RETRACTED: Short intefering RNA (siRNA) as a novel therapeutic (Retracted Article)

被引:53
作者
Pushparaj, PN [1 ]
Melendez, AJ [1 ]
机构
[1] Natl Univ Singapore, Dept Physiol, Yong Loo Lin Sch Med, Singapore 117597, Singapore
关键词
cancer; gene knockdown; mammalian cells; neurodegenerative disorders; renal disorders; RNA interference; short interference RNA (siRNA) library; short interference RNA (siRNA) technology; viral infection;
D O I
10.1111/j.1440-1681.2006.04399.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. RNA interference (RNAi) is a robust method of post-transcriptional silencing of genes using double-stranded RNA (dsRNA) with sequence homology driven specificity. The dsRNA can be between 21 and 23 nucleotides long: this is converted to small interfering RNA (siRNA), which then mediates gene silencing by degradation/blocking of translation of the target mRNA. 2. RNA interference provides a simple, fast and cost-effective alternative to existing gene targeting approaches both in vitro and in vivo. The discovery of siRNAs that cause RNAi in mammalian cells opened the door to the therapeutic use of siRNAs. Highly intense research efforts are now aimed at developing siRNAs for therapeutic purposes. 3. Recent advances in the design and delivery of targeting molecules now allow efficient and highly specific gene silencing in mammalian systems. Synthetic siRNA libraries targeting thousands of mammalian genes are publicly available for high-throughput genetic screens for target discovery and validation. Recent studies have demonstrated the clinical potential of aptly designed siRNAs in various types of viral infections, cancer and renal and neurodegenerative disorders. 4. The present review provides insight into the novel therapeutic strategies of siRNA technology, which is the latest development in nucleic acid-based tools for knocking down gene expression, and its potential for silencing genes associated with various human diseases.
引用
收藏
页码:504 / 510
页数:7
相关论文
共 84 条
  • [1] RNA-dependent RNA polymerases, viruses, and RNA silencing
    Ahlquist, P
    [J]. SCIENCE, 2002, 296 (5571) : 1270 - 1273
  • [2] Tolerance for mutations and chemical modifications in a siRNA
    Amarzguioui, M
    Holen, T
    Babaie, E
    Prydz, H
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (02) : 589 - 595
  • [3] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [4] Bernstein E, 2001, RNA, V7, P1509
  • [5] Comparison of antisense oligonucleotides and siRNAs in cell culture and in vivo
    Bertrand, JR
    Pottier, M
    Vekris, A
    Opolon, P
    Maksimenko, A
    Malvy, C
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 296 (04) : 1000 - 1004
  • [6] RNA interference in mammalian cells by chemically-modified RNA
    Braasch, DA
    Jensen, S
    Liu, YH
    Kaur, K
    Arar, K
    White, MA
    Corey, DR
    [J]. BIOCHEMISTRY, 2003, 42 (26) : 7967 - 7975
  • [7] Stable suppression of tumorigenicity by virus-mediated RNA interference
    Brummelkamp, TR
    Bernards, R
    Agami, R
    [J]. CANCER CELL, 2002, 2 (03) : 243 - 247
  • [8] Tissue-specific RNA interference in postimplantation mouse embryos with endoribonuclease-prepared short interfering RNA
    Calegari, F
    Haubensak, W
    Yang, D
    Huttner, WB
    Buchholz, F
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (22) : 14236 - 14240
  • [9] Role of microRNAs in plant and animal development
    Carrington, JC
    Ambros, V
    [J]. SCIENCE, 2003, 301 (5631) : 336 - 338
  • [10] Gene targeting via triple-helix formation
    Casey, BP
    Glazer, PM
    [J]. PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 67, 2001, 67 : 163 - 192