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ST-3 is a small molecule inhibitor of the RNA-binding protein HuR (ELAV-like protein 1), identified and characterized by researchers at the University of Kansas Medical Center. HuR is a key regulator that stabilizes mRNAs associated with tumor progression, metastasis, and chemoresistance. ST-3 works by directly binding to HuR and disrupting its interaction with target mRNAs, such as Snail, thereby inhibiting epithelial-mesenchymal transition (EMT) and the maintenance of cancer stem cells (CSCs). In preclinical models of pancreatic cancer, ST-3 has shown efficacy in reducing cell migration, invasion, and spheroid formation, particularly in cell lines with high HuR expression.
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