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具有超高基因转染效率的多功能核靶向纳米颗粒用于基因治疗

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

作者信息

Li Ling, Li Xia, Wu Yuzhe, Song Linjiang, Yang Xi, He Tao, Wang Ning, Yang Suleixin, Zeng Yan, Wu Qinjie, Qian Zhiyong, Wei Yuquan, Gong Changyang

机构信息

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu, 610041, P. R. China.

College of Materials, Xiamen University, Xiamen 361005, P.R. China.

出版信息

Theranostics. 2017 Apr 10;7(6):1633-1649. doi: 10.7150/thno.17588. eCollection 2017.

Abstract

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 gene delivery system capable of targeting CSCL and represent a new treatment candidate for improving the survival of cancer patients.

摘要

癌症干细胞样细胞(CSCL)与传统疗法(如手术、放疗和化疗)相关的肿瘤复发有关。在此,我们开发了一种新型的基于多功能核靶向纳米颗粒的基因递送系统,该系统能够靶向并根除CSCL。这些纳米颗粒可促进高效的内体逃逸,并能在没有额外核定位信号的情况下自发穿透进入细胞核。它们甚至在含有30%血清的培养基中也能诱导极高的基因转染效率(>95%),这显著超过了一些商业转染试剂,如Lipofectamine 2000和Lipofectamine 3000等。特别地,当装载TRAIL基因时,该系统介导了CSCL的显著减少。经全身给药后,纳米颗粒在肿瘤部位积累,同时避免了非癌组织,并且显著抑制了肿瘤生长,没有明显的全身毒性。综上所述,我们的结果表明,这些新型的多功能核靶向纳米颗粒是一种非常有前景的能够靶向CSCL的基因递送系统,代表了一种改善癌症患者生存率的新的治疗候选方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4df2/5436517/66d907de5a5b/thnov07p1633g001.jpg

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