학술논문

Cross-species genomic landscape comparison of human mucosal melanoma with canine oral and equine melanoma.
Document Type
article
Source
Nature communications. 10(1)
Subject
Mucous Membrane
Animals
Dogs
Horses
Humans
Melanoma
Mouth Neoplasms
Skin Neoplasms
Neoplasm Recurrence
Local
GTP Phosphohydrolases
Protein-Serine-Threonine Kinases
Cell Cycle Proteins
Microtubule-Associated Proteins
Cadherins
Membrane Proteins
Neoplasm Proteins
Tumor Suppressor Proteins
BRCA1 Protein
BRCA2 Protein
Species Specificity
Gene Expression Regulation
Neoplastic
Germ-Line Mutation
Tumor Suppressor Protein p53
PTEN Phosphohydrolase
Proto-Oncogene Proteins c-mdm2
Receptor-Like Protein Tyrosine Phosphatases
Class 3
DNA Copy Number Variations
Carcinogenesis
Gene Expression Regulation
Neoplastic
Neoplasm Recurrence
Local
Receptor-Like Protein Tyrosine Phosphatases
Class 3
Language
Abstract
Mucosal melanoma is a rare and poorly characterized subtype of human melanoma. Here we perform a cross-species analysis by sequencing tumor-germline pairs from 46 primary human muscosal, 65 primary canine oral and 28 primary equine melanoma cases from mucosal sites. Analysis of these data reveals recurrently mutated driver genes shared between species such as NRAS, FAT4, PTPRJ, TP53 and PTEN, and pathogenic germline alleles of BRCA1, BRCA2 and TP53. We identify a UV mutation signature in a small number of samples, including human cases from the lip and nasal mucosa. A cross-species comparative analysis of recurrent copy number alterations identifies several candidate drivers including MDM2, B2M, KNSTRN and BUB1B. Comparison of somatic mutations in recurrences and metastases to those in the primary tumor suggests pervasive intra-tumor heterogeneity. Collectively, these studies suggest a convergence of some genetic changes in mucosal melanomas between species but also distinctly different paths to tumorigenesis.