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Updated: May 31, 2026
![Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate (DMBA-TPA)](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60445.jpg&w=3840&q=50)
Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate (DMBA-TPA)
Published on: December 19, 2019
Focus on skin cancer association and progression under TNF antagonist therapy
Claudine Piérard-Franchimont1, Gérald E Piérard, Pascale Quatresooz
1University Hospital Sart Tilman, Department of Dermatopathology, CHU Sart Tilman, B-4000 Liège, Belgium. gerald.pierard@ulg.ac.be
Introduction:
Basal and squamous cell carcinomas are the most common non-melanoma skin cancers (NMSC) in humans. Their prevalence is higher in immunocompromized patients. Results of some animal experiments have indicated that TNF acts both as a tumour promotor and an inductor of apoptosis.
Areas Covered:
Peer-reviewed articles about human skin cancers possibly related to TNF antagonists. The occurrence and growth kinetics of NMSC are possibly increased in some patients under TNF antagonist therapy. Other issues of such biological treatment suggested include the activation of other distinct skin malignancies, including malignant melanoma. Benign melanocytic tumours appear to be boosted as well. At present, most of the reported findings only represent anecdotal case reports. The influence of cumulative co-factors must not be neglected, particularly the effect of other therapies administered to the patients. The occurrence of antibodies to some TNF antagonists may decrease both the treatment efficacy and the risk of skin cancer progression.
Expert Opinion:
More research needs to be performed in order to firmly establish and understand the risk of anti-TNF biologicals in the area of human skin cancers. At present, NMSC progression appears to be boosted on areas of skin field cancerization. Benign melanocytic naevi may develop as well.
Insights
Tumor necrosis factor (TNF) antagonists may increase the risk of non-melanoma skin cancers (NMSC) and benign melanocytic tumors. Further research is needed to confirm these findings in human skin cancer patients.
Area of Science:
- Dermatology
- Oncology
- Immunology
Background:
- Basal cell carcinoma and squamous cell carcinoma are the most common human non-melanoma skin cancers (NMSC).
- NMSC prevalence is higher in immunocompromised individuals.
- Tumor necrosis factor (TNF) has demonstrated roles in both tumor promotion and apoptosis induction in animal models.
Purpose of the Study:
- To investigate the potential association between TNF antagonist therapy and the development or progression of human skin cancers.
- To review existing literature on the effects of TNF antagonists on non-melanoma skin cancers, melanoma, and benign melanocytic tumors.
Main Methods:
- A review of peer-reviewed articles concerning human skin cancers potentially linked to TNF antagonists.
- Analysis of reported cases of NMSC and other skin malignancies in patients undergoing TNF antagonist therapy.
- Consideration of confounding factors such as cumulative co-exposures and other patient therapies.
Main Results:
- Some patient reports suggest an increased occurrence and altered growth kinetics of NMSC in individuals treated with TNF antagonists.
- There are suggestions of increased risk for other skin malignancies, including malignant melanoma, and benign melanocytic tumors.
- Most current evidence consists of anecdotal case reports, necessitating cautious interpretation.
Conclusions:
- Further research is essential to definitively establish and comprehend the risks associated with anti-TNF biologicals concerning human skin cancers.
- Current observations suggest that NMSC progression may be enhanced in areas of skin field cancerization.
- The development of benign melanocytic nevi is also a potential outcome observed during anti-TNF therapy.
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11:02The Three-Dimensional Human Skin Reconstruct Model: a Tool to Study Normal Skin and Melanoma Progression
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16:07Determination of the Relative Potency of an Anti-TNF Monoclonal Antibody (mAb) by Neutralizing TNF Using an In Vitro Bioanalytical Method
Published on: September 16, 2017
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