QIMR Berghofer

Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity.

Abstract

To increase understanding of the genomic landscape of acral melanoma, a rare form of melanoma occurring on palms, soles or nail beds, whole genome sequencing of 87 tumors with matching transcriptome sequencing for 63 tumors was performed. Here we report that mutational signature analysis reveals a subset of tumors, mostly subungual, with an ultraviolet radiation signature. Significantly mutated genes are BRAF, NRAS, NF1, NOTCH2, PTEN and TYRP1. Mutations and amplification of KIT are also common. Structural rearrangement and copy number signatures show that whole genome duplication, aneuploidy and complex rearrangements are common. Complex rearrangements occur recurrently and are associated with amplification of TERT, CDK4, MDM2, CCND1, PAK1 and GAB2, indicating potential therapeutic options.

Authors Newell, Felicity; Wilmott, James S; Johansson, Peter A; Nones, Katia; Addala, Venkateswar; Mukhopadhyay, Pamela; Broit, Natasa; Amato, Carol M; Van Gulick, Robert; Kazakoff, Stephen H; Patch, Ann-Marie; Koufariotis, Lambros T; Lakis, Vanessa; Leonard, Conrad; Wood, Scott; Holmes, Oliver; Xu, Qinying; Lewis, Karl; Medina, Theresa; Gonzalez, Rene; Saw, Robyn P M; Spillane, Andrew J; Stretch, Jonathan R; Rawson, Robert V; Ferguson, Peter M; Dodds, Tristan J; Thompson, John F; Long, Georgina V; Levesque, Mitchell P; Robinson, William A; Pearson, John V; Mann, Graham J; Scolyer, Richard A; Waddell, Nicola; Hayward, Nicholas K
Journal Nature Communications
Pages 5259
Volume 11
Date 1/10/2020
Grant ID 1093017
Funding Body National Health and Medical Research Council of Australia (NHMRC) Program Grant
URL http://www.ncbi.nlm.nih.gov/pubmed/?term=10.1038/s41467-020-18988-3
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