核酸
化学
小RNA
细胞质
核仁素
细胞凋亡
DNA
细胞
癌细胞
药物输送
适体
程序性细胞死亡
细胞生物学
感应(电子)
肽核酸
基因传递
核糖核酸
癌症
分子生物学
生物化学
基因
遗传增强
生物
遗传学
物理化学
有机化学
核仁
作者
Pan Fu,Hao Chen,Lilin Ouyang,Lin Li,Yuhui Wang,Sihua Qian,Zhanglei Cao,Kerong Wu,Jie Chao,Jianping Zheng
标识
DOI:10.1021/acs.analchem.2c04760
摘要
Antisense peptide nucleic acid (asPNA), an effective antisense drug, has been employed as a gene therapy agent and a useful tool in molecular biology. Gaining control over the delivery of asPNA to target tissues has been a major hindrance to its wide application in clinical practice. A simple and efficient DNA nanoribbon (DNR)-based drug delivery process has been designed in this study that releases the asPNA agent to inhibit oncogenic microRNAs (miRNAs). Furthermore, we demonstrated how the AS1411 aptamer that binds nucleolin on the cell membranes works as a control mechanism capable of identifying target cancer cells and enhancing the enrichment capacity of DNR. With the biodegradability of DNR, we can efficiently initiate the release of asPNA into the cytoplasm, particularly targeting the intended miR-21 and synergistically increasing programmed cell death 4 (PDCD4) expression to enhance cell apoptosis. We assume that this well-defined delivery mechanism will aid in designing antisense site-specific treatments for various diseases, including cancer.
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