CTX-CNF1 Recombinant Protein Selectively Targets Glioma Cells In Vivo.


Journal

Toxins
ISSN: 2072-6651
Titre abrégé: Toxins (Basel)
Pays: Switzerland
ID NLM: 101530765

Informations de publication

Date de publication:
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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Auteurs

Eleonora Vannini (E)

Neuroscience Institute, National Research Council (CNR), via G. Moruzzi 1, 56124 Pisa, Italy.
Fondazione Umberto Veronesi, 20122 Milan, Italy.

Elisabetta Mori (E)

Scuola Normale Superiore, 56126 Pisa, Italy.

Elena Tantillo (E)

Neuroscience Institute, National Research Council (CNR), via G. Moruzzi 1, 56124 Pisa, Italy.

Gudula Schmidt (G)

Medizinische Fakultät, Institut für Experimentelle und Klinische Pharmakologie und Toxikologie, University of Freiburg, 79085 Freiburg, Germany.

Matteo Caleo (M)

Neuroscience Institute, National Research Council (CNR), via G. Moruzzi 1, 56124 Pisa, Italy.
Department of Biomedical Sciences, University of Padua, 35122 Padua, Italy.

Mario Costa (M)

Neuroscience Institute, National Research Council (CNR), via G. Moruzzi 1, 56124 Pisa, Italy.

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Classifications MeSH