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Cited 14 time in webofscience Cited 16 time in scopus
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Tumor-associated mesenchymal stem-like cells provide extracellular signaling cue for invasiveness of glioblastoma cells

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dc.contributor.authorLim, Eun-Jung-
dc.contributor.authorSuh, Yongjoon-
dc.contributor.authorYoo, Ki-Chun-
dc.contributor.authorLee, Ji-Hyun-
dc.contributor.authorKim, In-Gyu-
dc.contributor.authorKim, Min-Jung-
dc.contributor.authorChang, Jong Hee-
dc.contributor.authorKang, Seok-Gu-
dc.contributor.authorLee, Su-Jae-
dc.date.accessioned2021-08-02T15:52:04Z-
dc.date.available2021-08-02T15:52:04Z-
dc.date.issued2017-01-
dc.identifier.issn1949-2553-
dc.identifier.issn1949-2553-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/21248-
dc.description.abstractHyaluronic acid (HA) is abundant in tumor microenvironment and closely associated with invasiveness of glioblastoma (GM) cells. However, the cellular mechanism underlying HA-rich microenvironment in GBM remains unexplored. Here, we show that tumor-associated mesenchymal stem-like cells (tMSLCs) contribute to abundance of hyaluronic acid (HA) in tumor microenvironment through HA synthase-2 (HAS2) induction, and thereby enhances invasiveness of GBM cells. In an autocrine manner, C5a secreted by tMSLCs activated ERK MAPK for HAS2 induction in tMSLCs. Importantly, HA acted as a signaling ligand of its cognate receptor RHAMM for intracellular signaling activation underlying invasiveness of GBM cells. Taken together, our study suggests that tMSLCs contribute to HA-rich proinvasive ECM microenvironment in GBM.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherImpact Journals-
dc.titleTumor-associated mesenchymal stem-like cells provide extracellular signaling cue for invasiveness of glioblastoma cells-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.18632/oncotarget.13638-
dc.identifier.scopusid2-s2.0-85009753150-
dc.identifier.wosid000391503300112-
dc.identifier.bibliographicCitationOncotarget, v.8, no.1, pp 1438 - 1448-
dc.citation.titleOncotarget-
dc.citation.volume8-
dc.citation.number1-
dc.citation.startPage1438-
dc.citation.endPage1448-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusANAPHYLATOXIN C5A-
dc.subject.keywordPlusBRAIN-TUMOR-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusHYALURONAN-
dc.subject.keywordPlusMATRIX-
dc.subject.keywordPlusMODULATION-
dc.subject.keywordPlusGLIOMAS-
dc.subject.keywordPlusTARGET-
dc.subject.keywordPlusC3A-
dc.subject.keywordAuthorextracellular matrix remodeling-
dc.subject.keywordAuthormesenchymal stem-like cells-
dc.subject.keywordAuthorhyaluronic acid-
dc.subject.keywordAuthorhyaluronic acid synthase-2-
dc.subject.keywordAuthorC5a-
dc.identifier.urlhttps://www.oncotarget.com/article/13638/text/-
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