Progress in antisense technology

被引:361
作者
Crooke, ST [1 ]
机构
[1] ISIS Pharmaceut, Carlsbad, CA 92008 USA
来源
ANNUAL REVIEW OF MEDICINE | 2004年 / 55卷
关键词
RNA; therapeutics; RNase H; RNAi; double-strand RNase;
D O I
10.1146/annurev.med.55.091902.104408
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Antisense technology exploits oligonucleotide analogs to bind to target RNAs via Watson-Crick hybridization. Once bound, the antisense agent either disables or induces the degradation of the target RNA. Antisense agents can also alter splicing. During the past decade, much has been learned about the basic mechanisms of antisense, the medicinal chemistry, and the pharmacologic, pharmacokinetic, and toxicologic properties of antisense molecules. Antisense technology has proven valuable in gene functionalization and target validation. With one drug marketed, Vitravene((R)), and approximately 20 antisense drugs in clinical development, it appears that antisense drugs may prove important in the treatment of a wide range of diseases.
引用
收藏
页码:61 / 95
页数:35
相关论文
共 176 条
[1]   SUPPRESSION OF NEOINTIMAL SMOOTH-MUSCLE CELL ACCUMULATION IN-VIVO BY ANTISENSE CDC2 AND CDK2 OLIGONUCLEOTIDES IN RAT CAROTID-ARTERY [J].
ABE, J ;
ZHOU, W ;
TAGUCHI, J ;
TAKUWA, N ;
MIKI, K ;
OKAZAKI, H ;
KUROKAWA, K ;
KUMADA, M ;
TAKUWA, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 198 (01) :16-24
[2]   PHARMACOKINETICS, BIODISTRIBUTION, AND STABILITY OF OLIGODEOXYNUCLEOTIDE PHOSPHOROTHIOATES IN MICE [J].
AGRAWAL, S ;
TEMSAMANI, J ;
TANG, JY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) :7595-7599
[3]   OLIGODEOXYNUCLEOSIDE PHOSPHORAMIDATES AND PHOSPHOROTHIOATES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS [J].
AGRAWAL, S ;
GOODCHILD, J ;
CIVEIRA, MP ;
THORNTON, AH ;
SARIN, PS ;
ZAMECNIK, PC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7079-7083
[4]  
[Anonymous], RIBONUCLEASES STRUCT
[5]   ANTIVIRAL ACTIVITY OF A PHOSPHOROTHIOATE OLIGONUCLEOTIDE COMPLEMENTARY TO RNA OF THE HUMAN CYTOMEGALOVIRUS MAJOR IMMEDIATE-EARLY REGION [J].
AZAD, RF ;
DRIVER, VB ;
TANAKA, K ;
CROOKE, RM ;
ANDERSON, KP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (09) :1945-1954
[6]   ANTISENSE OLIGONUCLEOTIDES DIRECTED AGAINST P53 HAVE ANTIPROLIFERATIVE EFFECTS UNRELATED TO EFFECTS ON P53 EXPRESSION [J].
BARTON, CM ;
LEMOINE, NR .
BRITISH JOURNAL OF CANCER, 1995, 71 (03) :429-437
[7]  
Bennett CF, 2001, ANTISENSE DRUG TECHNOLOGY: PRINCIPLES, STRATEGIES, AND APPLICATIONS, P291
[8]  
BENNETT CF, 1992, MOL PHARMACOL, V41, P1023
[9]  
Bennett CF, 1993, J LIPOSOME RES, V3, P85
[10]  
BENNETT CF, 1996, THERAPEUTIC MODULATI, P171