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dc.contributor.author서용준-
dc.date.accessioned2017-03-06T07:06:33Z-
dc.date.available2017-03-06T07:06:33Z-
dc.date.issued2015-06-
dc.identifier.citationCANCER SCIENCE, v. 106, NO 6, Page. 718-725en_US
dc.identifier.issn1347-9032-
dc.identifier.issn1349-700-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1111/cas.12668/abstract-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/25869-
dc.description.abstractMetastasis of breast cancer is promoted by epithelial-mesenchymal transition (EMT). Emerging evidence suggests that STAT3 is a critical signaling node in EMT and is constitutively activated in many carcinomas, including breast cancer. However, its signaling mechanisms underlying persistent activation of STAT3 associated with EMT remain obscure. Here, we report that PIM2 promotes activation of STAT3 through induction of cytokines. Activation of STAT3 caused an increase in PIM2 expression, implicating a positive feedback loop between PIM2 and STAT3. In agreement, targeting of either PIM2, STAT3 or PIM2-dependent cytokines suppressed EMT-associated migratory and invasive properties through inhibition of ZEB1. Taken together, our findings identify the signaling mechanisms underlying the persistent activation of STAT3 and the oncogenic role of PIM2 in EMT in breast cancer.en_US
dc.description.sponsorshipThis work was supported by Basic Science Research Program (NRF-2012R1A1A2044683) and National Nuclear Technology Program (NRF-2014M2A2A7045072) through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning.en_US
dc.language.isoenen_US
dc.publisherWILEY-BLACKWELLen_US
dc.subjectCytokinesen_US
dc.subjectepithelial-mesenchymal transitionen_US
dc.subjectPIM2en_US
dc.subjectpositive feedback loopen_US
dc.subjectSTAT3en_US
dc.titlePersistent activation of STAT3 by PIM2-driven positive feedback loop for epithelial-mesenchymal transition in breast canceren_US
dc.typeArticleen_US
dc.relation.no6-
dc.relation.volume106-
dc.identifier.doi10.1111/cas.12668-
dc.relation.page718-725-
dc.relation.journalCANCER SCIENCE-
dc.contributor.googleauthorUddin, Nizam-
dc.contributor.googleauthorKim, Rae-Kwon-
dc.contributor.googleauthorYoo, Ki-Chun-
dc.contributor.googleauthorKim, Young-Heon-
dc.contributor.googleauthorCui, Yan-Hong-
dc.contributor.googleauthorKim, In-Gyu-
dc.contributor.googleauthorSuh, Yongjoon-
dc.contributor.googleauthorLee, Su-Jae-
dc.relation.code2015001495-
dc.sector.campusS-
dc.sector.daehakRESEARCH INSTITUTE[S]-
dc.sector.departmentTHE RESEARCH INSTITUTE FOR NATURAL SCIENCES-
dc.identifier.pidsuh-


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