Medical School of Southeast University, Nanjing, Jiangsu, China.
Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, China.
Artif Cells Nanomed Biotechnol. 2020 Dec;48(1):116-128. doi: 10.1080/21691401.2019.1699817.
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.
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。