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Endogenously Activated Multiple DNAzyme-Encoded Nanoflowers for High-Contrast Imaging of Long Noncoding RNA and Cancer Therapy

脱氧核酶 热空气 核酸酶 核糖核酸 生存素 细胞生物学 癌症 纳米技术 内吞作用 长非编码RNA 分子信标 癌症治疗 细胞内 癌细胞 化学 纳米器件 肿瘤微环境 劈开 PARP1 效应器 生物物理学 癌症研究 DNA 适体 生物 光热治疗 血红素 内化 生物传感器 p14arf公司 小RNA 内生 细胞 细胞凋亡
作者
Huimin Yuan,Zichen Jiao,Tao Wang,Chun‐yang Zhang
出处
期刊:ACS Nano [American Chemical Society]
卷期号:19 (41): 36397-36410 被引量:8
标识
DOI:10.1021/acsnano.5c10251
摘要

Long noncoding RNAs (lncRNAs) are implicated in various physiological and pathological processes with the potential as diagnostic biomarkers and therapeutic targets. Watson–Crick base pairing-based DNA nanomaterials have been developed previously for diagnosis-guided therapy, but they are limited by undesired signal leakage and uncontrollable drug release due to nonspecific activation and nuclease susceptibility. Rolling circle amplification (RCA) products can noncanonically self-assemble into compact DNA nanoflowers with high loading performance and excellent nuclease resistance, but they are scarcely explored for intracellular analysis due to inefficient integration/release/activation of probes. Herein, we design endogenous acid-activatable ZnO-encapsulated RCA nanoflowers encoded by DNA-cleaving DNAzyme (D-DNAzyme) and RNA-cleaving DNAzyme (R-DNAzyme) for high-contrast imaging of lncRNA and controlled cancer therapy in living cells and mice. Upon the endocytosis of ZnO-RCA nanoflowers into the cells, the acidic microenvironment of tumor cells stimulates the decomposition of ZnO into Zn2+ that serves as DNAzyme cofactor and therapeutic reactive oxygen species producer. Zn2+-motivated D-DNAzyme-catalyzed detachment of RCA nanoflowers releases the deactivated R-DNAzyme. In the presence of lncRNA, the activity of R-DNAzyme is restored to cleave Cy5-labeled substrate probes on the AuNP surface with high turnover rate and specifically knocks down survivin gene, resulting in the generation of an enhanced fluorescence signal and R-DNAzyme-mediated gene silencing. Notably, the intrinsic resistance to nucleases and acid-stimulated detachment of RCA nanoflowers dramatically reduce the background signal leakage and improve the imaging contrast. This nanoplatform can accurately measure HOTAIR in living cells, real-time monitor HOTAIR in mice, and distinguish HOTAIR levels in healthy and cancerous breast tissues.
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