Peptide-Functionalized and Drug-Loaded Tomato Bushy Stunt Virus Nanoparticles Counteract Tumor Growth in a Mouse Model of Shh-Dependent Medulloblastoma.
Luca MarchettiFlavia NovelliBarbara TannoSimona LeonardiVeronica Mohamed HizamCaterina ArcangeliLuca SantiSelene BaschieriChiara LicoMariateresa MancusoPublished in: International journal of molecular sciences (2023)
Sonic hedgehog medulloblastoma (SHH-MB) accounts for 25-30% of all MBs, and conventional therapy results in severe long-term side effects. New targeted therapeutic approaches are urgently needed, drawing also on the fields of nanoparticles (NPs). Among these, plant viruses are very promising, and we previously demonstrated that tomato bushy stunt virus (TBSV), functionalized on the surface with CooP peptide, specifically targets MB cells. Here, we tested the hypothesis that TBSV-CooP can specifically deliver a conventional chemotherapeutic drug (i.e., doxorubicin, DOX) to MB in vivo. To this aim, a preclinical study was designed to verify, by histological and molecular methods, if multiple doses of DOX-TBSV-CooP were able to inhibit tumor progression of MB pre-neoplastic lesions, and if a single dose was able to modulate pro-apoptotic/anti-proliferative molecular signaling in full-blown MBs. Our results demonstrate that when DOX is encapsulated in TBSV-CooP, its effects on cell proliferation and cell death are similar to those obtained with a five-fold higher dose of non-encapsulated DOX, both in early and late MB stages. In conclusion, these results confirm that CooP-functionalized TBSV NPs are efficient carriers for the targeted delivery of therapeutics to brain tumors.
Keyphrases
- cell death
- cell proliferation
- cell cycle arrest
- mouse model
- quantum dots
- cancer therapy
- drug delivery
- induced apoptosis
- molecularly imprinted
- small molecule
- emergency department
- anti inflammatory
- cell cycle
- early onset
- poor prognosis
- stem cells
- adverse drug
- high resolution
- single molecule
- endoplasmic reticulum stress
- cell therapy
- oxidative stress
- long non coding rna
- simultaneous determination
- pi k akt
- replacement therapy
- oxide nanoparticles
- chemotherapy induced
- disease virus