核仁素
脂质体
基因沉默
适体
阳离子脂质体
黑色素瘤
癌症研究
分子生物学
转染
材料科学
生物
基因
细胞生物学
生物化学
纳米技术
细胞质
核仁
作者
Liyu Li,Jianjun Hou,XJ Liu,Yujia Guo,Yun Wu,Lihe Zhang,Zhenjun Yang
出处
期刊:Biomaterials
[Elsevier BV]
日期:2014-02-02
卷期号:35 (12): 3840-3850
被引量:283
标识
DOI:10.1016/j.biomaterials.2014.01.019
摘要
BRAF gene mutation is found in more than 60% of malignant melanomas, which are difficult to treat. In this study, a new tumor-targeting liposome was developed to deliver anti-BRAF siRNA (siBraf) for the treatment of melanomas. Nucleolin is overexpressed on the surface of cancer cells. AS1411, an aptamer showing specific binding to nucleolin, was conjugated to PEGylated cationic liposome as the targeting probe ASLP (AS1411-PEG-liposome). The ASLP/siRNA complex was formed through electrostatic interaction between ASLP and siRNA. The binding of AS1411 to the surface of PEGylated liposomes was confirmed by gel electrophoresis and capillary electrophoresis. Real-time PCR and Western blot analysis showed that ASLP/siBraf exhibited strong silencing activity of BRAF gene. The much higher accumulation of the siRNA in tumor cells comparing with normal cells indicated that ASLP displayed excellent tumor-targeting capability. Notably, ASLP/siBraf showed significant silencing activity in A375 tumor xenograft mice and inhibited the melanoma growth. These results suggested that the new nucleolin-targeted siRNA delivery system by AS1411 may have the potential for the treatment of melanoma.
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