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Substituted trans-stilbenes can inhibit or enhance the TPA-induced up-regulation of activator protein-1
- Source :
- BMC Pharmacology
- Publication Year :
- 2008
- Publisher :
- Springer Science and Business Media LLC, 2008.
-
Abstract
- Background The activator protein-1 (AP-1) family of transcription factors contributes to regulation of numerous genes involved in proliferation, apoptosis, and tumorigenesis. A wide array of stimuli can activate AP-1, including pro-inflammatory cytokines, growth factors, tumor promoters and stress. Numerous plant polyphenols have been shown to inhibit the activation of AP-1, which often is ascribed to the anti-oxidant properties of these natural products. Methods In the present study, a library of substituted trans-stilbenes, including polyphenols, was screened for activity against the TPA-induced activation of AP-1 using the Panomics AP-1 Reporter 293 Stable Cell Line, which is designed for screening potential inhibitors or activators. Results Several trans-stilbenes were identified that inhibit TPA-induced activation of AP-1, with IC50 values as low as 0.5 μM. Moreover, some other trans-stilbenes were able to enhance the effects of TPA 2 to 3-fold. Many of the trans-stilbenes identified as inhibitors or enhancers are devoid of anti-oxidant properties. Conclusion The ability of trans-stilbenes to inhibit or enhance the effects of TPA does not depend upon their anti-oxidant properties.
- Subjects :
- Biology
Resveratrol
Antioxidants
Dinoprostone
Cell Line
Mice
chemistry.chemical_compound
Phenols
Downregulation and upregulation
Stilbenes
Animals
Humans
Pharmacology (medical)
Enhancer
Transcription factor
Flavonoids
Pharmacology
Activator (genetics)
Polyphenols
Up-Regulation
Transcription Factor AP-1
Biochemistry
chemistry
Cell culture
Apoptosis
Tetradecanoylphorbol Acetate
Research Article
Transcription Factors
Subjects
Details
- ISSN :
- 14712210
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- BMC Pharmacology
- Accession number :
- edsair.doi.dedup.....9c166d188f977c6474201e635168d505
- Full Text :
- https://doi.org/10.1186/1471-2210-8-19