CRE-decoy oligonucleotide-inhibition of gene expression and tumor growth

被引:32
作者
Cho-Chung, YS [1 ]
Park, YG [1 ]
Nesterova, M [1 ]
Lee, YN [1 ]
Cho, YS [1 ]
机构
[1] NCI, Cellular Biochem Sect, Tumor Immunol & Biol Lab, NIH, Bethesda, MD 20892 USA
关键词
cAMP; transcription factor-decoy oligonucleotides; CRE; Ap-1; p53; tumor growth; gene expression;
D O I
10.1023/A:1007144618589
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nucleic acid molecules with high affinities for a target transcription factor can be introduced into cells as decoy cis-elements to bind these factors and alter gene expression. This review discusses a synthetic single-stranded palindromic oligonucleotide, which self-hybridizes to form a duplex/hairpin and competes with cAMP response element (CRE) enhancers for binding transcription factors. This oligonucleotide inhibits CRE- and Ap-1-directed gene transcription and promotes growth inhibition in vitro and in vivo in a broad spectrum of cancer cells, without adversely affecting normal cell growth. Evidence presented here suggests that the CRE-decoy oligonucleotide can provide a powerful new means of combating cancers, viral diseases, and other pathological conditions by regulating the expression of cAMP-responsive genes.
引用
收藏
页码:29 / 34
页数:6
相关论文
共 54 条
  • [1] Agadir A, 1997, CANCER RES, V57, P3444
  • [2] Mixed-backbone oligonucleotides as second generation antisense oligonucleotides: In vitro and in vivo studies
    Agrawal, S
    Jiang, ZW
    Zhao, QY
    Shaw, D
    Cai, QY
    Roskey, A
    Channavajjala, L
    Saxinger, C
    Zhang, RW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) : 2620 - 2625
  • [3] Antisense therapeutics
    Agrawal, S
    Zhao, QY
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1998, 2 (04) : 519 - 528
  • [4] Cross-talk between cAMP and p53-generated signals in induction of differentiation and apoptosis in steroidogenic granulosa cells
    Amsterdam, A
    KerenTal, I
    Aharoni, D
    [J]. STEROIDS, 1996, 61 (04) : 252 - 256
  • [5] ACTIVATION OF CAMP AND MITOGEN RESPONSIVE GENES RELIES ON A COMMON NUCLEAR FACTOR
    ARIAS, J
    ALBERTS, AS
    BRINDLE, P
    CLARET, FX
    SMEAL, T
    KARIN, M
    FERAMISCO, J
    MONTMINY, M
    [J]. NATURE, 1994, 370 (6486) : 226 - 229
  • [6] ELECTRON-MICROSCOPY REVEALS THAT TRANSCRIPTION FACTOR-TFIIIA BENDS 5S-DNA
    BAZETTJONES, DP
    BROWN, ML
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (01) : 336 - 341
  • [7] SPECIFIC RECOGNITION OF CRUCIFORM DNA BY NUCLEAR-PROTEIN HMG1
    BIANCHI, ME
    BELTRAME, M
    PAONESSA, G
    [J]. SCIENCE, 1989, 243 (4894) : 1056 - 1059
  • [8] REGULATION OF GENE-EXPRESSION WITH DOUBLE-STRANDED PHOSPHOROTHIOATE OLIGONUCLEOTIDES
    BIELINSKA, A
    SHIVDASANI, RA
    ZHANG, LQ
    NABEL, GJ
    [J]. SCIENCE, 1990, 250 (4983) : 997 - 1000
  • [9] Modulation of tax and PKA-mediated expression of HTLV-I promoter via cAMP response element binding and modulator proteins CREB and CREM
    Bodor, J
    Walker, W
    Flemington, E
    Spetz, AL
    Habener, JF
    [J]. FEBS LETTERS, 1995, 377 (03) : 413 - 418
  • [10] IAC REPRESSOR CAN REGULATE EXPRESSION FROM A HYBRID-SV40 EARLY PROMOTER CONTAINING A LAC OPERATOR IN ANIMAL-CELLS
    BROWN, M
    FIGGE, J
    HANSEN, U
    WRIGHT, C
    JEANG, KT
    KHOURY, G
    LIVINGSTON, DM
    ROBERTS, TM
    [J]. CELL, 1987, 49 (05) : 603 - 612