The mutational landscape of mucosal melanoma

被引:114
|
作者
Nassar, Kelsey W. [1 ,2 ]
Tan, Aik Choon [1 ,2 ,3 ]
机构
[1] Univ Colorado, Sch Med, Dept Med, Div Med Oncol, Anschutz Med Campus, Aurora, CO 80111 USA
[2] Univ Colorado, Canc Biol Training Program, Grad Sch, Anschutz Med Campus, Aurora, CO 80111 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Dept Biostat & Bioinformat, 12902 Magnolia Dr, Tampa, FL 33612 USA
基金
美国国家卫生研究院;
关键词
Mucosal melanoma; KIT; SF3B1; Mutational landscape; Druggable targets; KIT PROTEIN EXPRESSION; C-KIT; NRAS MUTATIONS; PHASE-II; GENE-MUTATIONS; BRAF MUTATIONS; METASTATIC MELANOMA; ONCOGENIC MUTATIONS; THERAPEUTIC TARGET; MALIGNANT-MELANOMA;
D O I
10.1016/j.semcancer.2019.09.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mucosal melanoma is a rare and aggressive subtype of melanoma that has a less favorable prognosis due to the lack of understanding and identification of oncogenic drivers. Recently, whole genome and whole exome sequencing have unveiled the molecular landscape and potential oncogenic drivers of mucosal melanoma, which remains distinct from cutaneous melanoma. In this review, we provide an overview of the genomic landscape of mucosal melanoma, with a focus on molecular studies identifying potential oncogenic drivers allowing for a better mechanistic understanding of the biology of mucosal melanoma. We summarized the published genomics and clinical data supporting the observations that mucosal melanoma harbors distinct genetic alterations and oncogenic drivers from cutaneous melanoma, and thus should be treated accordingly. The common drivers (BRAF and NRAS) found in cutaneous melanoma have lower mutation rate in mucosal melanoma. In contrast, SF3B1 and KIT have higher mutation rate in mucosal melanoma as compared to cutaneous melanoma. From the meta-analysis, we also observed that the mutational profiles are slightly different between the "upper" and "lower" regions of mucosal melanoma, providing new insights and therapeutic options for the mucosal melanoma patients. Mutations identified in mucosal melanoma should be incorporated into routine clinical testing, as there are targeted therapies already developed for treating patients with these mutations in the precision medicine era.
引用
收藏
页码:139 / 148
页数:10
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