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MC1 is a small molecule photosensitizer that selectively targets the RNA G-quadruplex (RG4) structure located in the 5'-untranslated region (5'-UTR) of KRAS mRNA. Developed as a more selective and safer alternative to the ligand MBD, MC1 facilitates photodynamic therapy (PDT) by inducing KRAS RG4 breakage, depleting glutathione (GSH), and oxidizing NADH upon light activation. These actions trigger ferroptosis in cancer cells, particularly in cisplatin-resistant non-small cell lung cancer (NSCLC). Additionally, MC1 serves as a fluorescent probe for the detection and characterization of KRAS RG4.
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