Literature DB >> 15104896

Use of antisense oligonucleotides in functional genomics and target validation.

Lingamanaidu V Ravichandran1, Nicholas M Dean, Eric G Marcusson.   

Abstract

With the completion of sequencing of the human genome, a great deal of interest has been shifted toward functional genomics-based research for identification of novel drug targets for treatment of various diseases. The major challenge facing the pharmaceutical industry is to identify disease-causing genes and elucidate additional roles for genes of known functions. Gene functionalization and target validation are probably the most important steps involved in identifying novel potential drug targets. This review focuses on recent advances in antisense technology and its use for rapid identification and validation of new drug targets. The significance and applicability of this technology as a beginning of the drug discovery process are underscored by relevant cell culture-based assays and positive correlation in specific animal disease models. Some of the antisense inhibitors used to validate gene targets are themselves being developed as drugs. The current clinical trials based on such leads that were identified in a very short time further substantiate the importance of antisense technology-based functional genomics as an integral part of target validation and drug target identification.

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Year:  2004        PMID: 15104896     DOI: 10.1089/154545704322988058

Source DB:  PubMed          Journal:  Oligonucleotides        ISSN: 1545-4576


  4 in total

1.  Small interfering RNAs containing full 2'-O-methylribonucleotide-modified sense strands display Argonaute2/eIF2C2-dependent activity.

Authors:  Bryan A Kraynack; Brenda F Baker
Journal:  RNA       Date:  2005-11-21       Impact factor: 4.942

2.  Synthetic antisense oligodeoxynucleotides to transiently suppress different nucleus- and chloroplast-encoded proteins of higher plant chloroplasts.

Authors:  Emine Dinç; Szilvia Z Tóth; Gert Schansker; Ferhan Ayaydin; László Kovács; Dénes Dudits; Gyozo Garab; Sándor Bottka
Journal:  Plant Physiol       Date:  2011-10-06       Impact factor: 8.340

3.  Formulation of polylactide-co-glycolic acid nanospheres for encapsulation and sustained release of poly(ethylene imine)-poly(ethylene glycol) copolymers complexed to oligonucleotides.

Authors:  Shashank R Sirsi; Rebecca C Schray; Margaret A Wheatley; Gordon J Lutz
Journal:  J Nanobiotechnology       Date:  2009-04-07       Impact factor: 10.435

4.  Modulation of p53 expression using antisense oligonucleotides complementary to the 5'-terminal region of p53 mRNA in vitro and in the living cells.

Authors:  Agnieszka Gorska; Agata Swiatkowska; Mariola Dutkiewicz; Jerzy Ciesiolka
Journal:  PLoS One       Date:  2013-11-11       Impact factor: 3.240

  4 in total

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