4.4 Review

Combating Hepatitis C Virus by Targeting MicroRNA-122 Using Locked Nucleic Acids

期刊

CURRENT GENE THERAPY
卷 12, 期 4, 页码 301-306

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/156652312802083558

关键词

Clinical trials; gene targeting; hepatitis C virus; locked nucleic acids; microRNA-mRNA interactions; viral gene expression

资金

  1. NIH [AI069000, AI47365, 5T32 AI007328]
  2. American Liver Foundation (ALF)
  3. National CIHR Research Training Program in Hepatitis C (NCRTP-HepC)

向作者/读者索取更多资源

MicroRNAs have been predicted to regulate the stability and translation of many target mRNAs that are involved in modulating disease outcome. Thus, valuable strategies to enhance or to diminish the function of microRNAs are needed to manipulate microRNA-mediated target gene expression. Recently, it has become apparent that one class of antisense oligonucleotides, locked nucleic acids, can be used to sequester microRNAs in the liver of a variety of animals including humans, opening the possibility of applying locked nucleic acid-mediated gene therapy. This review summarizes the success of sequestration of liver-specific microRNA miR-122 by antisense locked nucleic acids and their use in combating hepatitis C virus in clinical trials.

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