Intraventricular SHH inhibition proves efficient in SHH medulloblastoma mouse model and prevents systemic side effects.
Catena KresbachLea HolstMelanie SchoofTara LevenCarolin GöbelSina NeyaziJacqueline TischendorfCarolin LooseAntonina WrzeszczTimur YorganStefan RutkowskiUlrich SchüllerPublished in: Neuro-oncology (2023)
We conclude that intraventricular application of a SHH pathway inhibitor combines the advantages of a specific treatment agent with precise drug delivery and might evolve as a promising new way of targeted treatment for SHH MB patients.