Topical applications of caffeine or (-)-epigallocatechin gallate (EGCG) inhibit carcinogenesis and selectively increase apoptosis in UVB-induced skin tumors in mice
Open accessAbstract
SKH-1 hairless mice were irradiated with ultraviolet B (UVB) twice weekly for 20 weeks. These tumor-free mice, which had a high risk of developing skin tumors during the next several months, were then treated topically with caffeine (6.2 μmol) or (−)-epigallocatechin gallate (EGCG; 6.5 μmol) once a day 5 days a week for 18 weeks in the absence of further treatment with UVB. Topical applications of caffeine to these mice decreased the number of nonmalignant and malignant skin tumors per mouse by 44% and 72%, respectively. Topical applications of EGCG decreased the number of nonmalignant and malignant tumors per mouse by 55% and 66%, respectively. Immunohistochemical analysis showed that topical applications of caffeine or EGCG increased apoptosis as measured by the number of caspase 3-positive cells in nonmalignant skin tumors by 87% or 72%, respectively, and in squamous cell carcinomas by 92% or 56%, respectively, but there was no effect on apoptosis in nontumor areas of the epidermis. Topical applications of caffeine or EGCG had a small inhibitory effect on proliferation in nonmalignant tumors as measured by BrdUrd labeling (16–22%), and there was also a similar, but nonsignificant, inhibitory effect on proliferation in malignant tumors. The results suggest a need for further studies to determine whether topical applications of caffeine or EGCG can inhibit sunlight-induced skin cancer in humans.
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Green tea polyphenols protect against photocarcinogenesis.
“| (epicatechin-3-gallate), | from tea | Photocarcinogenesis | | + | (117-119) |”
From Photoprotection: a Review of the Current and Future Technologies (2010) · cites this paper as [119]
The Abstract reports that topical EGCG, a tea constituent, reduced skin tumors in UVB-pretreated mice, and the Discussion describes inhibition of UVB-induced carcinogenesis. This supports the claim for EGCG in mice, but the study does not establish protection by green tea polyphenols as a class or in humans. (LLM, conf=0.82)
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Self-citation
- Authors
- Lu, Y.-P., Lou, Y.-R., Xie, J.-G., Peng, Q.-Y., Liao, J., Yang, C. S., Huang, M.-T., & Conney, A. H.
- Affiliations
- Rutgers, The State University of New Jersey (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2002-08-30
- Volume
- 99
- Issue
- 19
- Pages
- 12455-12460
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC129466
- OpenAlex
- W2066022538
- Cited by
- 316
- References
- 1
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 4 · 2023: 7 · 2022: 11 · 2021: 6 · 2020: 16 · 2019: 9 · 2018: 5 · 2017: 8 · 2016: 17 · 2015: 7 · 2014: 11 · 2013: 21 · 2012: 26
- FWCI
- 22.06
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (CA88961)
- National Cancer Institute (P01CA088961, CA 88961)
- Topics
- Health Sciences › Medicine › Dermatology › Skin Protection and Aging
- Health Sciences › Medicine › Epidemiology › Nonmelanoma Skin Cancer Studies
- Health Sciences › Medicine › Pathology and Forensic Medicine › Tea Polyphenols and Effects
- Keywords
- caffeine, epigallocatechin gallate, topical application, skin carcinogenesis, apoptosis, caspase-3, squamous cell carcinoma, cell proliferation, SKH-1 mice, photoprotection
- MeSH terms
- Administration, Topical, Animals, Bromodeoxyuridine, Caffeine, Catechin, Female, Mice, Hairless, Neoplasms, Radiation-Induced, Skin Neoplasms, Tea, Ultraviolet Rays, Apoptosis, Caspases, Mice, Caspase 3
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