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dc.contributor.authorYun, Eun-Jin-
dc.contributor.author김동휘-
dc.contributor.authorHsieh, Jer-Tsong-
dc.contributor.author백승태-
dc.date.accessioned2022-09-29T04:20:06Z-
dc.date.available2022-09-29T04:20:06Z-
dc.date.created2022-07-13-
dc.date.issued2022-12-
dc.identifier.issn2058-7716-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/113849-
dc.description.abstract<jats:title>Abstract</jats:title><jats:p>Glioblastoma multiforme (GBM) is the most malignant brain tumor and is refractory to conventional therapies. Although previous studies have proposed that the interaction between gene mutations and the external environment leads to the occurrence of GBM, the pathogenesis of GBM is still unclear and much remains to be studied. Herein, we show an association between human glycoprotein stanniocalcin-2 (STC2) and aggressive GBM progression, and demonstrate the underlying mechanism. Elevated STC2 expression and secretion greatly increase GBM cell growth and invasive phenotypes. Mechanistically, both, conditioned media (CM) containing STC2 and recombinant STC2, can induce the transformation of GBM cells into more malignant phenotypes by upregulating the expression of the epithelial-mesenchymal transition transcription factor, snail family transcription repressor 2 (SNAI2) as well as matrix metalloproteinases (MMPs). Moreover, we further demonstrate that the oncogenic function of STC2 in GBM is mediated through the MAPK signaling pathway. Collectively, these results identify the mechanism of STC2 targeting SNAI2 and MMPs through the MAPK pathway in GBM, and provide insights into a potential therapeutic strategy for GBM.</jats:p>-
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.relation.isPartOfCell Death Discovery-
dc.titleStanniocalcin 2 drives malignant transformation of human glioblastoma cells by targeting SNAI2 and Matrix Metalloproteinases-
dc.typeArticle-
dc.identifier.doi10.1038/s41420-022-01090-6-
dc.type.rimsART-
dc.identifier.bibliographicCitationCell Death Discovery, v.8, no.1-
dc.identifier.wosid000821010400001-
dc.citation.number1-
dc.citation.titleCell Death Discovery-
dc.citation.volume8-
dc.contributor.affiliatedAuthorYun, Eun-Jin-
dc.contributor.affiliatedAuthor김동휘-
dc.contributor.affiliatedAuthor백승태-
dc.identifier.scopusid2-s2.0-85133474119-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.type.docTypeArticle-
dc.subject.keywordPlusEPITHELIAL-MESENCHYMAL TRANSITION-
dc.subject.keywordPlusMOLECULAR-CLONING-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusCALCIUM-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusSTC2-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusTEMOZOLOMIDE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCARCINOMA-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-

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백승태BAEK, SEUNG TAE
Dept of Life Sciences
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