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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 |
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dc.contributor.author | Seok, JY | - |
dc.contributor.author | Na, DC | - |
dc.contributor.author | Woo, HG | - |
dc.contributor.author | Roncalli, M | - |
dc.contributor.author | Kwon, SM | - |
dc.contributor.author | Yoo, JE | - |
dc.contributor.author | Ahn, EY | - |
dc.contributor.author | Kim, GI | - |
dc.contributor.author | Choi, JS | - |
dc.contributor.author | Kim, YB | - |
dc.contributor.author | Park, YN | - |
dc.date.accessioned | 2013-04-22T06:02:16Z | - |
dc.date.available | 2013-04-22T06:02:16Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 0270-9139 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/7796 | - |
dc.description.abstract | Hepatocellular 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.format | application/pdf | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Bile Duct Neoplasms | - |
dc.subject.MESH | Bile Ducts, Intrahepatic | - |
dc.subject.MESH | Carcinoma, Hepatocellular | - |
dc.subject.MESH | Cholangiocarcinoma | - |
dc.subject.MESH | Epithelial-Mesenchymal Transition | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fibrosis | - |
dc.subject.MESH | Gene Expression Profiling | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Liver Neoplasms | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Signal Transduction | - |
dc.subject.MESH | Transforming Growth Factor beta | - |
dc.title | A fibrous stromal component in hepatocellular carcinoma reveals a cholangiocarcinoma-like gene expression trait and epithelial-mesenchymal transition | - |
dc.type | Article | - |
dc.identifier.pmid | 22234953 | - |
dc.contributor.affiliatedAuthor | 우, 현구 | - |
dc.contributor.affiliatedAuthor | 김, 영배 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1002/hep.25570 | - |
dc.citation.title | Hepatology (Baltimore, Md.) | - |
dc.citation.volume | 55 | - |
dc.citation.number | 6 | - |
dc.citation.date | 2012 | - |
dc.citation.startPage | 1776 | - |
dc.citation.endPage | 1786 | - |
dc.identifier.bibliographicCitation | Hepatology (Baltimore, Md.), 55(6). : 1776-1786, 2012 | - |
dc.identifier.eissn | 1527-3350 | - |
dc.relation.journalid | J002709139 | - |
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