Evaluation of the Psoriasis Transcriptome across Different Studies by Gene Set Enrichment Analysis (GSEA) 英文参考文献.docVIP
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Evaluation of the Psoriasis Transcriptome across Different Studies by Gene Set Enrichment Analysis (GSEA) 英文参考文献
EvaluationofthePsoriasisTranscriptomeacross
DifferentStudiesbyGeneSetEnrichmentAnalysis
(GSEA)
MayteSua′rez-Farin?as1,2,MichelleA.Lowes1,LisaC.Zaba1,JamesG.Krueger1*
1LaboratoryforInvestigativeDermatology,TheRockefellerUniversity,NewYork,NewYork,UnitedStatesofAmerica,2CenterforClinicalandTranslationalScience,The
RockefellerUniversity,NewYork,NewYork,UnitedStatesofAmerica
Abstract
Background:Ourobjectivewastodevelopaconsistentmoleculardefinitionofpsoriasis.Therehavebeenseveralpublished
microarraystudiesofpsoriasis,andwecompareddisease-relatedgenesidentifiedacrossthesedifferentstudiesofpsoriasis
withourowninordertoestablishaconsensus.
Methodology/PrincipalFindings:Wepresentapsoriasistranscriptomefromagroupof15patientsenrolledinaclinical
study, and assessed its biological validity using a set of important pathways known to be involved in psoriasis. We also
identifiedakeysetofcytokinesthatarenowstronglyimplicatedindrivingdisease-relatedpathology,butwhicharenot
detected well on gene array platforms and require more sensitive methods to measure mRNA levels in skin tissues.
Comparisonofourtranscriptomewiththreeotherpublishedlistsofpsoriasisgenesshowedapparentinconsistenciesbased
onthenumberofoverlappinggenes.Weextendedthewell-establishedapproachofGeneSetEnrichmentAnalysis(GSEA)
tocompareanewstudywiththeseotherpublishedlistofdifferentiallyexpressedgenes(DEG)inamorecomprehensive
manner. We applied our method to these three published psoriasis transcriptomes and found them to be in good
agreementwithourstudy.
Conclusions/Significance:Duetowidevariabilityinclinicalprotocols,platformandsamplehandling,andsubtledisease-
relatedsignals,intersectionofpublishedDEGlistswasunabletoestablishconsensusbetweenstudies.Inordertoleverage
the power of multiple transcriptomes reported by several laboratories using different patients and protocols, more
sophisticatedmethodsliketheextensionofGSEApresentedhere,shouldbeusedinordertoovercometheshortcomingsof
overlappingindividualDEGapproach.
Cita
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