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In vivo Reversal of P‐Glycoprotein‐Mediated Multidrug Resistance by Efficient Delivery of Stealth TM RNAi
Author(s) -
Xiao Hong,
Wu Zhuo,
Shen Hong,
Luo AiLan,
Yang YuFei,
Li XiaoBo,
Zhu DongYa
Publication year - 2008
Publication title -
basic and clinical pharmacology and toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.805
H-Index - 90
eISSN - 1742-7843
pISSN - 1742-7835
DOI - 10.1111/j.1742-7843.2008.00296.x
Subject(s) - rna interference , p glycoprotein , gene silencing , multiple drug resistance , transfection , gene expression , biology , electroporation , microbiology and biotechnology , gene , messenger rna , transcription (linguistics) , in vivo , cancer research , genetic enhancement , drug resistance , rna , genetics , linguistics , philosophy
P‐Glycoprotein‐mediated multidrug resistance (MDR) is a major hurdle in cancer therapy. P‐Glycoprotein is a 170 KD protein encoded by the MDR1 gene. Over‐expression of P‐glycoprotein is considered one of the characteristics of the MDR phenotype, thus down‐regulation of the MDR1 gene expression will circumvent MDR partly. RNA interference (RNAi) is a process that can result in sequence‐specific gene silencing by cleavage target mRNA. Electroporation has been demonstrated to be a promising and efficient method for gene delivery and has been successfully applied in gene therapy. In our study, by using electric pulse to delivery Stealth TM RNAi into nude mice NCI‐H460 tumour xenografts, we successfully inhibited MDR1 both at the mRNA level as determined by reverse transcription–polymerase chain reaction and at the protein level as determined by immunohistochemistry. Furthermore, by administration of navelbine after transfection with Stealth TM RNAi targeted on the MDR1 gene, its depression to tumour xenografts dramatically improved by nine times. These studies demonstrate that through electrotransfection of Stealth TM RNAi, P‐glycoprotein‐mediated MDR can be reversed.