학술논문

Integrative Molecular Characterization of Malignant Pleural Mesothelioma
Document Type
article
Author
Hmeljak, JulijaSanchez-Vega, FranciscoHoadley, Katherine AShih, JuliannStewart, ChipHeiman, DavidTarpey, PatrickDanilova, LudmilaDrill, EstherGibb, Ewan ABowlby, ReanneKanchi, RupaOsmanbeyoglu, Hatice USekido, YoshitakaTakeshita, JumpeiNewton, YuliaGraim, KileyGupta, ManaswiGay, Carl MDiao, LixiaGibbs, David LThorsson, VesteinnIype, LisaKantheti, HavishSeverson, David TRavegnini, GloriaDesmeules, PatriceJungbluth, Achim ATravis, William DDacic, SanjaChirieac, Lucian RGalateau-Sallé, FrançoiseFujimoto, JunyaHusain, Aliya NSilveira, Henrique CRusch, Valerie WRintoul, Robert CPass, HarveyKindler, HedyZauderer, Marjorie GKwiatkowski, David JBueno, RaphaelTsao, Anne SCreaney, JenetteLichtenberg, TaraLeraas, KristenBowen, JayFelau, InaZenklusen, Jean ClaudeAkbani, RehanCherniack, Andrew DByers, Lauren ANoble, Michael SFletcher, Jonathan ARobertson, A GordonShen, RonglaiAburatani, HiroyukiRobinson, Bruce WCampbell, PeterLadanyi, MarcAlly, AdrianAnur, PavanaArmenia, JoshuaAuman, J ToddBalasundaram, MirunaBalu, SaianandBaylin, Stephen BBecich, MichaelBehrens, CarmenBeroukhim, RameenBielski, CraigBodenheimer, TomBootwalla, Moiz SBrooks, DeniseByers, Lauren AverettCárcano, Flávio MCarlsen, RebeccaCarvalho, Andre LCheung, DorothyChirieac, LucianCho, JuokChuah, EricChudamani, SudhaCibulskis, CarrieCope, LeslieCrain, DanielCurley, ErinRienzo, Assunta DeDeFreitas, TimothyDemchok, John ADhalla, Noreen
Source
Cancer Discovery. 8(12)
Subject
Rare Diseases
Lung Cancer
Biotechnology
Lung
Cancer
Human Genome
Genetics
2.1 Biological and endogenous factors
Aetiology
Good Health and Well Being
Aged
Biomarkers
Tumor
Female
Histone-Lysine N-Methyltransferase
Humans
Kaplan-Meier Estimate
Lung Neoplasms
Male
Mesothelioma
Middle Aged
Mutation
Pleural Neoplasms
Prognosis
Protein Methyltransferases
Tumor Suppressor Proteins
Ubiquitin Thiolesterase
TCGA Research Network
Oncology and Carcinogenesis
Language
Abstract
Malignant pleural mesothelioma (MPM) is a highly lethal cancer of the lining of the chest cavity. To expand our understanding of MPM, we conducted a comprehensive integrated genomic study, including the most detailed analysis of BAP1 alterations to date. We identified histology-independent molecular prognostic subsets, and defined a novel genomic subtype with TP53 and SETDB1 mutations and extensive loss of heterozygosity. We also report strong expression of the immune-checkpoint gene VISTA in epithelioid MPM, strikingly higher than in other solid cancers, with implications for the immune response to MPM and for its immunotherapy. Our findings highlight new avenues for further investigation of MPM biology and novel therapeutic options. SIGNIFICANCE: Through a comprehensive integrated genomic study of 74 MPMs, we provide a deeper understanding of histology-independent determinants of aggressive behavior, define a novel genomic subtype with TP53 and SETDB1 mutations and extensive loss of heterozygosity, and discovered strong expression of the immune-checkpoint gene VISTA in epithelioid MPM.See related commentary by Aggarwal and Albelda, p. 1508.This article is highlighted in the In This Issue feature, p. 1494.