Breast Carcinoma Cells in Primary Tumors and Effusions Have Different Gene Array Profiles英文文献资料.docVIP
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Breast Carcinoma Cells in Primary Tumors and Effusions Have Different Gene Array Profiles英文文献资料
HindawiPublishingCorporation
JournalofOncology
Volume2010,ArticleID969084,14pages
doi:10.1155/2010/969084
ResearchArticle
BreastCarcinomaCellsinPrimaryTumorsandEffusionsHave
DifferentGeneArrayPro?les
SophyaKonstantinovsky, YoavSmith, So?aZilber, HeleneTuftStavnes,
1 2 3 4
Anne-MarieBecker,
4
JahnM.Nesland,4,5ReuvenReich,1,6andBenDavidson 4,5
1
DepartmentofPharmacologyandExperimentalTherapeutics,SchoolofPharmacy,FacultyofMedicine,
TheHebrewUniversityofJerusalem,Jerusalem91120,Israel
2
3
4
5
6
GenomicDataAnalysisUnit,TheHebrewUniversityofJerusalem,Jerusalem91120,Israel
DepartmentofPathology,RabinMedicalCenter,PetachTikva49100,Israel
DivisionofPathology,TheNorwegianRadiumHospital,OsloUniversityHospital,0310Oslo,Norway
FacultyDivisionNorwegianRadiumHospital,TheMedicalFaculty,UniversityofOslo,0316Oslo,Norway
DavidR.BloomCenterforPharmacy,TheHebrewUniversityofJerusalem,Israel
CorrespondenceshouldbeaddressedtoReuvenReich,reich@cc.huji.ac.il
Received22April2009;Accepted2June2009
AcademicEditor:Tian-LiWang
Copyright?2010SophyaKonstantinovskyetal. This is an open access article distributed under the Creative Commons
AttributionLicense,whichpermitsunrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalworkis
properlycited.
Thedetectionofbreastcarcinomacellsine?usionsisassociatedwithrapidlyfataloutcome,butthesecellsarepoorlycharacterized
at the molecular level. This study compared the gene array signatures of breast carcinoma cells in primary carcinomas and
e?usions.Thegeneticsignatureof10primary tumorsand10e?usionswasanalyzedusingtheArray-ReadyOligosetforthe
HumanGenomeplatform.ResultsforselectedgeneswerevalidatedusingPCR,Westernblotting,andimmunohistochemistry.
Array analysis identi?ed 255 signi?cantly downregulated and 96 upregulated genes in the e?usion samples. The majority of
di?erentially expressed genes were part of pathways involved in focal adhesion, extracellular matrix-cell interaction, and the
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