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.

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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