http://www.cnr.it/ontology/cnr/individuo/prodotto/ID301630
In vivo targeting of cutaneous melanoma using an melanoma stimulating hormone-engineered human protein cage with fluorophore and magnetic resonance imaging tracers (Articolo in rivista)
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- Label
- In vivo targeting of cutaneous melanoma using an melanoma stimulating hormone-engineered human protein cage with fluorophore and magnetic resonance imaging tracers (Articolo in rivista) (literal)
- Anno
- 2015-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1166/jbn.2015.1946 (literal)
- Alternative label
Vannucci, Luca E.; Falvo, Elisabetta; Failla, Cristina Maria; Carbo, Miriam; Fornara, Manuela; Canese, Rossella; Cecchetti, Serena; Rajsiglova, Lenka; Stakheev, Dmitry; K?í?an, Jiri; Boffi, Alberto; Carpinelli, Giulia; Morea, Veronica; Ceci, Pierpaolo (2015)
In vivo targeting of cutaneous melanoma using an melanoma stimulating hormone-engineered human protein cage with fluorophore and magnetic resonance imaging tracers
in Journal of biomedical nanotechnology (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Vannucci, Luca E.; Falvo, Elisabetta; Failla, Cristina Maria; Carbo, Miriam; Fornara, Manuela; Canese, Rossella; Cecchetti, Serena; Rajsiglova, Lenka; Stakheev, Dmitry; K?í?an, Jiri; Boffi, Alberto; Carpinelli, Giulia; Morea, Veronica; Ceci, Pierpaolo (literal)
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- Institute of Microbiology of the Academy of Sciences of the Czech Republic; CNR - National Research Council of Italy, Institute of Molecular Biology and Pathology; IRCCS Istituto Dermopatico dell'Immacolata; Universita degli Studi di Roma La Sapienza; Istituto Superiore Di Sanita, Rome; Istituto Italiano di Tecnologia (literal)
- Titolo
- In vivo targeting of cutaneous melanoma using an melanoma stimulating hormone-engineered human protein cage with fluorophore and magnetic resonance imaging tracers (literal)
- Abstract
- Nanoparticle (NP)-based materials are promising agents for enhancing cancer diagnosis and treatment. Once functionalized for selective targeting of tumor-expressed molecules, they can specifically deliver drugs and diagnostic molecules inside tumor cells. In the present work, we evaluated the in vivo melanoma-targeting ability of a nanovector (HFt-MSHPEG) based on human protein ferritin (HFt), functionalized with both melanoma-targeting melanoma stimulating hormone (?-MSH) and stabilizing poly(ethylene glycol) (PEG) molecules. Independent and complementary techniques, such as whole-specimen confocal microscopy and magnetic resonance imaging, were used to detect in vivo localization of NP constructs with suitable tracers (i.e., fluorophores or magnetic metals). Targeted HFt-MSH-PEG NPs accumulated persistently at the level of primary melanoma and with high selectivity with respect to other organs. Melanoma localization of untargeted HFt-PEG NPs, which lack the ?-MSH moiety, was less pronounced. Furthermore, HFt-MSH-PEG NPs accumulated to a significantly lower extent and with a different distribution in a diverse type of tumor (TS/A adenocarcinoma), which does not express ?-MSH receptors. Finally, in a spontaneous lung metastasis model, HFt-MSH-PEG NPs localized at the metastasis level as well. These results suggest that HFt-MSH-PEG NPs are suitable carriers for selective in vivo delivery of diagnostic or therapeutic agents to cutaneous melanoma. (literal)
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