Expression of β-catenin in hepatocellular carcinoma

AIM: The β-catenin has been recognized as a critical member of the Wnt signaling pathway and plays an important role in the generation/differentiation of many tissues. Inappropriate activation of this pathway has been implicated in carcinogenesis. The mechanism underlying the development as well as...

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Veröffentlicht in:World journal of gastroenterology : WJG 2005-04, Vol.11 (16), p.2398-2401
Hauptverfasser: Tien, Liem Thanh, Ito, Masahiro, Nakao, Mikiko, Niino, Daisuke, Serik, Meirmanov, Nakashima, Masahiro, Wen, Chun-Yang, Yatsuhashi, Hiroshi, Ishibashi, Hiromi
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container_issue 16
container_start_page 2398
container_title World journal of gastroenterology : WJG
container_volume 11
creator Tien, Liem Thanh
Ito, Masahiro
Nakao, Mikiko
Niino, Daisuke
Serik, Meirmanov
Nakashima, Masahiro
Wen, Chun-Yang
Yatsuhashi, Hiroshi
Ishibashi, Hiromi
description AIM: The β-catenin has been recognized as a critical member of the Wnt signaling pathway and plays an important role in the generation/differentiation of many tissues. Inappropriate activation of this pathway has been implicated in carcinogenesis. The mechanism underlying the development as well as its prognosis of hepatocellular carcinoma (HCC) has remained unclear. The purpose of this study is to analyze the expression of β-catenin in HCC in relation to histological grades and viral hepatitis backgrounds. METHODS: Thirty-two sections were selected at random from autopsy and surgical cases of HCC. Immuohistologically, the location and positivity of β-catenin expression in HCC was examined. RESULTS: Normal hepatocytes did not express β-catenin. In 78% of HCC β-catenin was expressed at the membrane of the cells, with or without cytoplasmic and/or nuclear expression. The tumor cells with well- and moderately-differentiated grades expressed frequently at the membrane and cytoplasm compared with poorly-differentiated type. Nuclear expression of β-catenin was prone to occur in the tumor cells of poorly-differentiated grade. There were 15% of hepatitis C virus (HCV) backgrounds with nuclear expression. In contrast, there was 38% with nuclear expression in hepatitis B virus (HBV) backgrounds. In nonBnonC hepatitis, no case expressed nuclear β-catenin. CONCLUSION: The β-catenin expression in HCC cells was heterogenous among types of hepatitis viral infection. Wnt signaling pathway might be deeply involved in less-differentiated HCC and HBV background.
doi_str_mv 10.3748/wjg.v11.i16.2398
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Inappropriate activation of this pathway has been implicated in carcinogenesis. The mechanism underlying the development as well as its prognosis of hepatocellular carcinoma (HCC) has remained unclear. The purpose of this study is to analyze the expression of β-catenin in HCC in relation to histological grades and viral hepatitis backgrounds. METHODS: Thirty-two sections were selected at random from autopsy and surgical cases of HCC. Immuohistologically, the location and positivity of β-catenin expression in HCC was examined. RESULTS: Normal hepatocytes did not express β-catenin. In 78% of HCC β-catenin was expressed at the membrane of the cells, with or without cytoplasmic and/or nuclear expression. The tumor cells with well- and moderately-differentiated grades expressed frequently at the membrane and cytoplasm compared with poorly-differentiated type. Nuclear expression of β-catenin was prone to occur in the tumor cells of poorly-differentiated grade. There were 15% of hepatitis C virus (HCV) backgrounds with nuclear expression. In contrast, there was 38% with nuclear expression in hepatitis B virus (HBV) backgrounds. In nonBnonC hepatitis, no case expressed nuclear β-catenin. CONCLUSION: The β-catenin expression in HCC cells was heterogenous among types of hepatitis viral infection. Wnt signaling pathway might be deeply involved in less-differentiated HCC and HBV background.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v11.i16.2398</identifier><identifier>PMID: 15832407</identifier><language>eng</language><publisher>United States: Department of Pathology, National Nagasaki Medical Center, 2-1001-1 Kubara,Omura, Nagasaki 856-8562, Japan%Department of Molecular Pathology, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Science, 1-12-4 Sakamoto,Nagasaki 852-8523, Japan%Tissue and Histopathology Section Division of Scientific Data Registry, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Science, 1-12-4 Sakamoto,Nagasaki 852-8523, Japan%Department of Molecular Pathology, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Science, 1-12-4 Sakamoto,Nagasaki 852-8523, Japan</publisher><subject>Adult ; Aged ; Aged, 80 and over ; beta Catenin ; Carcinoma, Hepatocellular - metabolism ; Carcinoma, Hepatocellular - pathology ; Cytoskeletal Proteins - metabolism ; Female ; Hepatitis, Viral, Human - metabolism ; Hepatitis, Viral, Human - pathology ; Humans ; Immunohistochemistry ; Intercellular Signaling Peptides and Proteins - metabolism ; Liver Cancer ; Liver Neoplasms - metabolism ; Liver Neoplasms - pathology ; Male ; Middle Aged ; Retrospective Studies ; Signal Transduction - physiology ; Trans-Activators - metabolism ; Wnt Proteins ; β-蛋白酶 ; 基因表达 ; 病毒性肝炎 ; 肝细胞癌</subject><ispartof>World journal of gastroenterology : WJG, 2005-04, Vol.11 (16), p.2398-2401</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><rights>2005 Baishideng Publishing Group Inc. All rights reserved. 