Source:http://linkedlifedata.com/resource/pubmed/id/20138242
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-8-6
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pubmed:abstractText |
Hepatoma (hepatocellular carcinoma) is the most common type of malignant tumor originating in the liver and has a relatively low 5-year survival rate. The development of hepatoma-targeted therapy is needed to increase treatment efficiency and to reduce the incidence of undesirable side effects. In this study we developed a novel hepatoma-targeted gene delivery system. The gene delivery system was prepared by combining a human liver cell-specific bionanocapsule (BNC) and a tumor cell-specific gene regulation polymer, which responds to hyperactivated protein kinase C alpha in hepatoma cells. The complex of the polymer-DNA with BNCs was delivered into cells and tissues. The developed system showed increased transfection efficiency and resulted in cell-specific gene expression in hepatoma cells and tissues (HuH-7), but no gene expression in normal human hepatocytes or human epidermoid tumor cells (A431). The combination of a tumor cell-specific gene regulation system responding to protein kinase C alpha and BNCs showed excellent potential for the selective treatment of hepatomas. The system could be a useful method with applications in hepatoma-specific gene therapy and molecular imaging. From the clinical editor: Hepatocellular carcinoma is the most common type of malignant tumor in the liver with a low 5-year survival rate. In this study, a novel hepatoma-targeted gene delivery system was prepared by combining a human liver cell-specific bionanocapsule and a tumor cell-specific gene regulation polymer, which responds to hyperactivated protein kinase C (PKC)a in hepatoma cells. The system could be a useful in hepatoma-specific gene therapy and molecular imaging.
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pubmed:commentsCorrections | |
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 |
Aug
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pubmed:issn |
1549-9642
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pubmed:author |
pubmed-author:AsaiDaisukeD,
pubmed-author:IjuinMoekoM,
pubmed-author:JunByungdugB,
pubmed-author:KangJeong-HunJH,
pubmed-author:KatayamaYoshikiY,
pubmed-author:KimJong-HwanJH,
pubmed-author:KurodaShun'ichiS,
pubmed-author:MoriTakeshiT,
pubmed-author:NiidomeTakuroT,
pubmed-author:OishiJunJ,
pubmed-author:TanizawaKatsuyukiK,
pubmed-author:ToitaRikiR
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pubmed:copyrightInfo |
2010 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
583-9
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pubmed:dateRevised |
2011-9-14
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pubmed:meshHeading |
pubmed-meshheading:20138242-Animals,
pubmed-meshheading:20138242-Carcinoma, Hepatocellular,
pubmed-meshheading:20138242-Gene Expression Regulation,
pubmed-meshheading:20138242-Gene Therapy,
pubmed-meshheading:20138242-Gene Transfer Techniques,
pubmed-meshheading:20138242-Hepatocytes,
pubmed-meshheading:20138242-Humans,
pubmed-meshheading:20138242-Liver,
pubmed-meshheading:20138242-Liver Neoplasms,
pubmed-meshheading:20138242-Male,
pubmed-meshheading:20138242-Mice,
pubmed-meshheading:20138242-Nanocapsules,
pubmed-meshheading:20138242-Oligopeptides,
pubmed-meshheading:20138242-Tumor Cells, Cultured
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pubmed:year |
2010
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pubmed:articleTitle |
Hepatoma-targeted gene delivery using a tumor cell-specific gene regulation system combined with a human liver cell-specific bionanocapsule.
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pubmed:affiliation |
Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Fukuoka, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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