An Analysis of Growth, Differentiation and Apoptosis Genes with Risk of Renal Cancer 英文参考文献.docVIP
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An Analysis of Growth, Differentiation and Apoptosis Genes with Risk of Renal Cancer 英文参考文献
AnAnalysisofGrowth,DifferentiationandApoptosis
GeneswithRiskofRenalCancer
LindaM.Dong1*,PaulBrennan2,SaraKarami1,RayjeanJ.Hung3,IdanMenashe1,SonjaI.Berndt1,
MeredithYeager4,StephenChanock4,DavidZaridze5,VsevolodMatveev5,VladimirJanout6 ,Hellena
Kollarova6,VladimirBencko7,KendraSchwartz8,FaithDavis9,MarieNavratilova10,NeonilaSzeszenia-
Dabrowska11,DanaMates12,JoanneS.Colt1,IvanaHolcatova7,PaoloBoffetta3,NathanielRothman1,
Wong-HoChow1,PhilipS.Rosenberg1,LeeE.Moore1
1DivisionofCancerEpidemiologyandGenetics,NationalCancerInstitute,Bethesda,Maryland,UnitedStatesofAmerica,2InternationalAgencyforResearchonCancer,
Lyon, France, 3Samuel Lunenfeld Research Institute of Mount Sinai Hospital, Toronto, Canada, 4Core Genotyping Facility, National Cancer Institute, Gaithersberg,
Maryland, United States of America, 5Institute of Carcinogenesis, Moscow, Russia, 6Palacky University, Olomouc, Czech Republic, 7Institute of Hygiene and
Epidemiology, Prague, Czech Republic, 8Department of Family Medicine and Public Health Sciences and Karmanos Cancer Institute, Wayne State University, Detroit,
Michigan, United States of America, 9Department of Biostatistics and Epidemiology, University of Illinois at Chicago, Chicago, Illinois, United States of America,
10MasarykMemorialCancerInstitute,Brno,CzechRepublic,11InstituteofOccupationalMedicine,Lodz,Poland,12InstitueofPublicHealth,Bucharest,Romania
Abstract
We conducted a case-control study of renal cancer (987 cases and 1298 controls) in Central and Eastern Europe and
analyzedgenomicDNAfor319taggingsingle-nucleotidepolymorphisms(SNPs)in21genesinvolvedincellulargrowth,
differentiationandapoptosisusinganIlluminaOligoPoolAll(OPA).Ahaplotype-basedmethod(slidingwindowanalysisof
consecutiveSNPs)wasusedtoidentifychromosomeregionsofinterestthatremainedsignificantatafalsediscoveryrateof
10%. Subsequently, risk estimates were generated for regions with a high level of signal and individual SNPs by
unconditional logistic regression adjusting for age,
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