Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma

被引:5
|
作者
Birkealv, Sofia [1 ]
Harland, Mark [2 ]
Matsuyama, Larissa Satiko Alcantara Sekimoto [1 ,3 ]
Rashid, Mamun [1 ]
Mehta, Ishan [1 ]
Laye, Jonathan P. [2 ]
Haase, Kerstin [4 ]
Mell, Tracey [2 ]
Iyer, Vivek [1 ]
Robles-Espinoza, Carla Daniela [1 ,5 ]
McDermott, Ultan [1 ]
van Loo, Peter [4 ]
Kuijjer, Marieke L. [6 ,7 ,8 ]
Possik, Patricia A. [9 ]
Engler, Silvya Stuchi Maria [3 ]
Bishop, D. Timothy [2 ]
Newton-Bishop, Julia [2 ]
Adams, David J. [1 ]
机构
[1] Wellcome Sanger Inst, Wellcome Trust Genome Campus, Cambridge, England
[2] Univ Leeds, Div Haematol & Immunol, Sch Med, Leeds, W Yorkshire, England
[3] Univ Sao Paulo, Sch Pharmaceut Sci, Dept Clin & Toxicol Anal, Sao Paulo, Brazil
[4] Francis Crick Inst, London, England
[5] Univ Nacl Autonoma Mexico, Lab Int Invest Genoma Humano, Campus Juriquilla, Santiago De Queretaro, Mexico
[6] Univ Oslo, Fac Med, Ctr Mol Med Norway NCMM, Nordic EMBL Partnership, Oslo, Norway
[7] Leiden Univ, Dept Pathol, Med Ctr, Leiden, Netherlands
[8] Leiden Univ, Leiden Ctr Computat Oncol, Med Ctr, Leiden, Netherlands
[9] Brazilian Natl Canc Inst, Div Expt & Translat Res, Rio De Janeiro, Brazil
来源
JOURNAL OF PATHOLOGY | 2023年 / 259卷 / 01期
基金
英国惠康基金; 欧洲研究理事会; 英国医学研究理事会;
关键词
melanoma; gene essentiality; genetic epistasis; genomic landscape; CRISPR screening; interferon regulatory factor 4 (IRF4); genome sequencing; somatic mutation; driver genes; primary cancer; PROMOTER MUTATIONS; CANCER; PROTEIN; PATTERNS; BINDING; COPY; SKIN;
D O I
10.1002/path.6019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Melanoma is a heterogenous malignancy with an unpredictable clinical course. Most patients who present in the clinic are diagnosed with primary melanoma, yet large-scale sequencing efforts have focused primarily on metastatic disease. In this study we sequence-profiled 524 American Joint Committee on Cancer Stage I-III primary tumours. Our analysis of these data reveals recurrent driver mutations, mutually exclusive genetic interactions, where two genes were never or rarely co-mutated, and an absence of co-occurring genetic events. Further, we intersected copy number calls from our primary melanoma data with whole-genome CRISPR screening data to identify the transcription factor interferon regulatory factor 4 (IRF4) as a melanoma-associated dependency. (c) 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
引用
收藏
页码:56 / 68
页数:13
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