Antagonistic Roles of Notch and P63 in Controlling Mammary Epithelial Cell Fates

dc.contributor.author Yalçın Özuysal, Özden
dc.contributor.author Fiche, M.
dc.contributor.author Guitierrez, M.
dc.contributor.author Wagner, K. U.
dc.contributor.author Raffoul, W.
dc.contributor.author Brisken, C.
dc.coverage.doi 10.1038/cdd.2010.37
dc.date.accessioned 2016-12-21T08:49:36Z
dc.date.available 2016-12-21T08:49:36Z
dc.date.issued 2010
dc.description.abstract The breast epithelium has two major compartments, luminal and basal cells, that are established and maintained by poorly understood mechanisms. The p53 homolog, p63, is required for the formation of mammary buds, but its function in the breast after birth is unknown. We show that in primary human breast epithelial cells, maintenance of basal cell characteristics depends on continued expression of the p63 isoform, ΔNp63, which is expressed in the basal compartment. Forced expression of ΔNp63 in purified luminal cells confers a basal phenotype. Notch signaling downmodulates ΔNp63 expression and mimics ΔNp63 depletion, whereas forced expression of ΔNp63 partially counteracts the effects of Notch. Consistent with Notch activation specifying luminal cell fate in the mammary gland, Notch signaling activity is specifically detected in mice at sites of pubertal ductal morphogenesis where luminal cell fate is determined. Basal cells in which Notch signaling is active show decreased p63 expression. Both constitutive expression of ΔNp63 and ablation of Notch signaling are incompatible with luminal cell fate. Thus, the balance between basal and luminal cell compartments of the breast is regulated by antagonistic functions of ΔNp63 and Notch. © 2010 Macmillan Publishers Limited All rights reserved. en_US
dc.description.sponsorship NCCR Molecular Oncology, Oncosuisse, SNF-3100A0–112090 en_US
dc.identifier.citation Yalçın Özuysal, Ö., Fiche, M., Guitierrez, M., Wagner, K. U., Raffoul, W., and Brisken, C. (2010). Antagonistic roles of Notch and p63 in controlling mammary epithelial cell fates. Cell Death and Differentiation, 17(10), 1600-1612. doi:10.1038/cdd.2010.37 en_US
dc.identifier.doi 10.1038/cdd.2010.37 en_US
dc.identifier.doi 10.1038/cdd.2010.37
dc.identifier.issn 1350-9047
dc.identifier.issn 1476-5403
dc.identifier.scopus 2-s2.0-77956699083
dc.identifier.uri http://doi.org/10.1038/cdd.2010.37
dc.identifier.uri https://hdl.handle.net/11147/2642
dc.language.iso en en_US
dc.publisher Nature Publishing Group en_US
dc.relation.ispartof Cell Death and Differentiation en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Breast epithelium en_US
dc.subject Cell fate en_US
dc.subject Delta notch protein p63 en_US
dc.subject Progenitor en_US
dc.subject Cell differentiation en_US
dc.title Antagonistic Roles of Notch and P63 in Controlling Mammary Epithelial Cell Fates en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Yalçın Özuysal, Özden
gdc.author.yokid 103812
gdc.bip.impulseclass C3
gdc.bip.influenceclass C4
gdc.bip.popularityclass C3
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Molecular Biology and Genetics en_US
gdc.description.endpage 1612 en_US
gdc.description.issue 10 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 1600 en_US
gdc.description.volume 17 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W1965161737
gdc.identifier.pmid 20379195
gdc.identifier.wos WOS:000281745200008
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.impulse 33.0
gdc.oaire.influence 7.253519E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Tumor Suppressor Proteins
gdc.oaire.keywords Delta notch protein p63
gdc.oaire.keywords Apoptosis
gdc.oaire.keywords Epithelial Cells
gdc.oaire.keywords Mice, Transgenic
gdc.oaire.keywords Phosphoproteins
gdc.oaire.keywords Mice
gdc.oaire.keywords Mammary Glands, Animal
gdc.oaire.keywords Cell fate
gdc.oaire.keywords Cell differentiation
gdc.oaire.keywords Trans-Activators
gdc.oaire.keywords Animals
gdc.oaire.keywords Humans
gdc.oaire.keywords Female
gdc.oaire.keywords Receptor, Notch1
gdc.oaire.keywords Mammary Glands, Human
gdc.oaire.keywords Breast epithelium
gdc.oaire.keywords Progenitor
gdc.oaire.keywords Signal Transduction
gdc.oaire.keywords Transcription Factors
gdc.oaire.popularity 3.8653003E-8
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 0303 health sciences
gdc.oaire.sciencefields 03 medical and health sciences
gdc.openalex.collaboration International
gdc.openalex.fwci 5.62551047
gdc.openalex.normalizedpercentile 0.96
gdc.openalex.toppercent TOP 10%
gdc.opencitations.count 137
gdc.plumx.crossrefcites 114
gdc.plumx.mendeley 117
gdc.plumx.pubmedcites 97
gdc.plumx.scopuscites 138
gdc.scopus.citedcount 138
gdc.wos.citedcount 133
relation.isAuthorOfPublication.latestForDiscovery f009792b-87b4-4bc1-88fc-fb55aa7f481c
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4013-8abe-a4dfe192da5e

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