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]
日期:2025-10-09
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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