Abstract
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.
Original language | English |
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Pages (from-to) | 29-34 |
Number of pages | 6 |
Journal | Molecular and Cellular Biochemistry |
Volume | 212 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 2000 |
Externally published | Yes |
Keywords
- Ap-1
- CRE
- Gene expression
- Transcription factor-decoy oligonucleotides
- Tumor growth
- cAMP
- p53
ASJC Scopus subject areas
- Molecular Biology
- Clinical Biochemistry
- Cell Biology