Abstract |
The phototoxicity of ketoprofen (KP), a non-steroidal anti-inflammatory drug, has recently attracted considerable attention, because it is photolabile and undergoes degradation when irradiated by sunlight to induce various skin diseases. The present study shows that combination of UVB irradiation with KP induced the cytotoxicity and suppressed DNA synthesis in HaCaT cells in a concentration-dependent manner. UVB-irradiated KP inhibited the cell growth and induced G2/M cell cycle arrest by modulating the levels of cdc2, cyclin B1, Chk1, Tyr15-phosphorylated cdc2 and p21. It also provoked a striking accumulation of cyclin B1-cdc2-p21 complexes, concomitantly with an increase in the levels of Tyr15-phosphorylated cdc2 and p21 protein. The presence of KP accentuated the apoptotic response to UVB radiation in HaCaT cells as evidenced by DAPI staining. The apoptotic process was associated with activation of caspase-9, caspase-3 and cleavage of PARP, and this activation could be prevented by a specific caspase-3 inhibitor. Taken together, our results suggest that KP-photoinduced apoptosis may be a useful approach to reduce or prevent skin carcinogenesis.
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Authors | Shicheng Liu, Hideo Mizu, Hitoshi Yamauchi |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 364
Issue 3
Pg. 650-5
(Dec 21 2007)
ISSN: 1090-2104 [Electronic] United States |
PMID | 17964538
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Apoptosis
(drug effects, radiation effects)
- Cell Division
(drug effects, radiation effects)
- Cell Proliferation
- Dose-Response Relationship, Drug
- Dose-Response Relationship, Radiation
- G2 Phase
(drug effects, radiation effects)
- Keratinocytes
(cytology, drug effects, radiation effects)
- Ketoprofen
(administration & dosage)
- Oxidative Stress
(drug effects, physiology, radiation effects)
- Radiation Dosage
- Radiation Tolerance
(drug effects)
- Ultraviolet Rays
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