2005</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-b284f69ec70b21c4dcd6974738b83fa575717c8a8dd0c80c3b2b9d5ea3718fc63</citedby><cites>FETCH-LOGICAL-c450t-b284f69ec70b21c4dcd6974738b83fa575717c8a8dd0c80c3b2b9d5ea3718fc63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305624/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305624/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15832407$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tien, Liem Thanh</creatorcontrib><creatorcontrib>Ito, Masahiro</creatorcontrib><creatorcontrib>Nakao, Mikiko</creatorcontrib><creatorcontrib>Niino, Daisuke</creatorcontrib><creatorcontrib>Serik, Meirmanov</creatorcontrib><creatorcontrib>Nakashima, Masahiro</creatorcontrib><creatorcontrib>Wen, Chun-Yang</creatorcontrib><creatorcontrib>Yatsuhashi, Hiroshi</creatorcontrib><creatorcontrib>Ishibashi, Hiromi</creatorcontrib><title>Expression of β-catenin in hepatocellular carcinoma</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: The β-catenin has been recognized as a critical member of the Wnt signaling pathway and plays an important role in the generation/differentiation of many tissues. Inappropriate activation of this pathway has been implicated in carcinogenesis. The mechanism underlying the development as well as its prognosis of hepatocellular carcinoma (HCC) has remained unclear. The purpose of this study is to analyze the expression of β-catenin in HCC in relation to histological grades and viral hepatitis backgrounds. METHODS: Thirty-two sections were selected at random from autopsy and surgical cases of HCC. Immuohistologically, the location and positivity of β-catenin expression in HCC was examined. RESULTS: Normal hepatocytes did not express β-catenin. In 78% of HCC β-catenin was expressed at the membrane of the cells, with or without cytoplasmic and/or nuclear expression. The tumor cells with well- and moderately-differentiated grades expressed frequently at the membrane and cytoplasm compared with poorly-differentiated type. Nuclear expression of β-catenin was prone to occur in the tumor cells of poorly-differentiated grade. There were 15% of hepatitis C virus (HCV) backgrounds with nuclear expression. In contrast, there was 38% with nuclear expression in hepatitis B virus (HBV) backgrounds. In nonBnonC hepatitis, no case expressed nuclear β-catenin. CONCLUSION: The β-catenin expression in HCC cells was heterogenous among types of hepatitis viral infection. 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Inappropriate activation of this pathway has been implicated in carcinogenesis. The mechanism underlying the development as well as its prognosis of hepatocellular carcinoma (HCC) has remained unclear. The purpose of this study is to analyze the expression of β-catenin in HCC in relation to histological grades and viral hepatitis backgrounds. METHODS: Thirty-two sections were selected at random from autopsy and surgical cases of HCC. Immuohistologically, the location and positivity of β-catenin expression in HCC was examined. RESULTS: Normal hepatocytes did not express β-catenin. In 78% of HCC β-catenin was expressed at the membrane of the cells, with or without cytoplasmic and/or nuclear expression. The tumor cells with well- and moderately-differentiated grades expressed frequently at the membrane and cytoplasm compared with poorly-differentiated type. Nuclear expression of β-catenin was prone to occur in the tumor cells of poorly-differentiated grade. There were 15% of hepatitis C virus (HCV) backgrounds with nuclear expression. In contrast, there was 38% with nuclear expression in hepatitis B virus (HBV) backgrounds. In nonBnonC hepatitis, no case expressed nuclear β-catenin. CONCLUSION: The β-catenin expression in HCC cells was heterogenous among types of hepatitis viral infection. 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identifier ISSN: 1007-9327
ispartof World journal of gastroenterology : WJG, 2005-04, Vol.11 (16), p.2398-2401
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2219-2840
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source MEDLINE; PubMed Central; Alma/SFX Local Collection
subjects Adult
Aged
Aged, 80 and over
beta Catenin
Carcinoma, Hepatocellular - metabolism
Carcinoma, Hepatocellular - pathology
Cytoskeletal Proteins - metabolism
Female
Hepatitis, Viral, Human - metabolism
Hepatitis, Viral, Human - pathology
Humans
Immunohistochemistry
Intercellular Signaling Peptides and Proteins - metabolism
Liver Cancer
Liver Neoplasms - metabolism
Liver Neoplasms - pathology
Male
Middle Aged
Retrospective Studies
Signal Transduction - physiology
Trans-Activators - metabolism
Wnt Proteins
β-蛋白酶
基因表达
病毒性肝炎
肝细胞癌
title Expression of β-catenin in hepatocellular carcinoma
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