Li Jin, Qiu Liping, Xie Sitao, Zhang Jing, Zhang Liqin, Liu Honglin, Li Juan, Zhang Xiaobing, Tan Weihong
Molecular Science and Biomedicine Laboratory, State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, College of Life Sciences, Aptamer Engineering Center of Hunan Province, Hunan University, Hunan 410082, China.
Center for Research at Bio/Nano Interface, Department of Chemistry and Department of Physiology and Functional Genomics, Health Cancer Center, UF Genetics Institute and McKnight Brain Institute, University of Florida, Gainesville, Florida 32611-7200, USA.
Sci China Chem. 2018 Apr;61(4):497-504. doi: 10.1007/s11426-017-9176-3. Epub 2018 Jan 11.
Drug administration customized to individual cells could intrinsically address cancer heterogeneity and provide a safe and effective method for delivering personalized treatment. To accomplish this, we developed a smart nanodrug delivery system characterized by cancer cell-targeted drug delivery and intracellular biomarker-responsive drug activation. This system was composed of a long-nicked DNA duplex formed by tandem hybridization of two extended antisense oligonucleotides whose ends were separately blocked with a cancer cell-specific aptamer, AS1411, and a replaceable anti-biomarker probe (ABP). We demonstrated that this DNA nanodrug was directed to cancer cells with the guidance power of AS1411 and then activated by the presence of a given intracellular biomarker. By using such a belt-and-braces strategy, this DNA nanodrug system could safely and efficiently accelerate apoptosis of target cancer cells. Moreover, since the expression level of biomarkers tends to indicate the specific physiological state of individual cells, biomarker-responsive activation of the nanodrug is expected to enable customized drug administration at the cellular level.
针对个体细胞定制的药物给药方式本质上可以解决癌症异质性问题,并为提供个性化治疗提供一种安全有效的方法。为实现这一目标,我们开发了一种智能纳米药物递送系统,其特点是癌细胞靶向药物递送和细胞内生物标志物响应性药物激活。该系统由一个长切口的DNA双链体组成,该双链体由两个延伸的反义寡核苷酸串联杂交形成,其末端分别用癌细胞特异性适配体AS1411和可替换的抗生物标志物探针(ABP)封闭。我们证明,这种DNA纳米药物在AS1411的引导作用下被导向癌细胞,然后在特定细胞内生物标志物存在的情况下被激活。通过使用这种双保险策略,这种DNA纳米药物系统可以安全有效地加速靶癌细胞的凋亡。此外,由于生物标志物的表达水平往往表明个体细胞的特定生理状态,因此纳米药物的生物标志物响应性激活有望在细胞水平实现定制化药物给药。