| Literature DB >> 16715379 |
Nedjma Toub1, Jean-Rémi Bertrand, Ali Tamaddon, Hind Elhamess, Hervé Hillaireau, Andrei Maksimenko, Jean Maccario, Claude Malvy, Elias Fattal, Patrick Couvreur.
Abstract
The EWS-Fli1 fusion gene encodes for a chimeric oncogenic transcription factor considered to be the cause of the Ewing sarcoma. The efficiency of small interfering RNAs (siRNAs) targeted toward the EWS-Fli1 transcript (at the junction point type 1) was studied, free or encapsulated into recently developed polyisobutylcyanoacrylate aqueous core nanocapsules. Because this mRNA sequence is only present in cancer cells, it therefore constituted a relevant target. Studies of the intracellular penetration by confocal microscopy in NIH/3T3 EWS-Fli1 cells showed that nanocapsules improved the intracellular penetration of siRNA with mainly a cytoplasmic localization. These biodegradable siRNA-loaded nanocapsules were then tested in vivo on a mice xenografted EWS-Fli1-expressing tumor; they were found to trigger a dose-dependant inhibition of tumor growth after intratumoral injection. A specific inhibition of EWS-Fli1 was observed, too. These findings now open new prospects for the treatment of experimental cancers with junction oncogenes.Entities:
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Year: 2006 PMID: 16715379 DOI: 10.1007/s11095-006-9901-9
Source DB: PubMed Journal: Pharm Res ISSN: 0724-8741 Impact factor: 4.200