Nanotherapy Targeting miR-10b Improves Survival in Orthotopic Glioblastoma Models
Recommended Citation
Kim B, Chen M, Mondal S, Kenyon E, Mallett C, de Carvalho AC, Medarova Z, Moore A. Nanotherapy Targeting miR-10b Improves Survival in Orthotopic Glioblastoma Models. J Funct Biomater 2025; 17(1).
Document Type
Article
Publication Date
12-26-2025
Publication Title
J Funct Biomater
Keywords
glioblastoma; image-guided therapy; miRNA; nanoparticle
Abstract
Glioblastoma (GBM) is the most aggressive primary cancer with poor survival. In the absence of an effective treatment and a high probability of recurrence, new therapeutic approaches are urgently needed. This study focused on targeting microRNA-10b (miR-10b) highly expressed in GBM cells that has been identified as one of the key drivers of GBM progression. Inhibiting miR-10b using antisense oligonucleotides (ASOs) has shown promise, but its delivery is challenging due to short circulation half-life, degradation by nucleases, and limited blood-brain barrier (BBB) permeability. To overcome these barriers, we employed a magnetic nanoparticle (MN) platform to deliver anti-miR-10b ASOs (MN-anti-miR10b). In addition to serving as a delivery vehicle, these nanoparticles can be used for monitoring delivery using magnetic resonance imaging (MRI). In therapeutic studies in orthotopic models of GBM presented here we used MN-anti-miR10b as well as TTX-MC138, a clinically tested anti-miR10b nanotherapeutic now in Phase I trials in patients with solid (non-GBM) cancers. Both formulations showed efficient delivery, as demonstrated by imaging and improved survival, leading to target inhibition and increased apoptosis. This approach may offer a novel strategy for delivering therapeutics to GBM and improving patient outcomes in one of the most aggressive and treatment-resistant forms of brain cancer.
PubMed ID
41590784
Volume
17
Issue
1
