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Cited 152 time in webofscience Cited 160 time in scopus
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dc.contributor.authorShin, K-
dc.contributor.authorLim, A-
dc.contributor.authorZhao, C-
dc.contributor.authorSahoo, D-
dc.contributor.authorPan, Y-
dc.contributor.authorSpiekerkoetter, E-
dc.contributor.authorLiao, JC-
dc.contributor.authorBeachy, PA-
dc.date.accessioned2017-07-19T12:32:36Z-
dc.date.available2017-07-19T12:32:36Z-
dc.date.created2016-04-05-
dc.date.issued2014-10-13-
dc.identifier.issn1535-6108-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/36006-
dc.description.abstractHedgehog (Hh) pathway inhibitors are clinically effective in treatment of basal cell carcinoma and medulloblastoma, but fail therapeutically or accelerate progression in treatment of endodermally derived colon and pancreatic cancers. In bladder, another organ of endodermal origin, we find that despite its initial presence in the cancer cell of origin Sonic hedgehog (Shh) expression is invariably lost during progression to invasive urothelial carcinoma. Genetic blockade of stromal response to Shh furthermore dramatically accelerates progression and decreases survival time. This cancer-restraining effect of Hh pathway activity is associated with stromal expression of BMP signals, which stimulate urothelial differentiation. Progression is dramatically reduced by pharmacological activation of BMP pathway activity with low-dose FK506, suggesting an approach to management of human bladder cancer.-
dc.languageEnglish-
dc.publisherCell Press-
dc.relation.isPartOfCANCER CELL-
dc.titleHedgehog signaling restrains bladder cancer progression by eliciting stromal production of urothelial differentiation factors-
dc.typeArticle-
dc.identifier.doi10.1016/j.ccell.2014.09.001-
dc.type.rimsART-
dc.identifier.bibliographicCitationCANCER CELL, v.26, no.4, pp.521 - 533-
dc.identifier.wosid000343343800012-
dc.date.tcdate2019-03-01-
dc.citation.endPage533-
dc.citation.number4-
dc.citation.startPage521-
dc.citation.titleCANCER CELL-
dc.citation.volume26-
dc.contributor.affiliatedAuthorShin, K-
dc.identifier.scopusid2-s2.0-84907996793-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc49-
dc.type.docTypeArticle-
dc.subject.keywordPlusSONIC HEDGEHOG-
dc.subject.keywordPlusHUMAN HOMOLOG-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusBASAL-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusMEDULLOBLASTOMA-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusPATHOGENESIS-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaCell Biology-

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신근유SHIN, KUNYOO
Dept of Life Sciences
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