7 787

Cited 11 times in

Changes in the biological characteristics of glioma cancer stem cells after serial in vivo subtransplantation.

DC Field Value Language
dc.contributor.author강석구-
dc.contributor.author김동석-
dc.contributor.author김선호-
dc.contributor.author김세훈-
dc.contributor.author김의현-
dc.contributor.author박은경-
dc.contributor.author이지현-
dc.contributor.author장종희-
dc.contributor.author허용민-
dc.date.accessioned2014-12-18T08:21:53Z-
dc.date.available2014-12-18T08:21:53Z-
dc.date.issued2013-
dc.identifier.issn0256-7040-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/86169-
dc.description.abstractPURPOSE: Currently, the interaction between the niche and glioma cancer stem cells (gCSCs) is gaining attention. However, there are few studies concerned with the effects of repeated exposure to a new microenvironment on gCSCs characteristics. In this study, serial in vivo subtransplantation was performed to create a new microenvironment. We evaluated and compared the biological characteristics of gCSCs after serial in vivo subtransplantation. METHODS: We cultured gCSCs from human glioma specimens according to cultured gliomasphere methods. The isolated gCSCs were termed zero-generation gCSCs (G0-gCSCs). By subsequent serial subtransplantation, we obtained first-generation gCSCs (G1-gCSCs) and second-generation gCSCs (G2-gCSCs). We evaluated and compared the biological characteristics of G0-gCSCs, G1-gCSCs, and G2-gCSCs. The in vitro characteristics included the morphology, surface marker profiles, and neural differentiation capacity and the in vivo characteristics was the survival of mice xenografts. Additionally, brain sections were analyzed using PCNA, TUNEL, and CD31 staining. RESULTS: We observed no significant differences in the in vitro characteristics of G0-gCSCs, G1-gCSCs, and G2-gCSCs. However, the survival time of mice glioma xenografts was significantly decreased upon serial subtransplantation. In addition, immunohistochemical analyses showed that the number of TUNEL(+) cells was significantly decreased while the number of CD31(+) cells was significantly increased with serial in vivo subtransplantation. CONCLUSIONS: There were significant in vivo biological changes in gCSCs upon serial in vivo subtransplantation, which were shorter xenograft survival, increased angiogenesis, and decreased apoptosis. This study suggests that the repeated exposure to new microenvironments may affect the biological changes in gCSCs in vivo.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfCHILDS NERVOUS SYSTEM-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAC133 Antigen-
dc.subject.MESHAnimals-
dc.subject.MESHAntigens, CD/metabolism-
dc.subject.MESHBrain Neoplasms/pathology*-
dc.subject.MESHCell Cycle/physiology-
dc.subject.MESHDisease Models, Animal-
dc.subject.MESHFlow Cytometry-
dc.subject.MESHGene Expression Regulation, Neoplastic/physiology*-
dc.subject.MESHGlioblastoma/pathology*-
dc.subject.MESHGlycoproteins/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHIn Situ Nick-End Labeling-
dc.subject.MESHIntermediate Filament Proteins/metabolism-
dc.subject.MESHMembrane Glycoproteins/metabolism-
dc.subject.MESHMice-
dc.subject.MESHMice, Nude-
dc.subject.MESHNeoplasm Transplantation/methods-
dc.subject.MESHNeoplastic Stem Cells/physiology*-
dc.subject.MESHNerve Tissue Proteins/metabolism-
dc.subject.MESHNestin-
dc.subject.MESHPeptides/metabolism-
dc.subject.MESHProliferating Cell Nuclear Antigen/metabolism-
dc.subject.MESHTime Factors-
dc.subject.MESHTransplantation, Heterologous/methods-
dc.subject.MESHTumor Cells, Cultured-
dc.subject.MESHXenograft Model Antitumor Assays/methods-
dc.titleChanges in the biological characteristics of glioma cancer stem cells after serial in vivo subtransplantation.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurosurgery (신경외과학)-
dc.contributor.googleauthorGa-Yeong Shin-
dc.contributor.googleauthorJin-Kyoung Shim-
dc.contributor.googleauthorJi-Hyun Lee-
dc.contributor.googleauthorHye-Jin Shin-
dc.contributor.googleauthorSu-Jae Lee-
dc.contributor.googleauthorYong-Min Huh-
dc.contributor.googleauthorEui-Hyun Kim-
dc.contributor.googleauthorEun-Kyung Park-
dc.contributor.googleauthorSe-Hoon Kim-
dc.contributor.googleauthorJong Hee Chang-
dc.contributor.googleauthorDong-Seok Kim-
dc.contributor.googleauthorYong-Kil Hong-
dc.contributor.googleauthorSun Ho Kim-
dc.contributor.googleauthorSeok-Gu Kang-
dc.contributor.googleauthorFrederick F. Lang-
dc.identifier.doi10.1007/s00381-012-1963-x-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00036-
dc.contributor.localIdA00402-
dc.contributor.localIdA00560-
dc.contributor.localIdA00610-
dc.contributor.localIdA00837-
dc.contributor.localIdA01607-
dc.contributor.localIdA03470-
dc.contributor.localIdA04359-
dc.contributor.localIdA03218-
dc.relation.journalcodeJ00525-
dc.identifier.eissn1433-0350-
dc.identifier.pmid23143001-
dc.identifier.urlhttp://link.springer.com/article/10.1007%2Fs00381-012-1963-x-
dc.subject.keywordGlioma-
dc.subject.keywordGlioma cancer stem cell-
dc.subject.keywordStem cell niche-
dc.subject.keywordSerial subtransplantation-
dc.contributor.alternativeNameKang, Seok Gu-
dc.contributor.alternativeNameKim, Dong Seok-
dc.contributor.alternativeNameKim, Sun Ho-
dc.contributor.alternativeNameKim, Se Hoon-
dc.contributor.alternativeNameKim, Eui Hyun-
dc.contributor.alternativeNamePark, Eun Kyung-
dc.contributor.alternativeNameLee, Ji Hyun-
dc.contributor.alternativeNameChang, Jong Hee-
dc.contributor.alternativeNameHuh, Yong Min-
dc.contributor.affiliatedAuthorKang, Seok Gu-
dc.contributor.affiliatedAuthorKim, Dong Seok-
dc.contributor.affiliatedAuthorKim, Sun Ho-
dc.contributor.affiliatedAuthorKim, Se Hoon-
dc.contributor.affiliatedAuthorKim, Eui Hyun-
dc.contributor.affiliatedAuthorPark, Eun Kyung-
dc.contributor.affiliatedAuthorChang, Jong Hee-
dc.contributor.affiliatedAuthorHuh, Yong Min-
dc.contributor.affiliatedAuthorLee, Ji Hyun-
dc.rights.accessRightsnot free-
dc.citation.volume29-
dc.citation.number1-
dc.citation.startPage55-
dc.citation.endPage64-
dc.identifier.bibliographicCitationCHILDS NERVOUS SYSTEM, Vol.29(1) : 55-64, 2013-
dc.identifier.rimsid28829-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurosurgery (신경외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.