence of potent and selective anticancer activity, both and AU-011 activity was blocked by inhibiting its association with HSPG using heparin and using cells lacking surface HSPG, indicating that the tumor tropism of the VLP was not affected by dye conjugation and cell association is critical for AU-011-mediated cytotoxicity. Using the uveal melanoma xenograft models, we observed tumor uptake following intravenous (murine) and intravitreal (rabbit) administration and, after photoactivation, potent dose-dependent tumor responses. Furthermore, in the rabbit orthotopic model, which closely models uveal melanoma as it presents in the clinic, tumor treatment spared the retina and adjacent ocular structures. Our results support further clinical development of this novel therapeutic modality that might transform visual outcomes and provide a targeted therapy for the early-stage treatment of patients with this rare and life-threatening disease. .
本文概述了 AU-011 的研究,这是一种新型的重组乳头瘤病毒样颗粒(VLP)药物偶联物,最初被评估为治疗原发性眼葡萄膜黑色素瘤的潜在药物。该 VLP 与酞菁类光敏剂 IRDye 700DX 相连,通过近红外激光的光激活发挥其细胞毒性作用。我们利用一系列人类癌细胞系评估了 AU-011 的抗癌特性,并利用小鼠皮下和兔原位异种移植模型评估了眼葡萄膜黑色素瘤。通过使用缺乏 HSPG 的细胞和在研究中包含肝素,评估了 VLP 结合(肿瘤靶向)的特异性,该结合是通过细胞表面硫酸乙酰肝素蛋白聚糖(HSPG)介导的。我们的结果提供了有力的证据,证明 AU-011 具有强大的选择性抗癌活性,AU-011 的活性均被抑制其与 HSPG 结合的肝素和缺乏表面 HSPG 的细胞所阻断,这表明 VLP 的肿瘤趋向性不受染料偶联的影响,细胞结合对于 AU-011 介导的细胞毒性至关重要。使用眼葡萄膜黑色素瘤异种移植模型,我们观察到静脉内(小鼠)和玻璃体内(兔)给药后的肿瘤摄取,并且在光激活后,观察到了强大的、剂量依赖性的肿瘤反应。此外,在兔原位模型中,该模型与临床中葡萄膜黑色素瘤的表现非常相似,肿瘤治疗使视网膜和相邻的眼部结构免受影响。我们的研究结果支持进一步开发这种新型治疗方法,这种方法可能会改变视觉结果,并为这种罕见的、危及生命的疾病的早期治疗提供一种靶向治疗方法。