Source:http://linkedlifedata.com/resource/pubmed/id/17007568
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006142,
umls-concept:C0011209,
umls-concept:C0026809,
umls-concept:C0036043,
umls-concept:C0162969,
umls-concept:C0348016,
umls-concept:C0522537,
umls-concept:C0580822,
umls-concept:C1099354,
umls-concept:C1450054,
umls-concept:C1547300,
umls-concept:C1548760,
umls-concept:C1550594,
umls-concept:C2346689
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pubmed:issue |
10
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pubmed:dateCreated |
2006-10-24
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pubmed:abstractText |
Overexpression of RhoA in cancer indicates a poor prognosis, because of increased tumor cell proliferation and invasion and tumor angiogenesis. We showed previously that anti-RhoA small interfering RNA (siRNA) inhibited aggressive breast cancer more effectively than conventional blockers of Rho-mediated signaling pathways. This study reports the efficacy and lack of toxicity of intravenously administered encapsulated anti-RhoA siRNA in chitosan-coated polyisohexylcyanoacrylate (PIHCA) nanoparticles in xenografted aggressive breast cancers (MDA-MB-231). The siRNA was administered every 3 days at a dose of 150 or 1500 microg/kg body weight in nude mice. This treatment inhibited the growth of tumors by 90% in the 150-microg group and by even more in the 1500-microg group. Necrotic areas were observed in tumors from animals treated with anti-RhoA siRNA at 1500 microg/kg, resulting from angiogenesis inhibition. In addition, this therapy was found to be devoid of toxic effects, as evidenced by similarities between control and treated animals for the following parameters: body weight gain; biochemical markers of hepatic, renal, and pancreatic function; and macroscopic appearance of organs after 30 days of treatment. Because of its efficacy and the absence of toxicity, it is suggested that this strategy of anti-RhoA siRNA holds significant promise for the treatment of aggressive cancers.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1043-0342
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1019-26
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pubmed:meshHeading |
pubmed-meshheading:17007568-Animals,
pubmed-meshheading:17007568-Breast Neoplasms,
pubmed-meshheading:17007568-Cell Line, Tumor,
pubmed-meshheading:17007568-Chitosan,
pubmed-meshheading:17007568-Humans,
pubmed-meshheading:17007568-Infusion Pumps,
pubmed-meshheading:17007568-Mice,
pubmed-meshheading:17007568-Nanoparticles,
pubmed-meshheading:17007568-Neoplasm Transplantation,
pubmed-meshheading:17007568-Neoplasms,
pubmed-meshheading:17007568-Neovascularization, Pathologic,
pubmed-meshheading:17007568-RNA, Small Interfering,
pubmed-meshheading:17007568-rhoA GTP-Binding Protein
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pubmed:year |
2006
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pubmed:articleTitle |
Intravenous delivery of anti-RhoA small interfering RNA loaded in nanoparticles of chitosan in mice: safety and efficacy in xenografted aggressive breast cancer.
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pubmed:affiliation |
Laboratoire de Recherche MERCI (Micro-Environnement et Régulation Cellulaire Intégrée), Faculté de Médecine et Pharmacie, Rouen, France. pillejea@etu.univ-rouen.fr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Evaluation Studies
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