Source:http://linkedlifedata.com/resource/pubmed/id/17804728
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2007-9-6
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pubmed:abstractText |
Magnetic nanoparticles (MNP) with a diameter of 8 nm were modified with different generations of polyamidoamine (PAMAM) dendrimers and mixed with antisense survivin oligodeoxynucleotide (asODN). The MNP then formed asODN-dendrimer-MNP composites, which we incubated with human tumor cell lines such as human breast cancer MCF-7, MDA-MB-435, and liver cancer HepG2 and then analyzed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, quantitative reverse transcription-PCR, Western blotting, laser confocal microscopy, and high-resolution transmission electron microscopy. Results showed that the asODN-dendrimer-MNP composites were successfully synthesized, can enter into tumor cells within 15 min, caused marked down-regulation of the survivin gene and protein, and inhibited cell growth in dose- and time-dependent means. No.5 generation of asODN-dendrimer-MNP composites exhibits the highest efficiency for cellular transfection and inhibition. These results show that PAMAM dendrimer-modified MNPs may be a good gene delivery system and have potential applications in cancer therapy and molecular imaging diagnosis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/BIRC5 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Dendrimers,
http://linkedlifedata.com/resource/pubmed/chemical/Inhibitor of Apoptosis Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Microtubule-Associated Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Oligodeoxyribonucleotides, Antisense
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0008-5472
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
67
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
8156-63
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:17804728-Cell Proliferation,
pubmed-meshheading:17804728-Cell Survival,
pubmed-meshheading:17804728-Dendrimers,
pubmed-meshheading:17804728-Gene Therapy,
pubmed-meshheading:17804728-Gene Transfer Techniques,
pubmed-meshheading:17804728-HL-60 Cells,
pubmed-meshheading:17804728-Humans,
pubmed-meshheading:17804728-Inhibitor of Apoptosis Proteins,
pubmed-meshheading:17804728-Magnetics,
pubmed-meshheading:17804728-Metal Nanoparticles,
pubmed-meshheading:17804728-Microtubule-Associated Proteins,
pubmed-meshheading:17804728-Models, Biological,
pubmed-meshheading:17804728-Neoplasm Proteins,
pubmed-meshheading:17804728-Neoplasms,
pubmed-meshheading:17804728-Oligodeoxyribonucleotides, Antisense,
pubmed-meshheading:17804728-Treatment Outcome,
pubmed-meshheading:17804728-Tumor Cells, Cultured
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pubmed:year |
2007
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pubmed:articleTitle |
Dendrimer-modified magnetic nanoparticles enhance efficiency of gene delivery system.
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pubmed:affiliation |
Department of Bio-Nano-Science and Engineering, National Key Laboratory of Nano/Micro Fabrication Technology, Shanghai Jiao Tong University, Shanghai, PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Evaluation Studies
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