The Genetic Evolution of Melanoma from Precursor Lesions

被引:740
作者
Shain, A. Hunter [1 ,2 ,3 ]
Yeh, Iwei [1 ,2 ,3 ]
Kovalyshyn, Ivanka [4 ,5 ]
Sriharan, Aravindhan [6 ]
Talevich, Eric [1 ,2 ,3 ]
Gagnon, Alexander [1 ,2 ,3 ]
Dummer, Reinhard [7 ]
North, Jeffrey [1 ,2 ]
Pincus, Laura [1 ,2 ]
Ruben, Beth [1 ,2 ]
Rickaby, William [9 ]
D'Arrigo, Corrado [8 ]
Robson, Alistair [9 ]
Bastian, Boris C. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[4] Cleveland Clin, Dept Dermatol, Cleveland, OH 44195 USA
[5] Cleveland Clin, Dept Pathol, Cleveland, OH 44195 USA
[6] Orlando Hlth, Dept Pathol, Orlando, FL USA
[7] Univ Zurich Hosp, Dept Dermatol, CH-8091 Zurich, Switzerland
[8] Dorset Cty Hosp, Dept Dermatol, Dorchester, Dorset, England
[9] St Johns Inst Dermatol, Dept Dermatol, London, England
基金
美国国家卫生研究院;
关键词
DYSPLASTIC NEVUS SYNDROME; TERT PROMOTER MUTATIONS; SOMATIC MUTATIONS; UVEAL MELANOMA; BRAF MUTATIONS; RECURRENT; TISSUES; NUMBER; SF3B1; RISK;
D O I
10.1056/NEJMoa1502583
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND The pathogenic mutations in melanoma have been largely catalogued; however, the order of their occurrence is not known. METHODS We sequenced 293 cancer-relevant genes in 150 areas of 37 primary melanomas and their adjacent precursor lesions. The histopathological spectrum of these areas included unequivocally benign lesions, intermediate lesions, and intraepidermal or invasive melanomas. RESULTS Precursor lesions were initiated by mutations of genes that are known to activate the mitogen-activated protein kinase pathway. Unequivocally benign lesions harbored BRAF V600E mutations exclusively, whereas those categorized as intermediate were enriched for NRAS mutations and additional driver mutations. A total of 77% of areas of intermediate lesions and melanomas in situ harbored TERT promoter mutations, a finding that indicates that these mutations are selected at an unexpectedly early stage of the neoplastic progression. Biallelic inactivation of CDKN2A emerged exclusively in invasive melanomas. PTEN and TP53 mutations were found only in advanced primary melanomas. The point-mutation burden increased from benign through intermediate lesions to melanoma, with a strong signature of the effects of ultraviolet radiation detectable at all evolutionary stages. Copy-number alterations became prevalent only in invasive melanomas. Tumor heterogeneity became apparent in the form of genetically distinct subpopulations as melanomas progressed. CONCLUSIONS Our study defined the succession of genetic alterations during melanoma progression, showing distinct evolutionary trajectories for different melanoma subtypes. It identified an intermediate category of melanocytic neoplasia, characterized by the presence of more than one pathogenic genetic alteration and distinctive histopathological features. Finally, our study implicated ultraviolet radiation as a major factor in both the initiation and progression of melanoma. (Funded by the National Institutes of Health and others.)
引用
收藏
页码:1926 / 1936
页数:11
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