Literature DB >> 12084454

Control of alternative splicing by antisense oligonucleotides as a potential chemotherapy: effects on gene expression.

Danielle R Mercatante1, Ryszard Kole.   

Abstract

Expression of alternatively spliced mRNA variants at specific stages of development or in specific cells and tissues contributes to the functional diversity of the human genome. Aberrations in alternative splicing were found as a cause or a contributing factor to the development, progression, or maintenance of various diseases including cancer. The use of antisense oligonucleotides to modify aberrant expression patterns of alternatively spliced mRNAs is a novel means of potentially controlling such diseases. However, to utilize antisense oligonucleotides as molecular chemotherapeutic agents, the global effects of these molecules need to be examined. The advent of gene expression array technology has now made it possible to simultaneously examine changes that occur in the expression levels of several thousand genes in response to antisense treatment. This analysis should help in the development of more specific and efficacious antisense oligonucleotides as molecular therapeutics.

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Year:  2002        PMID: 12084454     DOI: 10.1016/s0925-4439(02)00075-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  12 in total

1.  Modulation of RNA splicing as a potential treatment for cancer.

Authors:  John A Bauman; Ryszard Kole
Journal:  Bioeng Bugs       Date:  2011-05-01

2.  The SR protein SC35 is responsible for aberrant splicing of the E1alpha pyruvate dehydrogenase mRNA in a case of mental retardation with lactic acidosis.

Authors:  Mathieu Gabut; Manuèle Miné; Cécile Marsac; Michèle Brivet; Jamal Tazi; Johann Soret
Journal:  Mol Cell Biol       Date:  2005-04       Impact factor: 4.272

3.  Modulation of mdm2 pre-mRNA splicing by 9-aminoacridine-PNA (peptide nucleic acid) conjugates targeting intron-exon junctions.

Authors:  Takehiko Shiraishi; Jonhard Eysturskarth; Peter E Nielsen
Journal:  BMC Cancer       Date:  2010-06-30       Impact factor: 4.430

4.  Steric inhibition of human immunodeficiency virus type-1 Tat-dependent trans-activation in vitro and in cells by oligonucleotides containing 2'-O-methyl G-clamp ribonucleoside analogues.

Authors:  Stephen C Holmes; Andrey A Arzumanov; Michael J Gait
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

5.  RNA repair restores hemoglobin expression in IVS2-654 thalassemic mice.

Authors:  Saovaros Svasti; Thipparat Suwanmanee; Suthat Fucharoen; Hong M Moulton; Michelle H Nelson; Nobuyo Maeda; Oliver Smithies; Ryszard Kole
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-21       Impact factor: 11.205

6.  Tim50a, a nuclear isoform of the mitochondrial Tim50, interacts with proteins involved in snRNP biogenesis.

Authors:  Hongzhi Xu; Z Brad Somers; Melvin L Robinson; Michael D Hebert
Journal:  BMC Cell Biol       Date:  2005-07-11       Impact factor: 4.241

Review 7.  The future of antisense oligonucleotides in the treatment of respiratory diseases.

Authors:  Marina Ulanova; Alan D Schreiber; A Dean Befus
Journal:  BioDrugs       Date:  2006       Impact factor: 5.807

8.  Efficient Delivery of Antisense Oligonucleotides Using Bioreducible Lipid Nanoparticles In Vitro and In Vivo.

Authors:  Liu Yang; Feihe Ma; Fang Liu; Jinjin Chen; Xuewei Zhao; Qiaobing Xu
Journal:  Mol Ther Nucleic Acids       Date:  2020-01-25       Impact factor: 8.886

9.  Increasing the relative expression of endogenous non-coding Steroid Receptor RNA Activator (SRA) in human breast cancer cells using modified oligonucleotides.

Authors:  Charlton Cooper; Jimin Guo; Yi Yan; Shilpa Chooniedass-Kothari; Florent Hube; Mohammad K Hamedani; Leigh C Murphy; Yvonne Myal; Etienne Leygue
Journal:  Nucleic Acids Res       Date:  2009-05-29       Impact factor: 16.971

10.  Determining the impact of alternative splicing events on transcriptome dynamics.

Authors:  Emmanuelle Wilhelm; François-Xavier Pellay; Arndt Benecke; Brendan Bell
Journal:  BMC Res Notes       Date:  2008-10-24
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