Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy

被引:41
作者
Li, Ling [1 ,2 ,3 ]
Li, Xia [1 ,2 ,3 ]
Wu, Yuzhe [4 ]
Song, Linjiang [1 ,2 ,3 ]
Yang, Xi [1 ,2 ,3 ]
He, Tao [1 ,2 ,3 ]
Wang, Ning [1 ,2 ,3 ]
Yang, Suleixin [1 ,2 ,3 ]
Zeng, Yan [1 ,2 ,3 ]
Wu, Qinjie [1 ,2 ,3 ]
Qian, Zhiyong [1 ,2 ,3 ]
Wei, Yuquan [1 ,2 ,3 ]
Gong, Changyang [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Ctr Canc, Chengdu 610041, Peoples R China
[3] Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Peoples R China
[4] Xiamen Univ, Coll Mat, Xiamen 361005, Peoples R China
关键词
gene delivery; nuclear targeting; hyaluronic acid; TRAIL; cancer stem cells; colon cancer; CANCER STEM-CELLS; POLYMERIC NANOPARTICLES; VIRAL VECTORS; BREAST-CANCER; DELIVERY; APOPTOSIS; CARRIER; DENDRIMERS; EFFICACY; FLUORINE;
D O I
10.7150/thno.17588
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cancer stem cell-like cells (CSCL) are responsible for tumor recurrence associated with conventional therapy (e.g. surgery, radiation, and chemotherapy). Here, we developed a novel multifunctional nucleus-targeting nanoparticle-based gene delivery system which is capable of targeting and eradicating CSCL. These nanoparticles can facilitate efficient endosomal escape and spontaneously penetrate into nucleus without additional nuclear localization signal. They also induced extremely high gene transfection efficiency (>95%) even in culture medium containing 30% serum, which significantly surpassed that of some commercial transfection reagents, such as Lipofectamine 2000 and Lipofectamine 3000 etc. Especially, when loaded with the TRAIL gene, this system mediated remarkable depletion of CSCL. Upon systemic administration, the nanoparticles accumulated in tumor sites while sparing the non-cancer tissues and significantly inhibited the growth of tumors with no evident systemic toxicity. Taken together, our results suggest that these novel multifunctional, nucleus-targeting nanoparticles are a very promising in vivo gene delivery system capable of targeting CSCL and represent a new treatment candidate for improving the survival of cancer patients.
引用
收藏
页码:1633 / 1649
页数:17
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