Literature DB >> 11948195

Evaluating the specificity of antisense oligonucleotide conjugates. A DNA array analysis.

Anna Astriab Fisher1, Dongjiu Ye, Dimitri S Sergueev, Michael H Fisher, Barbara Ramsay Shaw, Rudolph L Juliano.   

Abstract

Antisense oligonucleotides are potentially powerful tools for selective control of cellular and viral gene expression. Crucial to successful application of this approach is the specificity of the oligonucleotide for the chosen RNA target. Here we apply DNA array technology to examine the specificity of antisense oligonucleotide treatments. The molecules used in these studies consisted of phosphorothioate oligomers linked to the Antennapedia (Ant) delivery peptide. The antisense oligonucleotide component was complementary to a site flanking the AUG of the MDR1 message, which codes for P-glycoprotein, a membrane ATPase associated with multidrug resistance in tumor cells. Using a DNA array of 2059 genes, we analyzed cellular responses to molecules comprised of Ant peptide-oligonucleotide conjugates, as well as to the Ant peptide alone. Besides the expected reduction in MDR1 message level, 37 other genes (approximately 2% of those tested) showed changes of comparable magnitude. The validity of the array results was confirmed for selected genes using Northern blots to assess messenger RNA levels. These results suggest that studies using antisense oligonucleotide technology to modulate gene expression need to be interpreted with caution.

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Year:  2002        PMID: 11948195     DOI: 10.1074/jbc.M203347200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  13 in total

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5.  Direct comparison of the specificity of gene silencing using antisense oligonucleotides and RNAi.

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6.  Inhibition of MDR1 gene expression by chimeric HNA antisense oligonucleotides.

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Journal:  Nucleic Acids Res       Date:  2004-08-17       Impact factor: 16.971

7.  The transcription factor CREB has no non-redundant functions in hepatic glucose metabolism in mice.

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8.  Mammalian cell penetration, siRNA transfection, and DNA transfection by supercharged proteins.

Authors:  Brian R McNaughton; James J Cronican; David B Thompson; David R Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-23       Impact factor: 11.205

9.  A status report on RNAi therapeutics.

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Review 10.  Epigenetic manipulation of gene expression: a toolkit for cell biologists.

Authors:  Rudy L Juliano; Vidula R Dixit; Hyunmin Kang; Tai Young Kim; Yuko Miyamoto; Dong Xu
Journal:  J Cell Biol       Date:  2005-06-20       Impact factor: 10.539

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