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设计并构建一种用于实体瘤栓塞治疗的磁靶向促凝蛋白。

Design and construction of a magnetic targeting pro-coagulant protein for embolic therapy of solid tumors.

机构信息

Medical School of Southeast University, Nanjing, Jiangsu, China.

Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, China.

出版信息

Artif Cells Nanomed Biotechnol. 2020 Dec;48(1):116-128. doi: 10.1080/21691401.2019.1699817.

DOI:10.1080/21691401.2019.1699817
PMID:31852257
Abstract

In this study, we have designed a magnetic targeting pro-coagulant protein (MTPCP) for the embolic therapy of solid tumours. The MTPCP consists of a magnetic carrier and a pro-coagulant protein. The pro-coagulant protein used in this study is the fusion protein tTF-EG3287 which is not pro-coagulant when free in the blood circulation, but presents strong pro-coagulant ability once bound to the Neuropilin-1(NRP-1) that is highly expressed on tumour-associated vascular endothelial cells. And the magnetic carrier is O-Carboxymethyl chitosan-coated iron oxide nanoparticles (OCMC/FeO). , we assessed the NRP-1 targeting ability of the MTPCP using confocal microscopy and flow cytometry, and evaluated the potential pro-coagulant activity of the MTPCP using the Spectozyme FXa assay. , the magnetic targeting ability of the MTPCP was detected using a living imaging system. At last, we assessed the anticancer activity of the MTPCP on HepG2 tumour bearing BALB/c nude mice models including subcutaneous transplantation and orthotopic transplantation. HepG2 tumour bearing mice models revealed that after intravenous administration of the MTPCP, thrombosis specifically occurs on tumour-associated blood vessels, and resulting in tumour growth retardation. No apparent side effects, such as thrombosis in other organs or other treatment-related toxicity, were observed during the treatment. Our data showed that the MTPCP may be a promising embolic agent for the embolic therapy of solid tumours.

摘要

在这项研究中,我们设计了一种用于实体瘤栓塞治疗的磁靶向促凝血蛋白(MTPCP)。MTPCP 由磁性载体和促凝血蛋白组成。本研究中使用的促凝血蛋白是融合蛋白 tTF-EG3287,它在血液循环中自由时没有促凝血作用,但一旦与高度表达于肿瘤相关血管内皮细胞上的 Neuropilin-1(NRP-1)结合,就呈现出很强的促凝血能力。而磁性载体是 O-羧甲基壳聚糖包覆的氧化铁纳米颗粒(OCMC/FeO)。 我们使用共聚焦显微镜和流式细胞术评估了 MTPCP 的 NRP-1 靶向能力,并使用 Spectozyme FXa 测定法评估了 MTPCP 的潜在促凝血活性。 我们使用活体成像系统检测了 MTPCP 的磁靶向能力。最后,我们在 HepG2 肿瘤荷瘤 BALB/c 裸鼠模型中评估了 MTPCP 的抗癌活性,包括皮下移植和原位移植。HepG2 肿瘤荷瘤小鼠模型显示,静脉注射 MTPCP 后,肿瘤相关血管特异性发生血栓形成,导致肿瘤生长迟缓。在治疗过程中未观察到明显的副作用,如其他器官的血栓形成或其他与治疗相关的毒性。我们的数据表明,MTPCP 可能是一种有前途的用于实体瘤栓塞治疗的栓塞剂。

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