Abstract |
Pretreatment of SKH-1 mice with p.o.-administered 0.6% green tea (6 mg of lyophilized tea solids/ml) or 0.044% caffeine (0.44 mg/ml; concentration present in 0.6% green tea) for 2 weeks enhanced UV-induced increases in the number of p53-positive cells, p21(WAF1/CIP1)-positive cells, and apoptotic sunburn cells in the epidermis. These effects of p.o.-administered green tea or caffeine on early adaptive responses to UV provide the first demonstration of in vivo up-regulation of a tumor suppressor gene by a chemopreventive agent. The stimulatory effect of green tea and caffeine on UV-induced increases in the number of p53-positive cells, p21(WAF1/CIP1)-positive cells, and apoptotic sunburn cells may play a role in the inhibitory effects of tea and caffeine on UV-induced carcinogenesis.
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Authors | Y P Lu, Y R Lou, X H Li, J G Xie, D Brash, M T Huang, A H Conney |
Journal | Cancer research
(Cancer Res)
Vol. 60
Issue 17
Pg. 4785-91
(Sep 01 2000)
ISSN: 0008-5472 [Print] United States |
PMID | 10987287
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Anticarcinogenic Agents
- Cdkn1a protein, mouse
- Cyclin-Dependent Kinase Inhibitor p21
- Cyclins
- Tea
- Tumor Suppressor Protein p53
- Caffeine
- DNA
- Bromodeoxyuridine
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Topics |
- Adaptation, Biological
(drug effects, radiation effects)
- Administration, Oral
- Animals
- Anticarcinogenic Agents
(pharmacology)
- Apoptosis
(drug effects, radiation effects)
- Bromodeoxyuridine
(metabolism)
- Caffeine
(pharmacology)
- Cell Division
(drug effects, radiation effects)
- Cyclin-Dependent Kinase Inhibitor p21
- Cyclins
(biosynthesis, genetics)
- DNA
(metabolism)
- Epidermis
(drug effects, metabolism, radiation effects)
- Female
- Mice
- Mice, Hairless
- Stimulation, Chemical
- Sunburn
(metabolism, pathology)
- Tea
- Tumor Suppressor Protein p53
(biosynthesis, genetics)
- Ultraviolet Rays
(adverse effects)
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