CTX-CNF1 Recombinant Protein Selectively Targets Glioma Cells In Vivo.
Animals
Antineoplastic Agents
/ metabolism
Bacterial Toxins
/ metabolism
Blood-Brain Barrier
/ metabolism
Brain Neoplasms
/ drug therapy
Cell Line, Tumor
Cell Proliferation
/ drug effects
Cellular Senescence
/ drug effects
Escherichia coli Proteins
/ metabolism
Glioma
/ drug therapy
Humans
Injections, Intravenous
Mice, Inbred C57BL
Recombinant Fusion Proteins
/ pharmacology
Scorpion Venoms
/ metabolism
brain tumor
chlorotoxin
cytotoxic necrotizing factor type 1
drug delivery
drug discovery
glioblastoma
glioma
recombinant protein production
Journal
Toxins
ISSN: 2072-6651
Titre abrégé: Toxins (Basel)
Pays: Switzerland
ID NLM: 101530765
Informations de publication
Date de publication:
08 03 2021
08 03 2021
Historique:
received:
14
02
2021
revised:
24
02
2021
accepted:
25
02
2021
entrez:
3
4
2021
pubmed:
4
4
2021
medline:
1
7
2021
Statut:
epublish
Résumé
Current strategies for glioma treatment are only partly effective because of the poor selectivity for tumoral cells. Hence, the necessity to identify novel approaches is urgent. Recent studies highlighted the effectiveness of the bacterial protein cytotoxic necrotizing factor 1 (CNF1) in reducing tumoral mass, increasing survival of glioma-bearing mice and protecting peritumoral neural tissue from dysfunction. However, native CNF1 needs to be delivered into the brain, because of its incapacity to cross the blood-brain barrier (BBB) per se, thus hampering its clinical translation. To allow a non-invasive administration of CNF1, we here developed a chimeric protein (CTX-CNF1) conjugating CNF1 with chlorotoxin (CTX), a peptide already employed in clinics due to its ability of passing the BBB and selectively binding glioma cells. After systemic administration, we found that CTX-CNF1 is able to target glioma cells and significantly prolong survival of glioma-bearing mice. Our data point out the potentiality of CTX-CNF1 as a novel effective tool to treat gliomas.
Identifiants
pubmed: 33800135
pii: toxins13030194
doi: 10.3390/toxins13030194
pmc: PMC7998600
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Bacterial Toxins
0
Escherichia coli Proteins
0
Recombinant Fusion Proteins
0
Scorpion Venoms
0
Chlorotoxin
06UV5RFW57
cytotoxic necrotizing factor type 1
106803-33-2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Fondazione Umberto Veronesi
ID : 2019
Organisme : Associazione Italiana per la Ricerca sul Cancro
ID : IG18925
Organisme : Deutsche Forschungsgemeinschaft
ID : SFB850 project C2
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