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dc.contributor.authorZengin, T.
dc.contributor.authorEkinci, B.
dc.contributor.authorKucukkose, C.
dc.contributor.authorYalcin-Ozuysal, O.
dc.date.accessioned2020-11-20T16:48:20Z
dc.date.available2020-11-20T16:48:20Z
dc.date.issued2015
dc.identifier.issn1932-6203
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0132757
dc.identifier.urihttps://hdl.handle.net/20.500.12809/6007
dc.descriptionPubMed ID: 26161746en_US
dc.description.abstractIRF6, a member of Interferon Regulatory Factors (IRF) family, is involved in orofacial and epidermal development. In breast cancer cell lines ectopic expression of IRF6 reduces cell numbers suggesting a role as negative regulator of cell cycle. IRF6 is a direct target of canonical Notch signaling in keratinocyte differentiation. Notch is involved in luminal cell fate determination and stem cell regulation in the normal breast and is implicated as an oncogene in breast cancer. Notch activation is sufficient to induce proliferation and transformation in non-tumorigenic breast epithelial cell line, MCF10A. ?Np63, which is downregulated by Notch activation in the breast, regulates IRF6 expression in keratinocytes. In this report, we investigate Notch-IRF6 and ?Np63-IRF6 interactions in MCF10A and MDA MB 231 cells. We observed that in these cells, IRF6 expression is partially regulated by canonical Notch signaling and ?Np63 downregulation. Furthermore, we demonstrate that IRF6 abrogation impairs Notch-induced proliferation and transformation in MCF10A cells. Thus, we confirm the previous findings by showing a tissue independent regulation of IRF6 by Notch signaling, and extend them by proposing a context dependent role for IRF6, which acts as a positive regulator of proliferation and transformation in MCF10A cells downstream of Notch signaling. Copyright: © 2015 Zengin et al.en_US
dc.item-language.isoengen_US
dc.publisherPublic Library of Scienceen_US
dc.item-rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleIRF6 is involved in the regulation of cell proliferation and transformation in MCF10A cells downstream of notch signalingen_US
dc.item-typearticleen_US
dc.contributor.departmenten_US
dc.contributor.departmentTempZengin, T., Department of Molecular Biology and Genetic, Izmir Institute of Technology, Izmir, Turkey, Department of Molecular Biology and Genetics, Muğla Sitki Koçman University, Muğla, Turkey; Ekinci, B., Department of Molecular Biology and Genetic, Izmir Institute of Technology, Izmir, Turkey; Kucukkose, C., Department of Molecular Biology and Genetic, Izmir Institute of Technology, Izmir, Turkey; Yalcin-Ozuysal, O., Department of Molecular Biology and Genetic, Izmir Institute of Technology, Izmir, Turkeyen_US
dc.identifier.doi10.1371/journal.pone.0132757
dc.identifier.volume10en_US
dc.identifier.issue7en_US
dc.relation.journalPLoS ONEen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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