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A fibrous stromal component in hepatocellular carcinoma reveals a cholangiocarcinoma-like gene expression trait and epithelial-mesenchymal transition.

DC Field Value Language
dc.contributor.author안의용-
dc.contributor.author유정은-
dc.contributor.author최진섭-
dc.contributor.author김광일-
dc.contributor.author나득채-
dc.contributor.author박영년-
dc.contributor.author석재연-
dc.date.accessioned2014-12-19T16:52:34Z-
dc.date.available2014-12-19T16:52:34Z-
dc.date.issued2012-
dc.identifier.issn0270-9139-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/90360-
dc.description.abstractHepatocellular carcinoma (HCC) and cholangiocarcinoma (CC) are the major primary liver cancers in adults. The phenotypic overlap between HCC and CC has been shown to comprise a continuous liver cancer spectrum. As a proof of this concept, a recent study demonstrated a genomic subtype of HCC that expressed CC-like gene expression traits, such as CC-like HCC, which revealed the common genomic trait of stem-cell-like properties and aggressive clinical outcomes. Scirrhous HCC (S-HCC), a rare variant of HCC, is characterized by abundant fibrous stroma and has been known to express several liver stem/progenitor cell markers. This suggests that S-HCC may harbor common intermediate traits between HCC and CC, including stem-cell traits, which are similar to those of CC-like HCC. However, the molecular and pathological characteristics of S-HCC have not been fully evaluated. By performing gene-expression profiling and immunohistochemical evaluation, we compared the morphological and molecular features of S-HCC with those of CC and HCC. S-HCC expresses both CC-like and stem-cell-like genomic traits. In addition, we observed the expression of core epithelial-mesenchymal transition (EMT)-related genes, which may contribute to the aggressive behavior of S-HCC. Overexpression of transforming growth factor beta (TGF-β) signaling was also found, implying its regulatory role in the pathobiology of S-HCC. Conclusion: We suggest that the fibrous stromal component in HCC may contribute to the acquisition of CC-like gene-expression traits in HCC. The expression of stem-cell-like traits and TGF-β/EMT molecules may play a pivotal role in the aggressive phenotyping of S-HCC. (HEPATOLOGY 2012;55:1776-1786).-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfHEPATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBile Duct Neoplasms/genetics*-
dc.subject.MESHBile Duct Neoplasms/mortality-
dc.subject.MESHBile Duct Neoplasms/pathology-
dc.subject.MESHBile Ducts, Intrahepatic*-
dc.subject.MESHCarcinoma, Hepatocellular/mortality-
dc.subject.MESHCarcinoma, Hepatocellular/pathology*-
dc.subject.MESHCholangiocarcinoma/genetics*-
dc.subject.MESHCholangiocarcinoma/mortality-
dc.subject.MESHCholangiocarcinoma/pathology-
dc.subject.MESHEpithelial-Mesenchymal Transition*-
dc.subject.MESHFemale-
dc.subject.MESHFibrosis-
dc.subject.MESHGene Expression Profiling-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms/mortality-
dc.subject.MESHLiver Neoplasms/pathology*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHSignal Transduction-
dc.subject.MESHTransforming Growth Factor beta/physiology-
dc.titleA fibrous stromal component in hepatocellular carcinoma reveals a cholangiocarcinoma-like gene expression trait and epithelial-mesenchymal transition.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.googleauthorJae Yeon Seok-
dc.contributor.googleauthorDeuk Chae Na-
dc.contributor.googleauthorHyun Goo Woo-
dc.contributor.googleauthorMassimo Roncalli-
dc.contributor.googleauthorSo Mee Kwon-
dc.contributor.googleauthorJeong Eun Yoo-
dc.contributor.googleauthorEi Yong Ahn-
dc.contributor.googleauthorGwang Il Kim-
dc.contributor.googleauthorJin-Sub Choi-
dc.contributor.googleauthorYoung Bae Kim-
dc.contributor.googleauthorYoung Nyun Park-
dc.identifier.doi22234953-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02504-
dc.contributor.localIdA02253-
dc.contributor.localIdA04199-
dc.contributor.localIdA00316-
dc.contributor.localIdA01231-
dc.contributor.localIdA01563-
dc.contributor.localIdA01928-
dc.relation.journalcodeJ00985-
dc.identifier.eissn1527-3350-
dc.identifier.pmid22234953-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1002/hep.25570/abstract-
dc.subject.keywordAdult-
dc.subject.keywordAged-
dc.subject.keywordAged, 80 and over-
dc.subject.keywordBile Duct Neoplasms/genetics*-
dc.subject.keywordBile Duct Neoplasms/mortality-
dc.subject.keywordBile Duct Neoplasms/pathology-
dc.subject.keywordBile Ducts, Intrahepatic*-
dc.subject.keywordCarcinoma, Hepatocellular/mortality-
dc.subject.keywordCarcinoma, Hepatocellular/pathology*-
dc.subject.keywordCholangiocarcinoma/genetics*-
dc.subject.keywordCholangiocarcinoma/mortality-
dc.subject.keywordCholangiocarcinoma/pathology-
dc.subject.keywordEpithelial-Mesenchymal Transition*-
dc.subject.keywordFemale-
dc.subject.keywordFibrosis-
dc.subject.keywordGene Expression Profiling-
dc.subject.keywordHumans-
dc.subject.keywordLiver Neoplasms/mortality-
dc.subject.keywordLiver Neoplasms/pathology*-
dc.subject.keywordMale-
dc.subject.keywordMiddle Aged-
dc.subject.keywordSignal Transduction-
dc.subject.keywordTransforming Growth Factor beta/physiology-
dc.contributor.alternativeNameAhn, Ei Yong-
dc.contributor.alternativeNameYoo, Jeong Eun-
dc.contributor.alternativeNameChoi, Jin Sub-
dc.contributor.alternativeNameKim, Gwang Il-
dc.contributor.alternativeNameNa, Deuk Chae-
dc.contributor.alternativeNamePark, Young Nyun-
dc.contributor.alternativeNameSeok, Jae Yeon-
dc.contributor.affiliatedAuthorYoo, Jeong Eun-
dc.contributor.affiliatedAuthorAhn, Ei Yong-
dc.contributor.affiliatedAuthorChoi, Jin Sub-
dc.contributor.affiliatedAuthorKim, Gwang Il-
dc.contributor.affiliatedAuthorNa, Deuk Chae-
dc.contributor.affiliatedAuthorPark, Young Nyun-
dc.contributor.affiliatedAuthorSeok, Jae Yeon-
dc.citation.volume55-
dc.citation.number6-
dc.citation.startPage1776-
dc.citation.endPage1786-
dc.identifier.bibliographicCitationHEPATOLOGY, Vol.55(6) : 1776-1786, 2012-
dc.identifier.rimsid34164-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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