Antisense therapeutics in chronic myeloid leukaemia: the promise, the progress and the problems

被引:30
作者
Clark, RE [1 ]
机构
[1] Royal Liverpool Univ Hosp, Univ Dept Haematol, Liverpool L7 8XP, Merseyside, England
关键词
chronic myeloid leukaemia; antisense oligodeoxyribonucleotides;
D O I
10.1038/sj.leu.2401677
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA sequences which are complementary or 'antisense' to a target mRNA can inhibit expression of that mRNA's protein product. Antisense therapeutics has therefore received attention for inhibiting oncogenes in haematological malignancy, in particular in chronic myeloid leukaemia. However, it is now becoming clear that antisense therapeutics is considerably more problematic than was naively initially assumed. In this article, some of these difficulties are discussed, together with the achievements in CML so far. Considerable further research is required in order to define an optimal antisense therapeutics strategy for clinical use.
引用
收藏
页码:347 / 355
页数:9
相关论文
共 133 条
  • [1] DIFFERENTIAL COMPLEMENTATION OF BCR-ABL POINT MUTANTS WITH C-MYC
    AFAR, DEH
    GOGA, A
    MCLAUGHLIN, J
    WITTE, ON
    SAWYERS, CL
    [J]. SCIENCE, 1994, 264 (5157) : 424 - 426
  • [2] PHARMACOKINETICS, BIODISTRIBUTION, AND STABILITY OF OLIGODEOXYNUCLEOTIDE PHOSPHOROTHIOATES IN MICE
    AGRAWAL, S
    TEMSAMANI, J
    TANG, JY
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) : 7595 - 7599
  • [3] Antisense oligonucleotides: Towards clinical trials
    Agrawal, S
    [J]. TRENDS IN BIOTECHNOLOGY, 1996, 14 (10) : 376 - 387
  • [4] Second-generation antisense oligonucleotides: Structure-activity relationships and the design of improved signal-transduction inhibitors
    Altmann, KH
    Fabbro, D
    Dean, NM
    Geiger, T
    Monia, BP
    Muller, M
    Nicklin, P
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 1996, 24 (03) : 630 - 637
  • [5] Anderson WF, 1998, NATURE, V392, P25
  • [6] *ANT RES DEV 3, 1993, 2 ANT RES DEV 3, P153
  • [7] Barton C, 1997, J CLIN ONCOL, V15, P408
  • [8] BEDI A, 1994, BLOOD, V83, P2038
  • [9] BEDI A, 1993, BLOOD, V81, P2898
  • [10] ISOLATION AND CHARACTERIZATION OF THE HUMAN CELLULAR MYC GENE-PRODUCT
    BEIMLING, P
    BENTER, T
    SANDER, T
    MOELLING, K
    [J]. BIOCHEMISTRY, 1985, 24 (23) : 6349 - 6355