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Updated: Apr 30, 2026

Assessment of Oxidative Damage in the Primary Mouse Ocular Surface Cells/Stem Cells in Response to Ultraviolet-C UV-C Damage
Published on: February 15, 2020
Cyclooxygenases: mediators of UV-induced skin cancer and potential targets for prevention
Craig A Elmets1, Johnathan J Ledet2, Mohammad Athar3
1Department of Dermatology, University of Alabama at Birmingham, Birmingham, Alabama, USA; UAB Skin Diseases Research Center, University of Alabama at Birmingham, Birmingham, Alabama, USA; UAB Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama, USA; Birmingham Veterans Administration Medical Center, Birmingham, Alabama, USA.
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.
Insights
Non-melanoma skin cancers are common, and current prevention methods are insufficient. Blocking the cyclooxygenase-2 (COX-2) enzyme shows promise for preventing these UV-induced skin cancers.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Non-melanoma skin cancers (NMSCs) are highly prevalent malignancies.
- Current UV radiation avoidance and protection methods have not curbed rising incidence rates.
- Cyclooxygenase-2 (COX-2), an enzyme in prostaglandin synthesis, is implicated in NMSC development.
Purpose of the Study:
- To investigate the role of COX-2 in the pathogenesis of NMSC.
- To evaluate the potential of COX-2 inhibitors as chemopreventive agents against NMSC.
Main Methods:
- Preclinical studies using genetically modified animals lacking COX-2.
- Studies involving pharmacological COX-2 inhibitors in UV-induced skin carcinogenesis models.
- Epidemiological studies examining human populations and UV radiation exposure.
Main Results:
- Animals deficient in COX-2 or treated with COX-2 inhibitors developed fewer UV-induced skin tumors.
- UV radiation exposure increases COX-2 expression in human skin.
- Evidence suggests a significant role for COX-2 in UV-induced skin cancer.
Conclusions:
- Pharmacological agents that inhibit COX-2 may serve as effective chemopreventive agents for NMSC.
- Targeting COX-2 represents a potential strategy to prevent UV-induced skin cancers.
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