4.8 Article

A One-Two-Three Multifunctional System for Enhanced Imaging and Detection of Intracellular MicroRNA and Chemogene Therapy

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 24, 页码 27825-27835

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c04353

关键词

fluorescence; surface-enhanced Raman scattering (SERS); miR-21; dual-mode DNA robot (DDR) probe; therapy

资金

  1. Natural Science Foundation of China [21775081]
  2. Shandong Provincial Key Research and Development Program [2019GSF107024]
  3. Key Laboratory Open Fund [SATM201602]

向作者/读者索取更多资源

The study introduces a novel "one-two-three" system for enhanced imaging and detection of miRNA-21 in cancer cells, as well as chemogene therapy. The system features a miR-21-triggered endogenous substance-accelerated cyclic reaction, two signal switch modes, and three functions including enhanced imaging, detection, and comprehensive treatment.
Simultaneous imaging, diagnosis, and therapy can offer an effective strategy for cancer treatment. However, the complex probe design, poor drug release efficiency, and multidrug resistance remain tremendous challenges to cancer treatment. Here, a novel one-two-three system is built for enhanced imaging and detection of miRNA-21 (miR-21) overexpressed in cancer cell and chemogene therapy. The system consists of dual-mode DNA robot nanoprobes assembled by two types of hairpin DNAs and three-way branch DNAs modified on gold nanoparticles, with intercalating anticancer drugs (doxorubicin), into DNA duplex GC base pairs. In the system, via intracellular ATP-accelerated cyclic reaction triggered by miR-21, fluorescence and SERS signals were alternated with DNA structure switch, and the precise SERS detection of miRNA and fluorescence imaging oriented on-demand release of two types of anticancer drugs (anti-miR-21 and Dox) are achieved. Thus, one-two-three means one kind of miR-21-triggered endogenous substance accelerated cyclic reaction, two modes of signal switch, and three functions including enhanced imaging, detection, and comprehensive treatment. The one-two-three system has some notable merits. First, ATP as an endogenous substance promotes DNA structure switching and accelerates the cyclic reaction. Second, the treatment with a dual-mode signal switch is more reliable and accurate and can provide more abundant information than a single-mode treatment platform. Thus, the imaging and detection of intracellular miRNA and effective comprehensive therapy are realized. In vivo results indicate that the system can provide new insights and strategies for diagnosis and therapy.

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