[Molecular alterations in melanoma and targeted therapies]

Samia Mourah1, Céleste Lebbé2

  • 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.

Bulletin Du Cancer
|March 18, 2015
PubMed

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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