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Proteomic profiling of tumor-initiating cells in HT-29 human colorectal cancer cells

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dc.contributor.authorLee, Han-Na-
dc.contributor.authorPark, Soo-Hyun-
dc.contributor.authorLee, Eun-Kyung-
dc.contributor.authorBernardo, Raymundo-
dc.contributor.authorKim, Chan-Wha-
dc.date.accessioned2021-09-06T14:30:04Z-
dc.date.available2021-09-06T14:30:04Z-
dc.date.created2021-06-15-
dc.date.issued2012-10-12-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/107213-
dc.description.abstractRecent reports have suggested that tumors are organized in heterogeneous populations. Within these populations, a small subpopulation of cells is more capable of initiating malignancy; these are called cancer stem cells. In this study, HT-29 cells were sorted according to the presence or absence of the cancer stem cell marker CD133. We confirmed that CD133+ cells possessed higher clonogenicity compared to CD133- cells. Furthermore, proteomic analysis identified 10 proteins, including actin-related protein 2/3 complex subunit 5-like and profilin 2. In conclusion, our data demonstrated that the expression of specific proteins associated with metastasis and invasion in CD133+ cells contributed to the sternness and tumorigenic properties of these cells. (C) 2012 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectHEPATOCELLULAR-CARCINOMA CELLS-
dc.subjectSTEM-CELLS-
dc.subjectARP2/3 COMPLEX-
dc.subjectIDENTIFICATION-
dc.subjectPROTEIN-
dc.subjectSUBPOPULATION-
dc.subjectEXPRESSION-
dc.subjectPREFOLDIN-
dc.subjectBINDING-
dc.subjectMODEL-
dc.titleProteomic profiling of tumor-initiating cells in HT-29 human colorectal cancer cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chan-Wha-
dc.identifier.doi10.1016/j.bbrc.2012.09.036-
dc.identifier.scopusid2-s2.0-84867646822-
dc.identifier.wosid000310651300030-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.427, no.1, pp.171 - 177-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume427-
dc.citation.number1-
dc.citation.startPage171-
dc.citation.endPage177-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA CELLS-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusARP2/3 COMPLEX-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusSUBPOPULATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPREFOLDIN-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusMODEL-
dc.subject.keywordAuthorCancer stem cell-
dc.subject.keywordAuthorColorectal cancer-
dc.subject.keywordAuthorCD133-
dc.subject.keywordAuthorTwo dimensional gel electrophoresis-
dc.subject.keywordAuthorProteomics-
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