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miRNA-6883 lipid nanoparticles are an experimental RNA-based therapeutic consisting of microRNA 6883-5p (miR-6883) encapsulated within a lipid nanoparticle (LNP) delivery system. Developed by SMURF Therapeutics in collaboration with Brown University, the drug functions by silencing the expression of cyclin-dependent kinases 4 and 6 (CDK4/6). This inhibition triggers the degradation of Hypoxia-Inducible Factor 1α (HIF1α) via the E3 ubiquitin ligase SMURF2, effectively targeting both cell cycle progression and hypoxia-driven survival pathways in cancer cells. Preclinical data presented at AACR 2026 demonstrated significant anti-tumor activity in colorectal and breast cancer models, particularly when combined with MEK inhibitors or ferroptosis-inducing agents.
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