Treatment of actinic keratosis through inhibition of cyclooxygenase-2: Potential mechanism of action of diclofenac sodium 3% in hyaluronic acid 2.5.

Author: CruzSusana Balta, HerranzPedro, ParodiAurora, ThomasGareth J

Paper Details 
Original Abstract of the Article :
Cyclooxygenase-2 (COX-2) and its metabolic product prostaglandin E<sub>2</sub> (PGE<sub>2</sub> ) are induced in response to growth factors, inflammatory cytokines, tumor promoters, activated oncogenes, and, in the skin, ultraviolet (UV) radiation. Accumulating evidence suggests a role for the COX-2...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767532/

データ提供:米国国立医学図書館(NLM)

Diclofenac Sodium: A Promising Treatment for Actinic Keratosis

Actinic keratosis (AK), a precancerous skin condition, is often caused by sun exposure. This article explores the potential of diclofenac sodium 3% in hyaluronic acid 2.5% as a treatment for AK, focusing on its mechanism of action in inhibiting cyclooxygenase-2 (COX-2) and its role in tumorigenesis.

Diclofenac Sodium: Targeting COX-2 for AK Treatment

The article discusses the role of COX-2 and its metabolic product prostaglandin E2 (PGE2) in the development of AK. It explains how diclofenac sodium, a nonsteroidal anti-inflammatory drug (NSAID), inhibits COX-2, potentially leading to the suppression of AK lesions.

Topical Treatments for Skin Cancer Prevention

This article highlights the potential of topical NSAIDs in preventing skin cancer. By understanding the mechanisms of action of these drugs, we can develop more effective and targeted treatments for precancerous skin conditions.

Dr. Camel's Conclusion

The sun's rays, while essential for life, can also be harmful. This research, like a desert traveler seeking shelter from the scorching sun, explores the potential of diclofenac sodium as a shield against the development of AK. By understanding the role of COX-2 in skin cancer, we can develop more effective strategies for preventing and treating this prevalent condition.

Date :
  1. Date Completed 2020-01-14
  2. Date Revised 2021-01-09
Further Info :

Pubmed ID

30523664

DOI: Digital Object Identifier

PMC6767532

SNS
PICO Info
in preparation
Languages

English

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