紫杉醇
适体
胶质母细胞瘤
核酸
血脑屏障
材料科学
纳米技术
DNA
化学
癌症研究
生物医学工程
医学
化疗
生物化学
分子生物学
内科学
生物
中枢神经系统
作者
Sirong Shi,Wei Fu,Shiyu Lin,Taoran Tian,Songhang Li,Xiaoru Shao,Yuxin Zhang,Tao Zhang,Zisheng Tang,Yi Zhou,Yunfeng Lin,Xiaoxiao Cai
标识
DOI:10.1016/j.nano.2019.102061
摘要
Targeted DNA nanoparticles have been identified as one of the most promising nanocarriers in anti-glioma drug delivery. We established a multifunctional nanosystem for targeted glioma therapy. Tetrahedral framework nucleic acid (tFNA), entering U87MG cells and bEnd.3 cells, was chosen to deliver two aptamers, GMT8 and Gint4.T, and paclitaxel. GMT8 and Gint4.T, which specifically bind with U87MG cells and with PDGFRβ, were linked with tFNA, to form Gint4.T-tFNA-GMT8 (GTG). GTG was efficiently internalized by U87MG and bEnd.3 cells and penetrated an in-vitro blood-brain-barrier model. GTG loaded with paclitaxel (GPC) had potentiated anti-glioma efficacy. It inhibited the proliferation, migration, and invasion of U87MG cells, and enhanced apoptosis induction in these cells. The expression of apoptosis-related proteins was significantly changed after treatment with GPC, confirming apoptosis induction. Our study demonstrated that the combination of GTG and paclitaxel has great potential for glioma treatment and tFNA shows great promise for use in drug delivery.
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