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DOI: 10.1055/s-2008-1081296
Phytochemicals as Protectors Against Ultraviolet Radiation: Versatility of Effects and Mechanisms
Publication History
Received: March 26, 2008
Revised: May 16, 2008
Accepted: May 22, 2008
Publication Date:
11 August 2008 (online)
Abstract
Ultraviolet (UV) radiation is one of the most abundant carcinogens in our environment, and the development of non-melanoma skin cancers, the most common type of human malignancy worldwide, represents one of the major consequences of excessive exposure. Because of growing concerns that the level of UV radiation is increasing as a result of depletion of the stratospheric ozone and climate change, the development of strategies for protection of the skin is an urgent need. Many phytochemicals that belong to various families of secondary metabolites, such as alkaloids (caffeine, sanguinarine), flavonoids [(−)-epigallocatechin 3-gallate, genistein, silibinin], carotenoids (β-carotene, lycopene), and isothiocyanates (sulforaphane), offer exciting platforms for the development of such protective strategies. These phytochemicals have been consumed by humans for many centuries as part of plant-rich diets and are presumed to be of low toxicity, an essential requirement for a chemoprotective agent. Mechanistically, they affect multiple signalling pathways and protect against UV radiation-inflicted damage by their ability to act as direct and indirect antioxidants, as well as anti-inflammatory and immunomodulatory agents. Such ”pluripotent character” is a critical prerequisite for an agent that is designed to counteract the multiple damaging effects of UV radiation. Especially attractive are inducers of the Keap1/Nrf2/ARE pathway, which controls the gene expression of proteins whose activation leads to enhanced protection against oxidants and electrophiles. Such protection is comprehensive, long-lasting, and unlikely to cause pro-oxidant effects or interfere with the synthesis of vitamin D.
Abbreviations
AP-1:activator protein 1
ARE:antioxidant response element
COX-2:cyclooxygenase 2
EGG:epigallocatechin 3-gallate
EGF:epidermal growth factor
GSH:glutathione
iNOS:inducible nitric oxide synthase
Keap1:Kelch-like ECH-associated protein 1
IL:inerleukin
MAPK:mitogen-activated protein kinase
MMP:matrix metalloprotease
NF-κB:nuclear factor-κB
NQO1:NAD(P)H:quinone oxidoreductase 1
Nrf2:nuclear factor-erythroid 2-related factor 2
ODC:ornithine decarobxylase
PCNA:proliferating cell nuclear antigen
ROS:reactive oxygen species
TPA:12-O-tetradecanoylphorbol 13-acetate
UV:ultraviolet
Key words
caffeine - epigallocatechin 3-gallate - lycopene - silibinin - skin cancer - sulforaphane
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Albena T. Dinkova-Kostova
University of Dundee
Biomedical Research Centre
Ninewells Hospital and Medical School, Level 5
Dundee DD1 9SY
Scotland
United Kingdom
Phone: +44-1382-740-045
Fax: +44-1382-669-993
Email: a.dinkovakostova@dundee.ac.uk