Distinct genomic features in a retrospective cohort of mucosal, acral, and vulvovaginal melanomas

• Published in: Journal of the American Academy of Dermatology 2023-05, Vol.88 (5), p.1051-1059
• Main Authors: Shi, Katherine, Zhang, Bin, Kong, Betty Y., Zhang, Yongzhan, Igartua, Catherine, Mohan, Lauren S., Quan, Victor L., Panah, Elnaz, Isales, Maria Cristina, Beaubier, Nike, Taxter, Timothy J., White, Kevin P., Zou, Lihua, Gerami, Pedram
• Format: Article
• Language: English
• Subjects: acral; AURKA; BRAF; CDKN2A; cell cycle and proliferation; CNV; DNA; ERBB2; expression; genomic; Genomics; head and neck; HER2/Neu; Humans; melanoma; Melanoma - pathology; Melanoma, Cutaneous Malignant; mRNA; mucosal; Mutation; NF1; NRAS; Retrospective Studies; sequencing; Skin Neoplasms - pathology; sun-exposed; sun-protected; TERT; TMB; ultraviolet; Ultraviolet Rays - adverse effects; vaginal; vulvar; vulvovaginal
• ISSN: 0190-9622; 1097-6787
• DOI: 10.1016/j.jaad.2019.07.017

Compared with sun-exposed melanomas, less is known regarding the pathogenesis of sun-protected melanomas. Sun-protected melanomas share many epidemiologic factors, but their genetic heterogeneity is not well studied. We investigated the genomic profile of acral, mucosal, and vulvovaginal melanomas. We hypothesize that mucosal melanomas, recognized for their uniquely aggressive clinical behavior, have distinct genomic features. We performed whole transcriptome messenger RNA and DNA (1711 genes) sequencing, messenger RNA expression profiling, tumor mutational burden, ultraviolet signature, and copy number variants analysis on 29 volar/digital acral, 7 mucosal, and 6 vulvovaginal melanomas. There was significant genetic heterogeneity, particularly in acral melanomas, with 36% having BRAF alterations, whereas other melanomas had none (P = .0159). Nonzero ultraviolet signatures were more frequent in acral melanomas, suggesting greater ultraviolet involvement. Mucosal melanomas formed a distinct group with increased expression of cell cycle and proliferation genes. Various targetable aberrations were identified, such as AURKA and ERBB2, in mucosal and acral melanomas, respectively. The sample size was a small. There is significant genetic heterogeneity among sun-protected melanomas. Mucosal melanomas have upregulation in cell cycle and proliferation genes, which may explain their aggressive behavior. Ultraviolet radiation plays some role in a subset of acral but not other melanomas.