Back to Search Start Over

Whole genome landscapes of uveal melanoma show an ultraviolet radiation signature in iris tumours

Authors :
Johansson, Peter A.
Brooks, Kelly
Newell, Felicity
Palmer, Jane M.
Wilmott, James S.
Pritchard, Antonia L.
Broit, Natasa
Wood, Scott
Carlino, Matteo S.
Leonard, Conrad
Koufariotis, Labros T.
Nathan, Vaishnavi
Beasley, Aaron B.
Howlie, Madeleine
Dawson, Rebecca
Rizos, Helen
Schmidt, Chris W.
Long, Georgina V.
Hamilton, Hayley
Kiilgaard, Jens F.
Isaacs, Timothy
Gray, Elin S.
Rolfe, Olivia J.
Park, John J.
Stark, Andrew
Mann, Graham J.
Scolyer, Richard A.
Pearson, John V.
van Baren, Nicolas
Waddell, Nicola
Wadt, Karin W.
McGrath, Lindsay A.
Warrier, Sunil K.
Glasson, William
Hayward, Nicholas K.
Johansson, Peter A.
Brooks, Kelly
Newell, Felicity
Palmer, Jane M.
Wilmott, James S.
Pritchard, Antonia L.
Broit, Natasa
Wood, Scott
Carlino, Matteo S.
Leonard, Conrad
Koufariotis, Labros T.
Nathan, Vaishnavi
Beasley, Aaron B.
Howlie, Madeleine
Dawson, Rebecca
Rizos, Helen
Schmidt, Chris W.
Long, Georgina V.
Hamilton, Hayley
Kiilgaard, Jens F.
Isaacs, Timothy
Gray, Elin S.
Rolfe, Olivia J.
Park, John J.
Stark, Andrew
Mann, Graham J.
Scolyer, Richard A.
Pearson, John V.
van Baren, Nicolas
Waddell, Nicola
Wadt, Karin W.
McGrath, Lindsay A.
Warrier, Sunil K.
Glasson, William
Hayward, Nicholas K.
Source :
Research outputs 2014 to 2021
Publication Year :
2020

Abstract

Uveal melanoma (UM) is the most common intraocular tumour in adults and despite surgical or radiation treatment of primary tumours, ~50% of patients progress to metastatic disease. Therapeutic options for metastatic UM are limited, with clinical trials having little impact. Here we perform whole-genome sequencing (WGS) of 103 UM from all sites of the uveal tract (choroid, ciliary body, iris). While most UM have low tumour mutation burden (TMB), two subsets with high TMB are seen; one driven by germline MBD4 mutation, and another by ultraviolet radiation (UVR) exposure, which is restricted to iris UM. All but one tumour have a known UM driver gene mutation (GNAQ, GNA11, BAP1, PLCB4, CYSLTR2, SF3B1, EIF1AX). We identify three other significantly mutated genes (TP53, RPL5 and CENPE).

Details

Database :
OAIster
Journal :
Research outputs 2014 to 2021
Notes :
application/pdf, Research outputs 2014 to 2021
Publication Type :
Electronic Resource
Accession number :
edsoai.on1366597303
Document Type :
Electronic Resource