The genetic evolution of metastatic uveal melanoma

被引:132
|
作者
Shain, A. Hunter [1 ,2 ]
Bagger, Mette M. [3 ,4 ]
Yu, Richard [1 ,2 ]
Chang, Darwin [1 ,2 ]
Liu, Shanshan [1 ,2 ]
Vemula, Swapna [5 ]
Weier, Jingly F. [5 ]
Wadt, Karin [4 ]
Heegaard, Steffen [3 ,6 ]
Bastian, Boris C. [1 ,2 ,5 ]
Kiilgaard, Jens F. [3 ]
机构
[1] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[3] Copenhagen Univ Hosp, Rigshosp, Dept Ophthalmol, Copenhagen, Denmark
[4] Copenhagen Univ Hosp, Rigshosp, Dept Clin Genet, Copenhagen, Denmark
[5] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA
[6] Copenhagen Univ Hosp, Rigshosp, Dept Pathol, Copenhagen, Denmark
关键词
DEPENDENT PROBE AMPLIFICATION; ACTIVATING MUTATIONS; SOMATIC MUTATIONS; GNAQ; BAP1; HETEROGENEITY; SF3B1;
D O I
10.1038/s41588-019-0440-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Uveal melanoma is a clinically distinct and particularly lethal subtype of melanoma originating from melanocytes in the eye. Here, we performed multi-region DNA sequencing of primary uveal melanomas and their matched metastases from 35 patients. We observed previously unknown driver mutations and established the order in which these and known driver mutations undergo selection. Metastases had genomic alterations distinct from their primary tumors; metastatic dissemination sometimes occurred early during the development of the primary tumor. Our study offers new insights into the genetics and evolution of this melanoma subtype, providing potential biomarkers for progression and therapy.
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页码:1123 / +
页数:10
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