Exogenous and Endogenous Dual-Activated Nanoladder for Precise Imaging of Mitochondrial Ferroptosis-Related Inhibition miRNA with Tumor Cell Specificity

Developing precise tumor cell-specific mitochondrial ferroptosis-related inhibition miRNA imaging methods holds enormous potential for anticancer drug screening and cancer treatment. Nevertheless, traditional amplification methods still tolerated the limited tumor specificity because of the “off-tum...

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Veröffentlicht in:Analytical chemistry (Washington) 2024-05, Vol.96 (19), p.7550-7557
Hauptverfasser: Yin, Yue, Chen, Shuwei, Li, Haiming, Pang, Xiaozhe, Wang, Congkai, Wang, Lei, Liu, Pingping, Xu, Shenghao, Luo, Xiliang
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Sprache:eng
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Zusammenfassung:Developing precise tumor cell-specific mitochondrial ferroptosis-related inhibition miRNA imaging methods holds enormous potential for anticancer drug screening and cancer treatment. Nevertheless, traditional amplification methods still tolerated the limited tumor specificity because of the “off-tumor” signal leakage resulting from their “always-active” sensing mode. To overcome this limitation, we herein developed a dual (exogenous 808 nm NIR light and endogenous APE1) activated nanoladder for precise imaging of mitochondrial ferroptosis-related miRNA with tumor cell specificity and improved imaging resolution. Exogenous NIR light-activation can regulate the ferroptosis-related inhibition miRNA imaging signals within mitochondria, and endogenous enzyme-activation can confine signals to tumor cells. Based on this dual activation design, off-tumor signals were greatly reduced and tumor-to-background contrast was enhanced with an improved tumor/normal discrimination ratio, realizing tumor cell-specific precise imaging of mitochondrial ferroptosis-related inhibition miRNA.
ISSN:0003-2700
1520-6882
1520-6882
DOI:10.1021/acs.analchem.4c00332