光动力疗法
光子上转换
生存素
脱氧核酶
癌症研究
材料科学
纳米器件
癌细胞
癌症
DNA
纳米技术
化学
生物
光电子学
发光
生物化学
有机化学
遗传学
作者
Yi Jin,Hao Wang,Xiaona Li,Han Zhu,Danna Sun,Xiaojing Sun,Huifang Liu,Ziying Zhang,Lingzhi Cao,Changlin Gao,Hui Wang,Xing‐Jie Liang,Jinchao Zhang,Xinjian Yang
标识
DOI:10.1021/acsami.0c03274
摘要
Although considerable clinical attempts on various kinds of cancers have been made, photodynamic therapy (PDT) still suffers from attenuated therapeutic effects because of the developed resistance of cancer cells. As a novel antiapoptosis protein, survivin has been demonstrated to be selectively overexpressed in a great number of human malignancies and plays a significant part in cancer progression and therapeutic resistance. Herein, we present an upconversion nanoplatform for enhanced PDT by DNAzyme-mediated gene silencing of survivin. In our system, a long single-stranded DNA (ssDNA) with a repetitive aptamer (AS1411) and survivin-targeted DNAzyme was fabricated by rolling circle amplification (RCA) and adsorbed on the upconversion nanoparticles (UCNPs) by electrostatic attraction. The multivalence of the ssDNA endows the upconversion nanoplatform with high recognition and loading capacity of photosensitizers and DNAzymes. When the nanoplatform is targeted internalized into cancer cells, PDT can be triggered by near-infrared (NIR) light to generate reactive oxygen species (ROS) for killing the cancer cells. Moreover, the encoded DNAzyme can efficiently inhibit the gene expression of survivin, providing the potential to enhance the efficiency of PDT. This study thus highlights the promise of an upconversion photodynamic nanoplatform for admirable combination therapy in cancer.
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