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. 2012 May 6;44(6):651-8.
doi: 10.1038/ng.2270.

Detectable clonal mosaicism and its relationship to aging and cancer

Kevin B Jacobs  1 Meredith YeagerWeiyin ZhouSholom WacholderZhaoming WangBenjamin Rodriguez-SantiagoAmy HutchinsonXiang DengChenwei LiuMarie-Josephe HornerMichael CullenCaroline G EpsteinLaurie BurdettMichael C DeanNilanjan ChatterjeeJoshua SampsonCharles C ChungJoseph KovaksSusan M GapsturVictoria L StevensLauren T TerasMia M GaudetDemetrius AlbanesStephanie J WeinsteinJarmo VirtamoPhilip R TaylorNeal D FreedmanChristian C AbnetAlisa M GoldsteinNan HuKai YuJian-Min YuanLinda LiaoTi DingYou-Lin QiaoYu-Tang GaoWoon-Puay KohYong-Bing XiangZe-Zhong TangJin-Hu FanMelinda C AldrichChristopher AmosWilliam J BlotCathryn H BockElizabeth M GillandersCurtis C HarrisChristopher A HaimanBrian E HendersonLaurence N KolonelLoic Le MarchandLorna H McNeillBenjamin A RybickiAnn G SchwartzLisa B SignorelloMargaret R SpitzJohn K WienckeMargaret WrenschXifeng WuKrista A ZanettiRegina G ZieglerJonine D FigueroaMontserrat Garcia-ClosasNuria MalatsGaelle MarenneLudmila Prokunina-OlssonDalsu BarisMolly SchwennAlison JohnsonMaria Teresa LandiLynn GoldinDario ConsonniPier Alberto BertazziMelissa RotunnoPreetha RajaramanUlrika AnderssonLaura E Beane FreemanChristine D BergJulie E BuringMary A ButlerTania CarreonMaria FeychtingAnders AhlbomJ Michael GazianoGraham G GilesGoran HallmansSusan E HankinsonPatricia HartgeRoger HenrikssonPeter D InskipChristoffer JohansenAnnelie LandgrenRoberta McKean-CowdinDominique S MichaudBeatrice S MelinUlrike PetersAvima M RuderHoward D SessoGianluca SeveriXiao-Ou ShuKala VisvanathanEmily WhiteAlicja WolkAnne Zeleniuch-JacquotteWei ZhengDebra T SilvermanManolis KogevinasJuan R GonzalezOlaya VillaDonghui LiEric J DuellHarvey A RischSara H OlsonCharles KooperbergBrian M WolpinLi JiaoManal HassanWilliam WheelerAlan A ArslanH Bas Bueno-de-MesquitaCharles S FuchsSteven GallingerMyron D GrossElizabeth A HollyAlison P KleinAndrea LaCroixMargaret T MandelsonGloria PetersenMarie-Christine Boutron-RuaultPaige M BracciFederico CanzianKenneth ChangMichelle CotterchioEdward L GiovannucciMichael GogginsJudith A Hoffman BoltonMazda JenabKay-Tee KhawVittorio KroghRobert C KurtzRobert R McWilliamsJulie B MendelsohnKari G RabeElio RiboliAnne TjønnelandGeoffrey S TobiasDimitrios TrichopoulosJoanne W ElenaHerbert YuLaufey AmundadottirRachael Z Stolzenberg-SolomonPeter KraftFredrick SchumacherDaniel StramSharon A SavageLisa MirabelloIrene L AndrulisJay S WunderAna Patiño GarcíaLuis SierrasesúmagaDonald A BarkauskasRichard G GorlickMark PurdueWong-Ho ChowLee E MooreKendra L SchwartzFaith G DavisAnn W HsingSonja I BerndtAmanda BlackNicolas WentzensenLouise A BrintonJolanta LissowskaBeata PeplonskaKatherine A McGlynnMichael B CookBarry I GraubardChristian P KratzMark H GreeneRalph L EricksonDavid J HunterGilles ThomasRobert N HooverFrancisco X RealJoseph F Fraumeni JrNeil E CaporasoMargaret TuckerNathaniel RothmanLuis A Pérez-JuradoStephen J Chanock
Affiliations

Detectable clonal mosaicism and its relationship to aging and cancer

Kevin B Jacobs et al. Nat Genet. .

Abstract

In an analysis of 31,717 cancer cases and 26,136 cancer-free controls from 13 genome-wide association studies, we observed large chromosomal abnormalities in a subset of clones in DNA obtained from blood or buccal samples. We observed mosaic abnormalities, either aneuploidy or copy-neutral loss of heterozygosity, of >2 Mb in size in autosomes of 517 individuals (0.89%), with abnormal cell proportions of between 7% and 95%. In cancer-free individuals, frequency increased with age, from 0.23% under 50 years to 1.91% between 75 and 79 years (P = 4.8 × 10(-8)). Mosaic abnormalities were more frequent in individuals with solid tumors (0.97% versus 0.74% in cancer-free individuals; odds ratio (OR) = 1.25; P = 0.016), with stronger association with cases who had DNA collected before diagnosis or treatment (OR = 1.45; P = 0.0005). Detectable mosaicism was also more common in individuals for whom DNA was collected at least 1 year before diagnosis with leukemia compared to cancer-free individuals (OR = 35.4; P = 3.8 × 10(-11)). These findings underscore the time-dependent nature of somatic events in the etiology of cancer and potentially other late-onset diseases.

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Figures

Figure 1
Figure 1. Characteristics of detectable clonal mosaic events
Detectable clonal mosaic events plotted by proportion of abnormal cells (p) and Log R Ratio (LRR) for 681 events in 517 individuals.
Figure 2
Figure 2. Circular genomic plot of detectable clonal mosaic events
Genomic location of detectable clonal mosaic events. Outer rings are the autosomes 1 to 22. Yellow region denotes events of copy neutral loss of heterozygosity. Blue region denotes copy gain events. Red region denotes copy loss events. Panel A includes events in cancer free controls. Panel B includes events in cancer cases.
Figure 3
Figure 3. Frequency of detectable clonal mosaic events by age and cancer status
Analysis excluded 1,000 individuals with unknown age at DNA collection. 95% confidence intervals are shown.

Comment in

  • Exploring the variation within.
    Macosko EZ, McCarroll SA. Macosko EZ, et al. Nat Genet. 2012 May 29;44(6):614-6. doi: 10.1038/ng.2311. Nat Genet. 2012. PMID: 22641203

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