Photochemoprevention of ultraviolet B signaling and photocarcinogenesis

被引:236
作者
Afaq, F [1 ]
Adhami, VM [1 ]
Mukhtar, H [1 ]
机构
[1] Univ Wisconsin, Dept Dermatol, Med Sci Ctr, Madison, WI 53706 USA
关键词
photochemoprevention; ultraviolet radiation; signal transduction; p53; PI3K/AKT; NF-kappa B; AP1; MAPK; COX-2; ODC;
D O I
10.1016/j.mrfmmm.2004.07.019
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Exposure to solar radiation, particularly its ultraviolet (UV) B component, has a variety of harmful effects on human health, Some of these effects include sunburn cell formation, basal and squamous cell cancers, melanoma, cataracts, photoaging of the skin, and immune suppression. Amongst these various adverse effects of UV radiation, skin cancer is of the greatest concern. Over the years, changes in lifestyle has led to a significant increase in the amount of UV radiation that people receive, and this consequently has led to a surge in the incidence of skin cancer. The development of skin cancer is a complex multistage phenomenon involving three distinct stages exemplified by initiation, promotion and progression stages. Each of these stages is mediated via alterations in various cellular, biochemical, and molecular changes. Initiation, the first step in the carcinogenesis process is essentially an irreversible step in which genetic alterations occur in genes that ultimately leads to DNA modification and fixation of mutation. Tumor promotion is the essential process in cancer development involving clonal expansion of initiated cells giving rise to pre-malignant and then to malignant lesions, essentially by alterations in signal transduction pathways. Tumor progression involves the conversion of pre-malignant and malignant lesions into an invasive and potentially metastatic malignant tumor. All these processes for skin cancer development involve stimulation of DNA synthesis, DNA damage and proliferation, inflammation, immunosuppression, epidermal hyperplasia, cell cycle dysregulation, depletion of antioxidant defenses, impairment of signal transduction pathways, induction of cyclooxygenase, increase in prostaglandin synthesis, and induction of ornithine decarboxylase. Photocheinoprevention has been appreciated as a viable approach to reduce the occurrence of skin cancer and in recent years, the use of agents, especially botanical antioxidants, present in the common diet and beverages consumed by human population have gained considerable attention as photochemopreventive agents for human use. Many such agents have also found a place in skin care products. Although this is more common in oriental countries, its popularity is significantly growing in western countries. In this article, we have summarized the available information of laboratory studies on UVB-mediated signaling that can be exploited as targets for photochemoprevention. We suggest that the use of skin care products supplemented with proven chemopreventive agents in conjunction with the use of sunscreens along with educational efforts may be an effective strategy for reducing UV-induced photodamage and skin cancer in humans. The mechanistic basis for the use of such products is discussed. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:153 / 173
页数:21
相关论文
共 188 条
[1]   A role for NF-κB-dependent gene transactivation in sunburn [J].
Abeyama, K ;
Eng, W ;
Jester, JV ;
Vink, AA ;
Edelbaum, D ;
Cockerell, CJ ;
Bergstresser, PR ;
Takashima, A .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (12) :1751-1759
[2]   Suppression of ultraviolet B exposure-mediated activation of NF-κB in normal human keratinocytes by resveratrol [J].
Adhami, VM ;
Afaq, F ;
Ahmad, N .
NEOPLASIA, 2003, 5 (01) :74-82
[3]   Suppression of UVB-induced phosphorylation of mitogen-activated protein kinases and nuclear factor kappa B by green tea polyphenol in SKH-1 hairless mice [J].
Afaq, F ;
Ahmad, N ;
Mukhtar, H .
ONCOGENE, 2003, 22 (58) :9254-9264
[4]   Inhibition of ultraviolet B-mediated activation of nuclear factor κB in normal human epidermal keratinocytes by green tea Constituent (-)-epigallocatechin-3-gallate [J].
Afaq, F ;
Adhami, VM ;
Ahmad, N ;
Mukhtar, H .
ONCOGENE, 2003, 22 (07) :1035-1044
[5]   Prevention of short-term ultraviolet B radiation-mediated damages by resveratrol in SKH-1 hairless mice [J].
Afaq, F ;
Adhami, VM ;
Ahmad, N .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 186 (01) :28-37
[6]   Botanical antioxidants for chemoprevention of photocarcinogenesis [J].
Afaq, F ;
Adhami, VM ;
Ahmad, N ;
Mukhtar, H .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2002, 7 :D784-D792
[7]   Effects of solar radiation on cutaneous detoxification pathways [J].
Afaq, F ;
Mukhtar, H .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2001, 63 (1-3) :61-69
[8]   PROTECTION AGAINST ULTRAVIOLET-B RADIATION-INDUCED EFFECTS IN THE SKIN OF SKH-1 HAIRLESS MICE BY A POLYPHENOLIC FRACTION ISOLATED FROM GREEN TEA [J].
AGARWAL, R ;
KATIYAR, SK ;
KHAN, SG ;
MUKHTAR, H .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1993, 58 (05) :695-700
[9]   Green tea polyphenol epigallocatechin-3-gallate differentially modulates nuclear factor κB in cancer cells versus normal cells [J].
Ahmad, N ;
Gupta, S ;
Mukhtar, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 376 (02) :338-346
[10]   A definitive role of ornithine decarboxylase in photocarcinogenesis [J].
Ahmad, N ;
Gilliam, AC ;
Katiyar, SK ;
O'Brien, TG ;
Mukhtar, H .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (03) :885-892