This research demonstrates tumor suppression in glioblastoma with peptide radiosensitizers, highlighting potential for improved radiotherapy.
Glioblastoma (GBM) radiotherapy is hampered by intrinsic radioresistance. Current radiosensitizers face two unresolved hurdles: inability to dynamically traverse sequential physiological barriers of GBM and lack of multitargeted action against the pathways driving radioresistance. Here, we developed h-Pep-MTZ, a biobarrier-adaptive peptide-radiosensitizer addressing both. This system undergoes smart multistage transformations to overcome key delivery barriers: It first circulates as large, negatively charged nanoparticles to prolong plasma half-life; then converts to small, positively charged particles via tumor-overexpressed heparanase for deep tumor penetration; and finally assembles into long nanofibers triggered by lysosomal cathepsin B and acidity to extend tumor retention. Importantly, the nanofibers mechanically disrupt lysosomes, increasing lysosomal membrane permeability, inhibiting AKT activation, reducing autophagy, and impairing cytoskeletal integrity─synergistically sensitizing tumors to radiation. This strategy combined with 6 Gy radiation achieved 82.5% tumor suppression in conventional U251 models and 60.4% in radioresistant U87 models, significantly outperforming the clinical radiosensitizer sodium glycididazole. This strategy provides a paradigm for overcoming GBM radioresistance by leveraging bioresponsive nanoscale transformations and lysosomal targeting.
No takes yet. Share an insight, caveat, or question.
Che et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: