Abstract | BACKGROUND: A decoy strategy utilizing oligonucleotides (ODN) containing the specific binding sequence of a certain transcription factor has been developed and is considered to be a potential new class of antigene therapy. However, the application of this new therapeutic modality to skin diseases has not been fully documented. OBJECTIVES: The aim of this work was to examine the effects of the nuclear factor ( NF)-kappaB decoy ODN on UV-elicited skin change. METHODS: Mouse keratinocyte Pam 212 cells were transfected with NF-kappaB decoy ODN to examine the effects of the decoy ODN on ultraviolet (UV) B-induced apoptosis. Tape-stripped rat dorsal skin was treated with an ointment containing NF-kappaB decoy ODN for the examination of the in vivo impact of the decoy ODN on sunburned cell (SBC) formation and UVB erythema. RESULTS: CONCLUSIONS: These data suggest that enhancement of UV-induced apoptosis by NF-kappaB decoy ODN may play a cancer-preventive role by further eliminating photodamaged keratinocytes.
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Authors | S Yokoyama, H Nakano, T Yamazaki, K Tamai, K Hanada, G Takahashi |
Journal | The British journal of dermatology
(Br J Dermatol)
Vol. 153 Suppl 2
Pg. 47-51
(Dec 2005)
ISSN: 0007-0963 [Print] England |
PMID | 16280021
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Hemoglobins
- Melanins
- NF-kappa B
- Oligonucleotides, Antisense
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Topics |
- Administration, Topical
- Animals
- Apoptosis
- Cell Line
- DNA Fragmentation
- Electrophoretic Mobility Shift Assay
- Genetic Therapy
(methods)
- Hemoglobins
(analysis)
- Keratinocytes
(pathology, radiation effects)
- Melanins
(analysis)
- Mice
- NF-kappa B
(genetics, metabolism)
- Oligonucleotides, Antisense
(administration & dosage)
- Rats
- Sunburn
(metabolism, pathology, prevention & control)
- Transfection
(methods)
- Ultraviolet Rays
(adverse effects)
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