在神经母细胞瘤临床前模型中靶向 LGR5 的吡咯并二氮杂卓抗体-药物共轭物的抗肿瘤活性

Jianghua Tu, Yukimatsu Toh, Adela M. Aldana, Jake J. Wen, Ling Wu, J. Jacob, Li Li, Sheng Pan, Kendra S. Carmon, Qingyun J. Liu
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引用次数: 0

摘要

神经母细胞瘤(NB)是一种常见于 15 岁以下儿童的周围神经系统癌症。它是婴儿期最常见的癌症,占儿童癌症相关死亡总数的 12%。富亮氨酸重复含 G 蛋白偶联受体 5(LGR5)是一种膜受体,与胃肠道系统癌症的原发肿瘤形成和转移有关。值得注意的是,在 NB 肿瘤细胞中发现了高水平的 LGR5,而 LGR5 的高表达与生存率低密切相关。抗体药物共轭物(ADC)是一种单克隆抗体,它与杀死细胞的细胞毒素共价连接,将有效载荷送入癌细胞。我们采用化学酶联方法生成了一种含有抗 LGR5 抗体和吡咯并二氮卓(PBD)二聚体有效载荷 SG3199 的 ADC。所制备的抗 LGR5 ADC 能够抑制表达 LGR5 的 NB 细胞的生长,且具有很高的效力和特异性。重要的是,该 ADC 能够以 PBD 类 ADC 的临床相关剂量完全抑制体内 NB 异种移植肿瘤的生长。这些研究结果支持了利用PBD类有效载荷靶向LGR5治疗高风险NB的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antitumor Activity of a Pyrrolobenzodiazepine Antibody–Drug Conjugate Targeting LGR5 in Preclinical Models of Neuroblastoma
Neuroblastoma (NB) is a cancer of the peripheral nervous system found in children under 15 years of age. It is the most frequently diagnosed cancer during infancy, accounting for ~12% of all cancer-related deaths in children. Leucine-rich repeat-containing G-protein-coupled receptor 5 (LGR5) is a membrane receptor that is associated with the primary tumor formation and metastasis of cancers in the gastrointestinal system. Remarkably, high levels of LGR5 are found in NB tumor cells, and high LGR5 expression is strongly correlated with poor survival. Antibody–drug conjugates (ADCs) are monoclonal antibodies that are covalently linked to cell-killing cytotoxins to deliver the payloads into cancer cells. We generated an ADC with an anti-LGR5 antibody and pyrrolobenzodiazepine (PBD) dimer-based payload SG3199 using a chemoenzymatic conjugation method. The resulting anti-LGR5 ADC was able to inhibit the growth of NB cells expressing LGR5 with high potency and specificity. Importantly, the ADC was able to completely inhibit the growth of NB xenograft tumors in vivo at a clinically relevant dose for the PBD class of ADCs. The findings support the potential of targeting LGR5 using the PBD class of payload for the treatment of high-risk NBs.
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