Multiple Lineages of Human Breast Cancer StemProgenitor Cells Identified by Profiling with Stem Cell Markers 英文参考文献.docVIP
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Multiple Lineages of Human Breast Cancer StemProgenitor Cells Identified by Profiling with Stem Cell Markers 英文参考文献
MultipleLineagesofHumanBreastCancerStem/
ProgenitorCellsIdentifiedbyProfilingwithStemCell
Markers
WendyW.Hwang-Verslues1,Wen-HungKuo2,Po-HaoChang1,Chi-ChunPan1,Hsing-HuiWang1 ,Sheng-
TaTsai1,Yung-MingJeng3,Jin-YuShew1,JohnT.Kung4,Chung-HsuanChen1,EvaY.-H.P.Lee1,5,6* ,King-
JenChang2*,Wen-HwaLee1,6*
1GenomicsResearchCenter,AcademiaSinica,Taipei,Taiwan,2DepartmentofSurgery,NationalTaiwanUniversityHospital,Taipei,Taiwan,3DepartmentofPathology,National
TaiwanUniversityHospital,Taipei,Taiwan,4InstituteofMolecularBiology,AcademiaSinica,Taipei,Taiwan,5DepartmentofDevelopmentandCellBiology,Universityof
CaliforniaIrvine,Irvine,California,UnitedStatesofAmerica,6DepartmentofBiologicalChemistry,UniversityofCaliforniaIrvine,Irvine,California,UnitedStatesofAmerica
Abstract
Heterogeneityofcancerstem/progenitorcellsthatgiverisetodifferentformsofcancerhasbeenwelldemonstratedfor
leukemia. However, this fundamental concept has yet to be established for solid tumors including breast cancer. In this
communication,weanalyzedsolidtumorcancerstemcellmarkersinhumanbreastcancercelllinesandprimaryspecimens
using flow cytometry. The stem/progenitor cell properties of different marker expressing-cell populations were further
assessedbyinvitrosoftagarcolonyformationassayandtheabilitytoformtumorsinNOD/SCIDmice.Wefoundthatthe
expressionofstemcellmarkersvariedgreatlyamongbreastcancercelllines.InMDA-MB-231cells,PROCRandESA,instead
+
ofthewidelyusedbreastcancerstemcellmarkersCD44 /CD24-/lowandALDH,couldbeusedtohighlyenrichcancerstem/
progenitorcellpopulationswhichexhibitedtheabilitytoselfrenewanddivideasymmetrically.Furthermore,thePROCR+/
+
ESA
cells expressed epithelial-mesenchymal transition markers. PROCR could also be used to enrich cells with colony
formingabilityfromMB-361cells.Moreover,consistentwiththemarkerprofilingusingcelllines,theexpressionofstemcell
markersdifferedgreatlyamongprimarytumors.Therewasanassociationbetweenmetastasisstatusandahighprevalence
ofcertainmarkersincludingCD44
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