Dysfunctions Associated with Methylation, MicroRNA Expression and Gene Expression in Lung Cancer 英文参考文献.docVIP
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Dysfunctions Associated with Methylation, MicroRNA Expression and Gene Expression in Lung Cancer 英文参考文献
DysfunctionsAssociatedwithMethylation,MicroRNA
ExpressionandGeneExpressioninLungCancer
TaoHuang2,3¤,MinJiang4,5,XiangyinKong4,5*,Yu-DongCai1*
1InstituteofSystemsBiology,ShanghaiUniversity,Shanghai,People’sRepublicofChina,2KeyLaboratoryofSystemsBiology,ShanghaiInstitutesforBiologicalSciences,
ChineseAcademyofSciences,Shanghai,People’sRepublicofChina,3ShanghaiCenterforBioinformationTechnology,Shanghai,People’sRepublicofChina,4Instituteof
Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai, People’s
RepublicofChina,5StateKeyLaboratoryofMedicalGenomics,RuijinHospital,ShanghaiJiaotongUniversity,Shanghai,People’sRepublicofChina
Abstract
Integratinghigh-throughputdataobtainedfromdifferentmolecularlevelsisessentialforunderstandingthemechanismsof
complexdiseasessuchascancer.Inthisstudy,weintegratedthemethylation,microRNAandmRNAdatafromlungcancer
tissuesandnormallungtissuesusingfunctionalgenesets.ForeachGeneOntology(GO)term,threesetsweredefined:the
methylationset,themicroRNAsetandthemRNAset.Thediscriminatingabilityofeachgenesetwasrepresentedbythe
Matthews correlation coefficient (MCC), as evaluated by leave-one-out cross-validation (LOOCV). Next, the MCCs in the
methylation sets, the microRNA sets and the mRNA sets were ranked. By comparing the MCC ranks of methylation,
microRNA and mRNA for each GO term, we classified the GO sets into six groups and identified the dysfunctional
methylation, microRNA and mRNA gene sets in lung cancer. Our results provide a systematic view of the functional
alterations during tumorigenesis that may help to elucidate the mechanisms of lung cancer and lead to improved
treatmentsforpatients.
Citation:HuangT,JiangM,KongX,CaiY-D(2012)DysfunctionsAssociatedwithMethylation,MicroRNAExpressionandGeneExpressioninLungCancer.PLoS
ONE7(8):e43441.doi:10.1371/journal.pone.0043441
Editor:DaotaiNie,SouthernIllinoisUniversitySchoolofMedicine,UnitedStatesofAmer
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