Discovery of an acridine-based fluorescent ligand for selectively targeting mitochondrial G-quadruplexes DNA and triggering cervical cancer cell death
Mitochondrial G-quadruplexes (mtG4s) have recently emerged as a highly promising therapeutic target in oncology. This is because the frequency of their formation in the mitochondrial DNA (mtDNA) of cancer cells is significantly higher than that in normal cells. The stabilization of mtG4s induces instability in mtDNA, which subsequently triggering mitochondrial dysfunction and programmed cell death-a mechanistic paradigm that unveils novel avenues for cancer therapy. Despite promising prospects, the development of specific ligands targeting mtG4s remains a substantial unaddressed challenge. In this study, we designed and synthesized an acridine derivative, YWB-6. YWB-6 demonstrated remarkable mitochondrial targeting specificity and inherent fluorescence properties. Biophysical characterization confirmed that YWB-6 selectively recognizes and stabilizes mtG4 structures with high affinity. In SiHa cervical cancer cell models, YWB-6 exhibited precise binding to mtG4, leading to mitochondrial membrane integrity disruption, ATP depletion, ROS imbalance, and ultimately cell cycle arrest and apoptosis. Mechanistic investigations revealed that YWB-6 exerts its antitumor effects primarily through mtG4-mediated mitochondrial dysfunction. Cellular assays further verified its potent antitumor activity, with IC
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Funding
Key Research and Development Program of Ningxia Grant 2023BEG02012National Natural Science Foundation of China Grant 21867016National Natural Science Foundation of China Grant 82404405National Natural Science Foundation of China Grant 82360676Ministry of Education Grant KFKT202311Natural Science Foundation of Ningxia Province Grant 2024AAC03351Natural Science Foundation of Ningxia Province Grant 2024AAC03291Natural Science Foundation of Ningxia Province Grant 2023AAC03186Ningxia Medical University Grant XT2023025