顺铂
前药
药物输送
体内
癌细胞
癌症研究
生物相容性
内化
药品
癌症
DNA
材料科学
化学
纳米技术
药理学
化疗
细胞
医学
生物
生物化学
内科学
遗传学
有机化学
作者
Yi‐Fang Zhong,Jin Cheng,Yan Liu,Tao Luo,Yuqi Wang,Kai Jiang,Fangli Mo,Jie Song
出处
期刊:Small
[Wiley]
日期:2020-08-19
卷期号:16 (38)
被引量:33
标识
DOI:10.1002/smll.202003646
摘要
Abstract Cisplatin is a first‐line drug in clinical cancer treatment but its efficacy is often hindered by chemoresistance in cancer cells. Reduced intracellular drug accumulation is revealed to be a major mechanism of cisplatin resistance. Nanoscale drug delivery systems could help to overcome this problem because of their more active cellular uptake and more accurate tumor localization. DNA nanostructures have emerged as promising drug delivery systems because of their intrinsic biocompatibility and structural programmability. Herein, three diverse DNA nanostructures are constructed and their potential for cisplatin prodrug delivery is investigated. Results found that these DNA nanostructures could remarkably enhance the cellular internalization of platinum drugs and thus increase the anticancer activity, not only to regular lung cancer cells (A549), but more importantly to cisplatin‐resistant cancer cells (A549cisR). Further, in vivo studies also demonstrate that cisplatin prodrug loaded DNA nanostructures could effectively suppress tumor growth in both regular and cisplatin‐resistant tumor models. This study suggests that DNA nanostructures are effective carriers for platinum prodrug delivery to combat chemoresistance.
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