http://www.cnr.it/ontology/cnr/individuo/prodotto/ID229639
Neuroblastoma tumorigenesis is regulated through the Nm23-H1/h-Prune C-terminal interaction (Articolo in rivista)
- Type
- Label
- Neuroblastoma tumorigenesis is regulated through the Nm23-H1/h-Prune C-terminal interaction (Articolo in rivista) (literal)
- Anno
- 2013-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1038/srep01351 (literal)
- Alternative label
Carotenuto, M ; Pedone, E ; Diana, D ; de Antonellis, P ; Dzeroski, S ; Marino, N ; Navas, L ; Di Dato, V ; Scoppettuolo, MN ; Cimmino, F ; Correale, S ; Pirone, L ; Monti, SM ; Bruder, E ; Zenko, B ; Slavkov, I ; Pastorino, F ; Ponzoni, M ; Schulte, JH ; Schramm, A ; Eggert, A; Westermann, F ; Arrigoni, G ; Accordi, B ; Basso, G ; Saviano, M ; Fattorusso, R ; Zollo, M (2013)
Neuroblastoma tumorigenesis is regulated through the Nm23-H1/h-Prune C-terminal interaction
in Scientific reports (Nature Publishing Group)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Carotenuto, M ; Pedone, E ; Diana, D ; de Antonellis, P ; Dzeroski, S ; Marino, N ; Navas, L ; Di Dato, V ; Scoppettuolo, MN ; Cimmino, F ; Correale, S ; Pirone, L ; Monti, SM ; Bruder, E ; Zenko, B ; Slavkov, I ; Pastorino, F ; Ponzoni, M ; Schulte, JH ; Schramm, A ; Eggert, A; Westermann, F ; Arrigoni, G ; Accordi, B ; Basso, G ; Saviano, M ; Fattorusso, R ; Zollo, M (literal)
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- Ctr Ingn Genet & Biotecnol Avanzate CEINGE, Naples, Italy
Univ Naples Federico II, Dipartimento Med Mol & Biotecnol Med, Naples, Italy
CNR, Ist Biostrutture & Bioimmagini, I-80125 Naples, Italy
Univ Naples 2, Dipartimento Sci Ambientali, Caserta, Italy
Univ Naples Federico II, Sez Clin Chirurg, Dipartimento Sci Clin Vet, Naples, Italy
Univ Basel, Dept Pathol, Basel, Switzerland
Jozef Stefan Inst, Dept Knowledge Technol, Ljubljana 1000, Slovenia
Osped Pediat, Ist Giannina Gaslini, I-16148 Genoa, Italy
Univ Childrens Hosp Essen, Dept Paediat Oncol & Haematol, D-45122 Essen, Germany
German Canc Res Ctr, Dept Tumour Genet, Heidelberg, Germany
Univ Milan, Osped San Raffaele, Dept Pathol, I-20127 Milan, Italy
Univ Padua, Dept Paediat, Haematooncol Lab, Padua, Italy
CNR, Ist Cristallog, I-70126 Bari, Italy
NCI, Womens Canc Sect, Mol Pharmacol Lab, Bethesda, MD 20892 USA (literal)
- Titolo
- Neuroblastoma tumorigenesis is regulated through the Nm23-H1/h-Prune C-terminal interaction (literal)
- Abstract
- Nm23-H1 is one of the most interesting candidate genes for a relevant role in Neuroblastoma pathogenesis. H-Prune is the most characterized Nm23-H1 binding partner, and its overexpression has been shown in different human cancers. Our study focuses on the role of the Nm23-H1/h-Prune protein complex in Neuroblastoma. Using NMR spectroscopy, we performed a conformational analysis of the h-Prune C-terminal to identify the amino acids involved in the interaction with Nm23-H1. We developed a competitive permeable peptide (CPP) to impair the formation of the Nm23-H1/h-Prune complex and demonstrated that CPP causes impairment of cell motility, substantial impairment of tumor growth and metastases formation. Meta-analysis performed on three Neuroblastoma cohorts showed Nm23-H1 as the gene highly associated to Neuroblastoma aggressiveness. We also identified two other proteins (PTPRA and TRIM22) with expression levels significantly affected by CPP. These data suggest a new avenue for potential clinical application of CPP in Neuroblastoma treatment. (literal)
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