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PEG10 antisense oligonucleotide is an experimental RNA-targeted therapeutic designed to selectively inhibit the expression of Paternally Expressed Gene 10 (PEG10). PEG10 is a retrotransposon-derived protein that is typically silenced in adult tissues but frequently reactivated in various malignancies, including neuroendocrine-like muscle-invasive bladder cancer (MIBC), hepatocellular carcinoma, and neuroendocrine prostate cancer. The ASO functions by binding to PEG10 mRNA, which triggers its degradation and subsequently reduces PEG10 protein levels. Preclinical research indicates that silencing PEG10 can resensitize cancer cells to chemotherapy, induce cell cycle arrest by increasing p21 and p27 levels, and decrease the expression of epithelial-mesenchymal transition (EMT) markers such as SLUG and SNAIL, thereby inhibiting tumor growth, invasion, and metastasis.
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