肿瘤靶向基因转移与DNA多聚体。

Manfred Ogris, Ernst Wagner
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引用次数: 70

摘要

治疗应用需要系统的基因传递系统;在某些情况下,靶细胞可能遍布整个生物体,如癌症转移的情况,只能通过全身途径到达。在非病毒载体类别中,基于聚合物的转染颗粒(称为DNA多聚体)和基于脂质的系统(称为DNA脂质体)正在为此目的而开发。对于体循环,必须掩盖DNA复合物的表面电荷,以避免与血浆成分、红细胞和网状内皮系统相互作用。在其他载体配方中,基于聚乙烯亚胺(PEI),用聚乙二醇(PEG)屏蔽,并与受体结合配体转铁蛋白(Tf)或表皮生长因子(EGF)连接的多聚物已经开发出来。发现复合物以受体依赖和细胞周期依赖的方式介导有效的基因转移到肿瘤细胞系。将表面屏蔽的Tf-PEI复合物系统地注入小鼠尾静脉,导致基因优先传递到远处生长的皮下肿瘤。相反,带正电荷的PEI多聚体的应用主要将基因转移到肺部。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor-targeted gene transfer with DNA polyplexes.

Systemic gene delivery systems are needed for therapeutic applications; in some situations, target cells might be spread throughout the organism, as in the case of cancer metastases, which can be reached only via the systemic route. Within the class of nonviral vectors, polymer-based transfection particles named DNA polyplexes and lipid-based systems named DNA lipoplexes are being developed for this purpose. For systemic circulation, masking the surface charge of DNA complexes has to be accomplished to avoid interactions with plasma components, erythrocytes, and the reticuloendothelial system. Among other vector formulations, polyplexes based on polyethylenimine (PEI), shielded with polyethylene glycol (PEG), and linked to the receptor binding ligands transferrin (Tf) or epidermal growth factor (EGF) have been developed. Complexes were found to mediate efficient gene transfer into tumor cell lines in a receptor-dependent and cell-cycle-dependent manner. Systemic administration of surface-shielded Tf-PEI polyplexes into the tail vein of mice resulted in preferential gene delivery into distantly growing subcutaneous tumors. In contrast, application of positively charged PEI polyplexes directed gene transfer primarily to the lung.

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