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Hepatocellular Carcinomas Expressing ‘Stemness’-Related Markers:Clinicopathological Characteristics

DC Field Value Language
dc.contributor.author박영년-
dc.date.accessioned2015-12-28T10:58:11Z-
dc.date.available2015-12-28T10:58:11Z-
dc.date.issued2014-
dc.identifier.issn0257-2753-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/138413-
dc.description.abstractHepatocellular carcinoma (HCC) is heterogeneous in histopathology, pathogenesis and biological behavior. There is accumulating evidence that the expression of 'stemness'-related markers such as K19, EpCAM and CD133 in HCC is associated with an aggressive biological behavior and poor clinical outcome compared to conventional HCCs that do not express stemness-related markers. Compared to conventional HCCs, these tumors more frequently demonstrate infiltrative growth patterns, vascular invasion and more intratumoral fibrous stroma, and there is a spectrum of morphological and immunophenotypic features between HCCs with stemness-related marker expression, scirrhous HCCs and combined hepatocellular-cholangiocarcinoma with stem cell features. Clinically, HCCs with stemness-related marker expression are associated with increased serum α-fetoprotein levels and a poor prognosis, and are also beginning to be noticed radiologically. These tumors have also been recognized as a specific subtype in recent molecular classifications, and increasing interest in the molecular pathogenesis of HCCs with stemness-related marker expression will shed light on the development of targeted therapy for these tumors. Therefore, it is important that pathologists identify HCCs expressing stemness-related markers such as K19 during routine pathological evaluation of surgically resected or biopsied HCC tissue, as it will help to identify a high-risk subgroup of HCCs characterized by increased chemoresistance, earlier recurrence after surgical and/or locoregional treatment, increased invasiveness/metastasis and poor overall survival. We will discuss the clinicopathological characteristics of a HCC subtype expressing stemness-related markers and its future perspectives.-
dc.description.statementOfResponsibilityopen-
dc.format.extent778~785-
dc.relation.isPartOfDIGESTIVE DISEASES-
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.MESHAntigens, CD/analysis-
dc.subject.MESHAntigens, Neoplasm/analysis-
dc.subject.MESHBiomarkers, Tumor/analysis*-
dc.subject.MESHBiopsy, Needle-
dc.subject.MESHCarcinoma, Hepatocellular/chemistry*-
dc.subject.MESHCarcinoma, Hepatocellular/pathology*-
dc.subject.MESHCell Adhesion Molecules/analysis-
dc.subject.MESHEpithelial Cell Adhesion Molecule-
dc.subject.MESHFemale-
dc.subject.MESHGlycoproteins/analysis-
dc.subject.MESHHumans-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHLiver Neoplasms/chemistry*-
dc.subject.MESHLiver Neoplasms/pathology*-
dc.subject.MESHMale-
dc.subject.MESHNeoplasm Invasiveness/pathology-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHNeoplastic Stem Cells/pathology*-
dc.subject.MESHPeptides/analysis-
dc.subject.MESHPrognosis-
dc.subject.MESHSensitivity and Specificity-
dc.subject.MESHalpha-Fetoproteins/analysis-
dc.titleHepatocellular Carcinomas Expressing ‘Stemness’-Related Markers:Clinicopathological Characteristics-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학)-
dc.contributor.googleauthorHaeryoung Kim-
dc.contributor.googleauthorYoung Nyun Park-
dc.identifier.doi10.1159/000368021-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01563-
dc.relation.journalcodeJ00736-
dc.identifier.eissn1421-9875-
dc.identifier.pmid25376296-
dc.identifier.urlhttp://www.karger.com/Article/FullText/368021-
dc.subject.keywordHepatocellular carcinoma-
dc.subject.keywordK19-
dc.subject.keywordPrognosis-
dc.subject.keywordStemness-
dc.contributor.alternativeNamePark, Young Nyun-
dc.contributor.affiliatedAuthorPark, Young Nyun-
dc.rights.accessRightsfree-
dc.citation.volume32-
dc.citation.number6-
dc.citation.startPage778-
dc.citation.endPage785-
dc.identifier.bibliographicCitationDIGESTIVE DISEASES, Vol.32(6) : 778-785, 2014-
dc.identifier.rimsid49161-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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