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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Vinorelbine cationic liposomes modified with wheat germ agglutinin for inhibiting tumor metastasis in treatment of brain glioma
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Vinorelbine cationic liposomes modified with wheat germ agglutinin for inhibiting tumor metastasis in treatment of brain glioma

机译:用小麦胚芽凝集素修饰的血肠氨酸阳离子脂质体,用于抑制肿瘤转移治疗脑胶质瘤

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Glioma is the most common primary malignant brain tumor with a poor prognosis. The application of chemotherapeutic drugs is limited due to the existence of blood-brain barrier and serious side effects. Liposomes have been proven to be a stable and useful drug delivery system for tumors. In this paper, WGA (wheat germ agglutinin) modified vinorelbine cationic liposomes had been successfully constructed for treating glioma. In the liposomes, WGA was modified on the liposomal surface for crossing the blood-brain barrier and increasing the targeting effects, 3-(N-(N, N-dimethylaminoethane) carbamoyl) cholesterol (DC-Chol) was used as cationic material and vinorelbine was encapsulated in the aqueous core of liposomes to inhibit tumor metastasis and kill tumor cells. Studies were performed on C6 cells in vitro and were verified in brain glioma-bearing mice in vivo. Results in vitro demonstrated that the targeting liposomes could induce C6 cells apoptosis, promote drugs across the blood-brain barrier, inhibit the metastasis of tumor cells and increase targeting effects to tumor cells. Meanwhile, action mechanism studies showed that the targeting liposomes could down-regulate PI3K, MMP-2, MMP-9 and FAK to inhibit tumor metastasis. Results in vivo exhibited that the targeting liposomes displayed an obvious antitumor efficacy by accumulating selectively in tumor site and exhibited low toxicity to blood system and major organs. Hence, WGA modified vinorelbine cationic liposomes might provide a safe and efficient therapy strategy for glioma.
机译:胶质瘤是最常见的原发性恶性脑肿瘤,预后差。化学治疗药物的应用受到血脑屏障存在的有限和严重的副作用。已被证明脂质体是肿瘤的稳定和有用的药物递送系统。本文已成功构建WGA(小麦胚芽凝集素)改性的血岭阳离子脂质体用于治疗胶质瘤。在脂质体中,在脂质体表面上修饰WGA,用于穿过血脑屏障并增加靶向效果,使用3-(N-(N-二甲基氨基氨基甲烷)碳酰烷基)胆固醇(DC-CHOL)作为阳离子材料和血肠籽包封在脂质体的含水核中以抑制肿瘤转移并杀死肿瘤细胞。在体外对C6细胞进行研究,在体内患有脑胶质瘤小鼠的核实。结果体外证明靶向脂质体可诱导C6细胞凋亡,促进血脑屏障的药物,抑制肿瘤细胞的转移,并将靶向效应增加对肿瘤细胞。同时,动作机制研究表明,靶向脂质体可以下调PI3K,MMP-2,MMP-9和FAK以抑制肿瘤转移。体内的结果表明,靶向脂质体通过在肿瘤部位中的选择性积累并表现出对血液系统和主要器官的低毒性而显示出明显的抗肿瘤效果。因此,WGA改性的血岭突阳离子脂质体可以为胶质瘤提供安全有效的治疗策略。

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