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用于实体瘤靶向治疗的膜联蛋白导向β-葡萄糖醛酸酶

Annexin-directed β-glucuronidase for the targeted treatment of solid tumors.

作者信息

Guillen Katrin P, Ruben Eliza A, Virani Needa, Harrison Roger G

机构信息

Biomedical Engineering Program and School of Chemical, Biological and Materials Engineering, University of Oklahoma, 100 E. Boyd St., Norman, OK 73019, USA.

Protein Production Core, Department of Chemistry and Biochemistry, University of Oklahoma, 101 Stephenson Parkway, Norman, OK 73019, USA.

出版信息

Protein Eng Des Sel. 2017 Feb;30(2):85-94. doi: 10.1093/protein/gzw063. Epub 2016 Dec 15.

Abstract

Enzyme prodrug therapy has the potential to remedy the lack of selectivity associated with the systemic administration of chemotherapy. However, most current systems are immunogenic and constrained to a monotherapeutic approach. We developed a new class of fusion proteins centered about the human enzyme β-glucuronidase (βG), capable of converting several innocuous prodrugs into chemotherapeutics. We targeted βG to phosphatidylserine on tumor cells, tumor vasculature and metastases via annexin A1/A5. Phosphatidylserine shows promise as a universal marker for solid tumors and allows for tumor type-independent targeting. To create fusion proteins, human annexin A1/A5 was genetically fused to the activity-enhancing 16a3 mutant of human βG, expressed in chemically defined, fed-batch suspension culture, and chromatographically purified. All fusion constructs achieved >95% purity with yields up to 740 μg/l. Fusion proteins displayed cancer selective cell-surface binding with cell line-dependent binding stability. One fusion protein in combination with the prodrug SN-38 glucuronide was as effective as the drug SN-38 on Panc-1 pancreatic cancer cells and HAAE-1 endothelial cells, and demonstrated efficacy against MCF-7 breast cancer cells. βG fusion proteins effectively enable localized combination therapy that can be tailored to each patient via prodrug selection, with promising clinical potential based on their near fully human design.

摘要

酶前药疗法有潜力弥补与全身化疗给药相关的选择性不足问题。然而,目前大多数系统具有免疫原性且局限于单一治疗方法。我们开发了一类以人β-葡萄糖醛酸酶(βG)为核心的新型融合蛋白,它能够将多种无害前药转化为化疗药物。我们通过膜联蛋白A1/A5将βG靶向肿瘤细胞、肿瘤血管和转移灶上的磷脂酰丝氨酸。磷脂酰丝氨酸有望成为实体瘤的通用标志物,并实现不依赖肿瘤类型的靶向。为了构建融合蛋白,将人膜联蛋白A1/A5与活性增强的人βG 16a3突变体进行基因融合,在化学成分明确的补料分批悬浮培养中表达,并通过色谱法纯化。所有融合构建体的纯度均超过95%,产量高达740μg/l。融合蛋白表现出癌症选择性细胞表面结合以及细胞系依赖性结合稳定性。一种融合蛋白与前药SN-38葡萄糖醛酸结合对Panc-1胰腺癌细胞和HAAE-1内皮细胞的效果与药物SN-38相同,并对MCF-7乳腺癌细胞显示出疗效。βG融合蛋白有效地实现了局部联合治疗,可通过前药选择为每位患者量身定制,基于其近乎完全人源化的设计具有广阔的临床应用潜力。

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