Radiation-Triggered Selenium-Engineered Mesoporous Silica Nanocapsules for RNAi Therapy in Radiotherapy-Resistant Glioblastoma.
Xiang-Long TangZhen WangYandong XieYuyang LiuKun YangTaiping LiHong ShenMengjie ZhaoJuan JinHong XiaoHongyi LiuNing GuPublished in: ACS nano (2023)
Radiotherapy-resistant glioblastoma (rrGBM) remains a significant clinical challenge because of high infiltrative growth characterized by activation of antiapoptotic signal transduction. Herein, we describe an efficiently biodegradable selenium-engineered mesoporous silica nanocapsule, initiated by high-energy X-ray irradiation and employed for at-site RNA interference (RNAi) to inhibit rrGBM invasion and achieve maximum therapeutic benefit. Our radiation-triggered RNAi nanocapsule showed high physiological stability, good blood-brain barrier transcytosis, and potent rrGBM accumulation. An intratumoral RNAi nanocapsule permitted low-dose X-ray radiation-triggered dissociation for cofilin-1 knockdown, inhibiting rrGBM infiltration. More importantly, tumor suppression was further amplified by electron-affinity aminoimidazole products converted from metronidazole polymers under X-ray radiation-exacerbated hypoxia, which sensitized cell apoptosis to ionizing radiation by fixing reactive oxygen species-induced DNA lesions. In vivo experiments confirmed that our RNAi nanocapsule reduced tumor growth and invasion, prolonging survival in an orthotopic rrGBM model. Generally, we present a promising radiosensitizer that would effectively improve rrGBM-patient outcomes with low-dose X-ray irradiation.
Keyphrases
- blood brain barrier
- low dose
- radiation induced
- high resolution
- dual energy
- electron microscopy
- reactive oxygen species
- early stage
- high dose
- radiation therapy
- cell migration
- cerebral ischemia
- computed tomography
- drug delivery
- locally advanced
- signaling pathway
- squamous cell carcinoma
- magnetic resonance imaging
- mesenchymal stem cells
- mass spectrometry
- stem cells
- magnetic resonance
- circulating tumor
- brain injury
- nucleic acid
- cell free
- drug induced
- oxidative stress
- free survival