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BMP-2 induces motility and invasiveness by promoting colon cancer stemness through STAT3 activation

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dc.contributor.authorKim, Bo Ram-
dc.contributor.authorOh, Sang Cheul-
dc.contributor.authorLee, Dae-Hee-
dc.contributor.authorKim, Jung Lim-
dc.contributor.authorLee, Suk Young-
dc.contributor.authorKang, Myoung Hee-
dc.contributor.authorLee, Sun Il-
dc.contributor.authorKang, Sanghee-
dc.contributor.authorJoung, Sung Yup-
dc.contributor.authorMin, Byung Wook-
dc.date.available2020-11-02T14:41:16Z-
dc.date.issued2015-12-
dc.identifier.issn1010-4283-
dc.identifier.issn1423-0380-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/7255-
dc.description.abstractBone morphogenetic proteins (BMPs) have been involved in metastatic progression and tumorigenesis of many cancer types. However, it remains unclear how BMP-2 contributes to the initiation and development of these cancers. Here, we investigated the role of BMP-2 in colon cancer stem cell (CSC) development from colon cancer cells. We also determined the effects of BMP-2 on CSC development and epithelial-mesenchymal transition (EMT) in human colon cancer cell lines HCT-116 and SW620. We found that BMP-2 enhanced sphere formation of colon cancer cells without serum. Also, BMP-2-induced spheres displayed up-regulation of stemness markers (CD133+ and EpCAM+) and increased drug resistance, hallmarks of CSCs. Importantly, expression of EMT activators p-Smad1/5 and Snail and N-cadherin was increased in the spheres' cells, indicating that BMP-2 signaling might result in CSC self-renewal and EMT. Furthermore, siRNA-mediated knockdown of signal transducer and activator of transcription 3 (STAT3) in HCT-116 cells reversed BMP-2-induced EMT and stem cell formation. Taken together, our results suggest that the BMP-2 induced STAT3-mediated induction of colon cancer cell metastasis requires an EMT and/or changes in CSC markers.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherSAGE PUBLICATIONS LTD-
dc.titleBMP-2 induces motility and invasiveness by promoting colon cancer stemness through STAT3 activation-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1007/s13277-015-3681-y-
dc.identifier.scopusid2-s2.0-84952873854-
dc.identifier.wosid000367329300042-
dc.identifier.bibliographicCitationTUMOR BIOLOGY, v.36, no.12, pp 9475 - 9486-
dc.citation.titleTUMOR BIOLOGY-
dc.citation.volume36-
dc.citation.number12-
dc.citation.startPage9475-
dc.citation.endPage9486-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusBONE MORPHOGENETIC PROTEIN-2-
dc.subject.keywordPlusEPITHELIAL-MESENCHYMAL TRANSITIONS-
dc.subject.keywordPlusPHOSPHATIDYLINOSITOL 3-KINASE-
dc.subject.keywordPlusCHONDROSARCOMA CELLS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusAKT-
dc.subject.keywordPlusPI3K/AKT-
dc.subject.keywordPlusKINASE-
dc.subject.keywordPlusMAPK-
dc.subject.keywordAuthorColon cancer-
dc.subject.keywordAuthorBone morphogenetic proteins-
dc.subject.keywordAuthorCancer stem cells-
dc.subject.keywordAuthorEpithelial-mesenchymal transition-
dc.subject.keywordAuthorSignal transducer and activator of transcription 3-
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