CHAPTER 60 – Antisense therapy

作者: S CROOKE

DOI: 10.1016/B978-012689663-3/50064-8

关键词: BioinformaticsGeneFunction (biology)Antisense therapyOligonucleotideRNABiologyAntisense TechnologyFirst generation

摘要: This chapter provides an overview of antisense technology, which exploits oligonucleotide analogs (typically 15–20 nucleotides) to bind cognate RNA sequences through Watson–Crick hybridization resulting in the destruction or disablement target RNA. Thus, technology represents a “new pharmacology” that continues advance. Clinical experience with first generation drugs now exceeds several thousand patients, and number studies suggest therapeutic activity. Second dramatically improved properties are available for clinical trials. Antisense has also been automated such it is useful as tool determine gene function, being used biological roles various cytokine related genes. Further, inhibitors cytokines genes progressing evaluations potential.

参考文章(161)
Kazuyoshi Saito, Yvette van Kooyk, Sumiya Eto, Yoshiya Tanaka, Shinichiro Mine, Carl G. Figdor, Atsushi Wake, Hideyasu Hirano, Junichi Tsukada, Megumi Aso, Koichi Fujii, Constitutive chemokine production results in activation of leukocyte function-associated antigen-1 on adult T-Cell leukemia cells Blood. ,vol. 91, pp. 3909- 3919 ,(1998) , 10.1182/BLOOD.V91.10.3909
John P. Sheehan, Hao-Chang Lan, Phosphorothioate Oligonucleotides Inhibit the Intrinsic Tenase Complex Blood. ,vol. 92, pp. 1617- 1625 ,(1998) , 10.1182/BLOOD.V92.5.1617
Gunther Hartmann, Anne Krug, Kerstin Waller-Fontaine, Stefan Endres, Oligodeoxynucleotides Enhance Lipopolysaccharide-Stimulated Synthesis of Tumor Necrosis Factor: Dependence on Phosphorothioate Modification and Reversal by Heparin Molecular Medicine. ,vol. 2, pp. 429- 438 ,(1996) , 10.1007/BF03401902
Paul S. Miller, Non-ionic Antisense Oligonucleotides ChemInform. ,vol. 23, pp. 79- 95 ,(1989) , 10.1007/978-1-349-10869-5_5
Butler M, Bennett Cf, Stecker K, Cellular distribution of phosphorothioate oligodeoxynucleotides in normal rodent tissues. Laboratory Investigation. ,vol. 77, pp. 379- 388 ,(1997)
Hidetoshi Arima, Mamiko Takahashi, Yukihiko Aramaki, Takatoshi Sakamoto, Kazuhiro Yuda, Katsuhiko Akiyama, Takeshi Goto, Seishi Tsuchiya, Design of potent phosphorothioate antisense oligonucleotides directed to human interleukin 10 gene product and their evaluation of antisense activity in U937 cells. Pharmaceutical Research. ,vol. 16, pp. 1163- 1171 ,(1999) , 10.1023/A:1018964625977
P. L. Nicklin, S. J. Craig, J. A. Phillips, Pharmacokinetic Properties of Phosphorothioates in Animals — Absorption, Distribution, Metabolism and Elimination Handbook of experimental pharmacology. ,vol. 131, pp. 141- 168 ,(1998) , 10.1007/978-3-642-58785-6_4
WAYNE M. GALBRAITH, WILLIAM C. HOBSON, PATRICIA C. GICLAS, PAUL J. SCHECHTER, SUDHIR AGRAWAL, Complement activation and hemodynamic changes following intravenous administration of phosphorothioate oligonucleotides in the monkey. Antisense research and development. ,vol. 4, pp. 201- 206 ,(1994) , 10.1089/ARD.1994.4.201
JOHN M. DAGLE, DANIEL L. WEEKS, JOSEPH A. WALDER, Pathways of degradation and mechanism of action of antisense oligonucleotides in Xenopus laevis embryos. Antisense research and development. ,vol. 1, pp. 11- 20 ,(1991) , 10.1089/ARD.1991.1.11