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Cyclooxygenases: Mediators of UV-induced Skin Cancer and Potential Targets for Prevention

Overview
Publisher Elsevier
Specialty Dermatology
Date 2014 May 9
PMID 24804836
Citations 34
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Abstract

Non-melanoma skin cancers (NMSCs) are among the most common human malignancies. Current methods for their prevention include avoidance of natural and artificial sources of UV radiation and using photoprotective clothing and sunscreens. However, these methods have proven to be inadequate in stemming the rise in skin cancer incidence over the past several years. There is accumulating evidence that cyclooxygenase-2 (COX-2), an enzyme involved in prostaglandin synthesis, may be involved in the pathogenesis of NMSC. In preclinical studies, animals genetically deficient in the COX-2 enzyme or that have been treated with pharmacological inhibitors of COX-2 develop significantly fewer tumors when subjected to a UV-induced skin carcinogenesis protocol compared with control mice. Several epidemiological studies in humans support the concept that this enzyme is intimately involved in UV-induced skin cancer development, and UV radiation is known to augment COX-2 expression in human skin. Recent studies suggest that drugs that block COX-2 expression may prevent the development of NMSCs. Thus, pharmacologic agents that inhibit the enzyme COX-2 may be effective chemopreventive agents for NMSCs.

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References
1.
Brecher A . The role of cyclooxygenase-2 in the pathogenesis of skin cancer. J Drugs Dermatol. 2003; 1(1):44-7. View

2.
Johannesdottir S, Chang E, Mehnert F, Schmidt M, Braae Olesen A, Sorensen H . Nonsteroidal anti-inflammatory drugs and the risk of skin cancer: a population-based case-control study. Cancer. 2012; 118(19):4768-76. DOI: 10.1002/cncr.27406. View

3.
Wilgus T, Koki A, Zweifel B, Kusewitt D, Rubal P, Oberyszyn T . Inhibition of cutaneous ultraviolet light B-mediated inflammation and tumor formation with topical celecoxib treatment. Mol Carcinog. 2003; 38(2):49-58. DOI: 10.1002/mc.10141. View

4.
Rundhaug J, Simper M, Surh I, Fischer S . The role of the EP receptors for prostaglandin E2 in skin and skin cancer. Cancer Metastasis Rev. 2011; 30(3-4):465-80. PMC: 3236828. DOI: 10.1007/s10555-011-9317-9. View

5.
Tober K, Wilgus T, Kusewitt D, Thomas-Ahner J, Maruyama T, Oberyszyn T . Importance of the EP(1) receptor in cutaneous UVB-induced inflammation and tumor development. J Invest Dermatol. 2006; 126(1):205-11. DOI: 10.1038/sj.jid.5700014. View