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dc.contributor.authorFarnie, Gillian
dc.contributor.authorClarke, Robert B
dc.date.accessioned2009-07-07T11:59:47Z
dc.date.available2009-07-07T11:59:47Z
dc.date.issued2006
dc.identifier.citationBreast stem cells and cancer. 2006 (5):141-53 Ernst Schering Found Symp Procen
dc.identifier.pmid17939300
dc.identifier.doi10.1007/2789_2007_049
dc.identifier.urihttp://hdl.handle.net/10541/72747
dc.description.abstractRecent results have increased our understanding of normal stem cells and the signalling pathways which regulate them during the development of the mammary gland. Tumours in many tissues are now thought to develop from dysregulated stem cells and depend on activated stem cell self-renewal pathways such as Notch for their tumourigenic capacity. These cancer stem cells are recognised by specific cell surface proteins that they express and their capacity to grow tumours in vivo or spheres in vitro. We have described human breast DCIS mammospheres grown from cancer stem cells and demonstrated their dependence on the EGF and Notch receptor pathways. Stem cell self-renewal pathways such as these may represent novel therapeutic targets to prevent recurrence of pre-invasive and invasive breast cancer.
dc.language.isoenen
dc.subjectBreast Canceren
dc.subject.meshBreast
dc.subject.meshBreast Neoplasms
dc.subject.meshEpidermal Growth Factor
dc.subject.meshHumans
dc.subject.meshReceptors, Notch
dc.subject.meshSignal Transduction
dc.subject.meshStem Cells
dc.titleBreast stem cells and cancer.en
dc.typeArticleen
dc.contributor.departmentBreast Biology Group, School of Cancer and Imaging Sciences, Faculty of Medicine and Human Sciences, University of Manchester, Paterson Institute for Cancer Research, Wilmslow Road, M20 4BX Manchester, UK.en
dc.identifier.journalErnst Schering Foundation Symposium Proceedingsen
html.description.abstractRecent results have increased our understanding of normal stem cells and the signalling pathways which regulate them during the development of the mammary gland. Tumours in many tissues are now thought to develop from dysregulated stem cells and depend on activated stem cell self-renewal pathways such as Notch for their tumourigenic capacity. These cancer stem cells are recognised by specific cell surface proteins that they express and their capacity to grow tumours in vivo or spheres in vitro. We have described human breast DCIS mammospheres grown from cancer stem cells and demonstrated their dependence on the EGF and Notch receptor pathways. Stem cell self-renewal pathways such as these may represent novel therapeutic targets to prevent recurrence of pre-invasive and invasive breast cancer.


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