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24, chemin de Borde Rouge –Auzeville – CS52627
31326 Castanet Tolosan CEDEX - France

Dernière mise à jour : Mai 2018

Menu Logo Principal Ministère de l'agriculture et de l'alimentation Ministère de l'enseignement supérieur, de la recherche et de l'innovation Logo_ANR Centre national de la recherche scientifique Fondation pour la recherche sur la biodiversité Laboratoire LABOGENA : analyses génétiques pour les espèces animales Logo_VetAgro Sup ANTAGENE

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New scientific results for targeted therapies for mucosal melanoma

Photo de Vlad Chețan provenant de Pexels
In humans, mucosal melanoma (MM) is a rare and aggressive cancer. The canine model is frequently and spontaneously affected by MM, facilitating sample collection and study of its genetic basis. Through integrative genomic and transcriptomic analysis of 32 canine MM samples, we identified two molecular subgroups of MM with different microenvironment and structural variant (SV) content.

We demonstrated that VS is associated with recurrently amplified regions and identified novel candidate oncogenes (TRPM7, GABPB1 and SPPL2A) for MM. Our results suggest the existence of two molecular subgroups of MM that may benefit from dedicated therapies, such as immune checkpoint inhibitors or targeted therapies, in both human and veterinary medicine. Mucosal melanoma (MM) is a rare and aggressive clinical cancer. Despite recent advances in genetics and treatment, the prognosis of MM remains poor. Canine MM provides a relevant spontaneous and immunocompetent model to decipher the genetic basis and explore treatments for MM. We performed an integrative genomic and transcriptomic analysis of 32 canine MM samples, which identified two molecular subgroups with different microenvironment and structural variant (SV) content. Overexpression of genes related to the microenvironment and T-cell response was associated with tumors with lower SV content, whereas overexpression of pigmentation-related pathways and oncogenes, such as TERT, was associated with high SV load. Using whole genome sequencing, we showed that focal amplifications characterized complex chromosomal rearrangements targeting oncogenes, such as MDM2 or CDK4, and a recurrently amplified region on canine chromosome 30. We also demonstrated that the genes TRPM7, GABPB1, and SPPL2A, located in this CFA30 region, play a role in cell proliferation, and thus can be considered as novel candidate oncogenes for human MM. Our results suggest the existence of two molecular subgroups of MM that could benefit from specific therapies, such as immune checkpoint inhibitors or targeted therapies, in both human and veterinary medicine.


  • Anaïs Prouteau

See also

Prouteau, A.; Mottier, S.; Primot, A.; Cadieu, E.; Bachelot, L.; Botherel, N.; Cabillic, F.; Houel, A.; Cornevin, L.; Kergal, C.; Corre, S.; Abadie, J.; Hitte, C.; Gilot, D.; Lindblad-Toh, K.; André, C.; Derrien, T.; Hedan, B. Canine Oral Melanoma Genomic and Transcriptomic Study Defines Two Molecular Subgroups with Different Therapeutical Targets. Cancers 2022, 14, 276.