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Dysadherin can enhance tumorigenesis by conferring properties of stem-like cells to hepatocellular carcinoma cells

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dc.contributor.authorPark, Jeong-Ran-
dc.contributor.authorKim, Ran-Ju-
dc.contributor.authorLee, Yoo-Kyung-
dc.contributor.authorKim, Soo-Rim-
dc.contributor.authorRoh, Kyung-Jin-
dc.contributor.authorOh, Seung Hyun-
dc.contributor.authorKong, Gu-
dc.contributor.authorKang, Kyung-Sun-
dc.contributor.authorNam, Jeong-Seok-
dc.date.accessioned2022-07-16T22:19:32Z-
dc.date.available2022-07-16T22:19:32Z-
dc.date.created2021-05-12-
dc.date.issued2011-01-
dc.identifier.issn0168-8278-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/169257-
dc.description.abstractBackground & Aims: Hepatocellular carcinoma (HCC) is associated with a high potential for metastasis and disease recurrence, even after surgical resection. The cancer stem cell (CSC) hypothesis proposes that CSCs are responsible for chemo-resistance, recurrence, and metastasis. Dysadherin is a prognostic indicator of metastasis and poor survival in many different cancer types. In this study, we investigated the possible link between dysadherin and CSC in HCC. Methods: We analyzed the functional implications of dysadherin on cancer sternness by modification of the dysadherin gene in HCC cell lines. Results: The transfection of dysadherin cDNA into the liver cancer cell line PLC/PRF/5 enhanced the properties of CSCs, including anti-apoptosis, their sphere-forming ability, side population phenotype, and tumor initiation ability in vivo. Furthermore, knockdown of dysadherin in the liver cancer cell line SK-Hep1 suppressed its stem cell-like properties. Conclusions: These results show that dysadherin give rise to properties of CSC in HCC. Therefore, these findings suggest that dysadherin may be a potential molecular prognostic marker of HCC and may aid in the development of more effective therapies.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER-
dc.titleDysadherin can enhance tumorigenesis by conferring properties of stem-like cells to hepatocellular carcinoma cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKong, Gu-
dc.identifier.doi10.1016/j.jhep.2010.06.026-
dc.identifier.scopusid2-s2.0-78649636884-
dc.identifier.wosid000286124200020-
dc.identifier.bibliographicCitationJOURNAL OF HEPATOLOGY, v.54, no.1, pp.122 - 131-
dc.relation.isPartOfJOURNAL OF HEPATOLOGY-
dc.citation.titleJOURNAL OF HEPATOLOGY-
dc.citation.volume54-
dc.citation.number1-
dc.citation.startPage122-
dc.citation.endPage131-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusEPITHELIAL-MESENCHYMAL TRANSITION-
dc.subject.keywordPlusCOLORECTAL-CANCER-
dc.subject.keywordPlusSIDE POPULATION-
dc.subject.keywordPlusE-CADHERIN-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusTUMORS-
dc.subject.keywordPlusGLYCOPROTEIN-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusPROMOTES-
dc.subject.keywordAuthorDysadherin-
dc.subject.keywordAuthorHepatocellular carcinoma-
dc.subject.keywordAuthorCancer stem cell-
dc.subject.keywordAuthorSide population-
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