Evolution of late-stage metastatic melanoma is dominated by aneuploidy and whole genome doubling.
Ontology highlight
ABSTRACT: Although melanoma is initiated by acquisition of point mutations and limited focal copy number alterations in melanocytes-of-origin, the nature of genetic changes that characterise lethal metastatic disease is poorly understood. Here, we analyze the evolution of human melanoma progressing from early to late disease in 13 patients by sampling their tumours at multiple sites and times. Whole exome and genome sequencing data from 88 tumour samples reveals only limited gain of point mutations generally, with net mutational loss in some metastases. In contrast, melanoma evolution is dominated by whole genome doubling and large-scale aneuploidy, in which widespread loss of heterozygosity sculpts the burden of point mutations, neoantigens and structural variants even in treatment-naïve and primar
SUBMITTER: Vergara IA
PROVIDER: S-EPMC7933255 | biostudies-literature | 2021 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA