ArticleMolecular therapy. Nucleic acids2026
Aptamer-guided delivery of miR-126 suppresses glioblastoma stem-like cell invasion and tumor progression.
Article in Molecular therapy. Nucleic acids, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Glioblastoma, IDH-wildtype (GBM) is the most common and aggressive primary brain tumor in adults, with a median overall survival of 15-18 months. New therapeutic targets are needed to improve patients' prognosis. Due to their powerful regulatory capabilities, miRNAs could be possible candidate targets. MiR-126 is considered a tumor suppressor in several cancers, including GBM. In a previous study, we found that the infiltrative shift observed in response to bevacizumab in a GBM mouse model, induced a high miR-126 downregulation, confirming its tumor-suppressor function, exerted by inhibiting growth and angiogenesis. Here, we either stably restored miR-126 expression in GBM stem-like cells by transduction or transiently delivered it through an A40s aptamer-based conjugate. Both interventions led to an overall impairment of tumorigenic properties. Notably,
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