Importance of the form of topical vitamin E for prevention of photocarcinogenesis
Abstract
With increasing solar ultraviolet (UV)-B radiation reaching the Earth's surface and the incidence of skin cancer rising steadily, there is an ever-increasing need to determine agents that modulate photocarcinogenesis and to understand the mechanisms underlying this modulation. Our laboratory has demonstrated that topical application of the dl-alpha-tocopherol form of vitamin E to mice prevents skin cancer and the immunosuppression induced by UVB irradiation. However, dl-alpha-tocopherol has limited stability at room temperature. The current study was designed to ask whether the thermostable esters of vitamin E, alpha-tocopheryl acetate, or alpha-tocopheryl succinate prevent skin cancer and immunosuppression induced in mice by UV radiation. In the alpha-tocopheryl acetate study, skin cancers developed in 70% of UVB-irradiated control mice and in 90%, 73%, and 90% of mice receiving topical applications of 12.5, 25, and 50 mg of dl-alpha-tocopheryl acetate, respectively. In the alpha-tocopheryl succinate study, skin cancer developed in 59.3% of control UVB-irradiated mice and in 82%, 100%, and 81.5% of mice treated with 2.5, 12.5, and 25 mg d-alpha-tocopheryl succinate, respectively. Thus neither alpha-tocopheryl acetate nor alpha-tocopheryl succinate prevented photocarcinogenesis. At 12.5 and 25 mg/treatment, alpha-tocopheryl acetate and alpha-tocopheryl succinate, respectively, enhanced photocarcinogenesis (p = 0.0114 and 0.0262, respectively, log rank test). On the basis of h…
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a-Tocopheryl acetate and a-tocopheryl succinate are less effective than a-tocopherol in protecting the skin against UV-induced erythema, photoaging, immunosuppression, and carcinogenesis.
“However, both substitutes are less effective than a-tocopherol in protecting the skin against UV-induced erythema, photoaging, immunosuppression, and carcinogenesis (124,125,127).”
From Photoprotection: a Review of the Current and Future Technologies (2010) · cites this paper as [127]
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Self-citation
- Authors
- Gensler, H. L., Aickin, M., Peng, Y., & Xu, M.
- Affiliations
- University of Arizona (US)
- University of Arizona Cancer Center (US)
- Arizona Cancer Center
- Venue
- Nutrition and Cancer
- Publisher
- Informa UK Limited
- Published
- 1996-01
- Volume
- 26
- Issue
- 2
- Pages
- 183-191
- ISSN
- 0163-5581 (ISSN-L)
- 1532-7914
- OpenAlex
- W2047729113
- Cited by
- 78
- References
- 0
- Citations by year
- 2025: 1 · 2024: 2 · 2021: 2 · 2020: 1 · 2017: 2 · 2016: 3 · 2015: 3 · 2014: 1 · 2013: 2 · 2012: 2
- FWCI
- 5.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nutrition and Cancer (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (CA 27502, CA-44504, P01CA027502)
- Topics
- Health Sciences › Medicine › Dermatology › Skin Protection and Aging
- Health Sciences › Medicine › Epidemiology › Nonmelanoma Skin Cancer Studies
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Keywords
- vitamin E, alpha-tocopherol acetate, alpha-tocopheryl succinate, DL-alpha-tocopherol, photocarcinogenesis, UVB-induced skin cancer, topical vitamin E, vitamin E esters, immunosuppression, skin cancer prevention, vitamin E stability
- MeSH terms
- Administration, Topical, Animals, Esterification, Female, Immunity, Mice, Inbred BALB C, Radiation-Protective Agents, Skin, Skin Neoplasms, Specific Pathogen-Free Organisms, Ultraviolet Rays, Vitamin E, alpha-Tocopherol, Tocopherols, Mice
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