中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Downregulation of survivin expression and enhanced chemosensitivity of MCF-7 cells to adriamycin by PDMAE/survivin shRNA complex nanoparticles

文献类型:期刊论文

作者Yang, Yongxin; Gao, Yu; Chen, Lingli; Huang, Yongzhuo; Li, Yaping
刊名INTERNATIONAL JOURNAL OF PHARMACEUTICS
出版日期2011-02-28
卷号405期号:1-2页码:188-195
关键词RNAi shRNA Adriamycin Survivin Poly(2-dimethylaminoethylamine/2-(2-aminoethyoxy)ethoxy)phosphazene (PDMAE)
ISSN号0378-5173
DOI10.1016/j.ijpharm.2010.11.047
文献子类Article
英文摘要Gene silencing mediated by RNA interference (RNAi) presents a promising strategy for gene therapy. The aim of this work is to evaluate a new gene delivery system for downregulation of survivin expression and enhanced chemosensitivity of MCF-7 cells to adriamycin (ADR). A new cationic poly(2-dimethylaminoethylamine/2-(2-aminoethyoxy)ethoxy)phosphazene (PDMAE) with multiple amino groups was synthesized through Michael addition for survivin shRNA (shSur) delivery in MCF-7 cells. PDMAE51/shSur complex nanoparticles with the size of 190 nm and zeta potential of +15 mV achieved maximal suppression of survivin, even superior to PEI25K or poly(2-(2-aminoethyoxy)ethoxy)phosphazene (PAEP) based complex nanoparticles. The significant downregulation of survivin expression was achieved by PDMAE51/shSur nanoparticles. The nuclear localization by confocal laser scanning microscopy (CLSM) and apparent apoptosis peak of cell cycle in MCF-7 cells were observed when transfected by PDMAE51/shSur nanoparticles The combined use of PDMAE51/shSur and ADR enhanced the sensitivity of MCF-7 cells to ADR at a larger extent than that of PEI or PAEP based complex nanoparticles. These results suggested that PDMAE51 could be potential as an efficient and safe gene carrier in RNAi therapeutics and tumor chemotherapy. (C) 2010 Elsevier B.V. All rights reserved.
WOS关键词GENE DELIVERY ; LUNG-CANCER ; TARGETING SURVIVIN ; RNA INTERFERENCE ; IN-VITRO ; SIRNA ; TRANSFECTION ; NUCLEAR ; CARRIER
资助项目National Basic Research Program of China[2010CB934000] ; National Basic Research Program of China[2007CB935800] ; National Natural Science Foundation of China[30925041] ; National Natural Science Foundation of China[30901866] ; National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program"[2009ZX09501-024] ; National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program"[2009ZX09301-001] ; Shanghai Nanomedicine Program[1052nm06300]
WOS研究方向Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000287279400022
出版者ELSEVIER SCIENCE BV
源URL[http://119.78.100.183/handle/2S10ELR8/278597]  
专题药物制剂研究中心
通讯作者Huang, Yongzhuo
作者单位Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Pharmaceut, Shanghai 201203, Peoples R China
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Yang, Yongxin,Gao, Yu,Chen, Lingli,et al. Downregulation of survivin expression and enhanced chemosensitivity of MCF-7 cells to adriamycin by PDMAE/survivin shRNA complex nanoparticles[J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS,2011,405(1-2):188-195.
APA Yang, Yongxin,Gao, Yu,Chen, Lingli,Huang, Yongzhuo,&Li, Yaping.(2011).Downregulation of survivin expression and enhanced chemosensitivity of MCF-7 cells to adriamycin by PDMAE/survivin shRNA complex nanoparticles.INTERNATIONAL JOURNAL OF PHARMACEUTICS,405(1-2),188-195.
MLA Yang, Yongxin,et al."Downregulation of survivin expression and enhanced chemosensitivity of MCF-7 cells to adriamycin by PDMAE/survivin shRNA complex nanoparticles".INTERNATIONAL JOURNAL OF PHARMACEUTICS 405.1-2(2011):188-195.

入库方式: OAI收割

来源:上海药物研究所

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