纳米探针
癌症生物标志物
细胞内
癌细胞
化学
纳米技术
小RNA
亚细胞定位
分子成像
胶体金
癌症
荧光寿命成像显微镜
生物物理学
癌症研究
细胞生物学
荧光
材料科学
细胞质
生物化学
纳米颗粒
生物
基因
物理
生物技术
量子力学
体内
遗传学
作者
Jian Lv,Shuai Chang,Hua‐Ying Chen,Xinyue Zhou,Xiaoyuan Wang,Zhen-Chi Chen,Binbin Chen,Ruo‐Can Qian,Da‐Wei Li
标识
DOI:10.1016/j.bios.2023.115325
摘要
The abnormal change in the expression profile of multiple cancer biomarkers is closely related to tumor progression and therapeutic effect. Due to their low abundance in living cells and the limitations of existing imaging techniques, simultaneous imaging of multiple cancer biomarkers has remained a significant challenge. Here, we proposed a multi-modal imaging strategy to detect the correlated expression of multiple cancer biomarkers, MUC1, microRNA-21 (miRNA-21) and reactive oxygen (ROS) in living cells, based on a porous covalent organic framework (COF) wrapped gold nanoparticles (AuNPs) core-shell nanoprobe. The nanoprobe is functionalized with Cy5-labeled MUC1 aptamer, a ROS-responsive molecule (2-MHQ), and a miRNA-21-response hairpin DNA tagged by FITC as the reporters for different biomarkers. The target-specific recognition can induce the orthogonal molecular change of these reporters, producing fluorescence and Raman signals for imaging the expression profiles of membrane MUC1 (red fluorescence channel), intracellular miRNA-21 (green fluorescence channel), and intracellular ROS (SERS channel). We further demonstrate the capability of the cooperative expression of these biomarkers, along with the activation of NF-κB pathway. Our research provides a robust platform for imaging multiple cancer biomarkers, with broad potential applications in cancer clinical diagnosis and drug discovery.
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