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Updated: May 22, 2026

Pharmacologic Induction of Epidermal Melanin and Protection Against Sunburn in a Humanized Mouse Model
Published on: September 7, 2013
Non-steroidal anti-inflammatory drugs and melanoma
Virginia Sanz-Motilva1, Antonio Martorell-Calatayud, Eduardo Nagore
1Dermatology Department, Hospital Universitario 12 de Octubre, Avenida de Córdoba s/n. 28026, Madrid, Spain. vsanzmotilva@hotmail.com
Abstract:
Inflammation is an important contributor to the development and progression of all human cancers. Inflammatory lipid metabolites, prostaglandins, formed from arachidonic acid by prostaglandin H synthases commonly called cyclooxygenases (COXs), bind to specific receptors that activate signaling pathways driving to the development and progression of tumors. Inhibitors of prostaglandin formation, COX inhibitors, including non-steroidal anti-inflammatory drugs (NSAIDs), are well documented agents that inhibit tumor growth and prevent tumor development specially due to long-term use. NSAIDs also alter gene expression independently of COX inhibition which also appear to contribute to the anti-tumorigenic activity of these drugs. In a dermatologic point of view, most investigations are oriented to improve the current knowledge related to the pathogenesis of malignant melanoma, a prevalent skin cancer characterized by a rapid progression with frequent metastases and a poor response to the different available treatments. In the present issue we review the role of inflammation in cutaneous malignant melanoma and its impact on cancer pathogenesis. This topic represents an exciting new area of research, and could potentially result in new targets for melanoma therapy in the future.
Insights
Inflammation fuels cancer growth, particularly in skin cancer like melanoma. COX inhibitors, such as NSAIDs, show anti-tumor effects by blocking inflammatory prostaglandins and altering gene expression.
Area of Science:
- Oncology
- Dermatology
- Inflammation Research
Background:
- Inflammation is a key factor in the development and progression of human cancers.
- Prostaglandins, formed by cyclooxygenases (COXs), are inflammatory lipid metabolites that promote tumor growth.
- Non-steroidal anti-inflammatory drugs (NSAIDs) are known to inhibit tumor growth and development.
Purpose of the Study:
- To review the role of inflammation in cutaneous malignant melanoma pathogenesis.
- To explore the impact of inflammation on melanoma progression.
- To identify potential new therapeutic targets for melanoma.
Main Methods:
- Literature review on inflammation in cancer.
- Focus on prostaglandin synthesis and cyclooxygenase (COX) inhibition.
- Examination of NSAID mechanisms beyond COX inhibition.
Main Results:
- Inflammatory lipid metabolites (prostaglandins) activate signaling pathways driving tumor progression.
- NSAIDs inhibit tumor growth and development, partly through COX inhibition.
- NSAIDs also exhibit anti-tumorigenic activity via COX-independent gene expression alterations.
Conclusions:
- Inflammation plays a significant role in the pathogenesis of cutaneous malignant melanoma.
- Understanding inflammation's impact may lead to novel therapeutic strategies for melanoma.
- Further research into inflammation and melanoma could yield new treatment targets.
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