Related Experiment Video
Updated: Apr 16, 2026

A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
[Molecular alterations in melanoma and targeted therapies]
1AP-HP, Hôpital Saint-Louis, Laboratoire de pharmacologie-génétique, 1, avenue Claude-Vellefaux, 75010 Paris, France; Inserm, U976, 1, avenue Claude-Vellefaux, 75010 Paris, France; Université Paris Diderot, Sorbonne Paris Cité, UMR-S-976, 1, avenue Claude-Vellefaux, 75010 Paris, France.
Abstract:
Melanoma is a skin cancer whose incidence is increasing steadily. The recent discovery of frequent and recurrent genetic alterations in cutaneous melanoma allowed a molecular classification of tumors into distinct subgroups, and paved the way for targeted therapy. Several signaling pathways are involved in the progression of this disease with oncogenic mutations affecting signaling pathways: MAPK, PI3K, cAMP and cyclin D1/CDK4. In each of these pathways, several potential therapeutic targets have been identified and specific inhibitors have already been developed and have shown clinical efficacy. The use of these inhibitors is often conditioned by tumors genotyping. In France, melanomas genotyping is supported by the platforms of the National Cancer Institute (INCA), which implemented a national program ensuring access to innovation for personalized medicine. The identification of new targets in melanoma supplies a very active dynamic development of innovative molecules contributing to changing the therapeutic landscape of this pathology.
Insights
Melanoma, a growing skin cancer, is now molecularly classified, enabling targeted therapies. Tumor genotyping, supported by national programs, guides treatment with effective inhibitors for specific molecular subgroups.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Context:
- Melanoma incidence is rising globally.
- Genetic alterations drive melanoma progression.
- Targeted therapies offer new treatment avenues.
Purpose:
- To review the molecular landscape of melanoma.
- To highlight key signaling pathways implicated in melanoma.
- To discuss the role of targeted therapies and genotyping.
Summary:
- Recurrent genetic alterations in cutaneous melanoma enable molecular classification into distinct subgroups.
- Key signaling pathways (MAPK, PI3K, cAMP, cyclin D1/CDK4) harbor oncogenic mutations.
- Therapeutic targets and specific inhibitors have been developed, with efficacy often dependent on tumor genotyping.
- National programs, like INCA in France, facilitate access to genotyping for personalized medicine.
Impact:
- Advances in melanoma treatment through personalized medicine.
- Development of innovative molecules targeting specific melanoma pathways.
- Changing therapeutic landscape for melanoma patients.
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