Molecular Science and Biomedicine Laboratory, College of Biology and College of Chemistry and Chemical Engineering, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University, Changsha 410082, China.
Proc Natl Acad Sci U S A. 2013 May 14;110(20):7998-8003. doi: 10.1073/pnas.1220817110. Epub 2013 Apr 29.
Nanotechnology has allowed the construction of various nanostructures for applications, including biomedicine. However, a simple target-specific, economical, and biocompatible drug delivery platform with high maximum tolerated doses is still in demand. Here, we report aptamer-tethered DNA nanotrains (aptNTrs) as carriers for targeted drug transport in cancer therapy. Long aptNTrs were self-assembled from only two short DNA upon initiation by modified aptamers, which worked like locomotives guiding nanotrains toward target cancer cells. Meanwhile, tandem "boxcars" served as carriers with high payload capacity of drugs that were transported to target cells and induced selective cytotoxicity. aptNTrs enhanced maximum tolerated dose in nontarget cells. Potent antitumor efficacy and reduced side effects of drugs delivered by biocompatible aptNTrs were demonstrated in a mouse xenograft tumor model. Moreover, fluorophores on nanotrains and drug fluorescence dequenching upon release allowed intracellular signaling of nanotrains and drugs. These results make aptNTrs a promising targeted drug transport platform for cancer theranostics.
纳米技术允许构建各种用于应用的纳米结构,包括生物医学。然而,人们仍然需要一种简单的、靶向特异性、经济实惠且生物相容的药物输送平台,其具有高最大耐受剂量。在这里,我们报告了适体连接的 DNA 纳米列车(aptNTrs)作为癌症治疗中靶向药物输送的载体。长 aptNTrs 仅由两个短 DNA 在经过修饰的适体启动后自组装而成,这些适体像火车头一样引导纳米列车驶向靶癌细胞。同时,串联的“货车”作为载体,具有高载药量,可将药物运输到靶细胞并诱导选择性细胞毒性。aptNTrs 在非靶细胞中增加了最大耐受剂量。在小鼠异种移植肿瘤模型中,证明了生物相容的 aptNTrs 递送的药物具有强大的抗肿瘤功效和降低的副作用。此外,纳米列车上的荧光团和药物荧光猝灭释放后允许纳米列车和药物的细胞内信号传导。这些结果使 aptNTrs 成为癌症治疗学中一种有前途的靶向药物输送平台。