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Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis

Aldo-keto reductase family 1, member B10 (AKR1B10), a cancer-related oxidoreductase, is expressed in well-differentiated hepatocellular carcinomas (HCCs). However, AKR1B10 levels are minimal in normal liver tissues (NLs), similar to the 70-kilodalton heat shock protein (HSP70) and glypican-3. Moreov...

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Autores principales: Tsuzura, Hironori, Genda, Takuya, Sato, Shunsuke, Murata, Ayato, Kanemitsu, Yoshio, Narita, Yutaka, Ishikawa, Sachiko, Kikuchi, Tetsu, Mori, Masashi, Hirano, Katsuharu, Iijima, Katsuyori, Wada, Ryo, Ichida, Takafumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013647/
https://www.ncbi.nlm.nih.gov/pubmed/24747592
http://dx.doi.org/10.3390/ijms15046556
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author Tsuzura, Hironori
Genda, Takuya
Sato, Shunsuke
Murata, Ayato
Kanemitsu, Yoshio
Narita, Yutaka
Ishikawa, Sachiko
Kikuchi, Tetsu
Mori, Masashi
Hirano, Katsuharu
Iijima, Katsuyori
Wada, Ryo
Ichida, Takafumi
author_facet Tsuzura, Hironori
Genda, Takuya
Sato, Shunsuke
Murata, Ayato
Kanemitsu, Yoshio
Narita, Yutaka
Ishikawa, Sachiko
Kikuchi, Tetsu
Mori, Masashi
Hirano, Katsuharu
Iijima, Katsuyori
Wada, Ryo
Ichida, Takafumi
author_sort Tsuzura, Hironori
collection PubMed
description Aldo-keto reductase family 1, member B10 (AKR1B10), a cancer-related oxidoreductase, is expressed in well-differentiated hepatocellular carcinomas (HCCs). However, AKR1B10 levels are minimal in normal liver tissues (NLs), similar to the 70-kilodalton heat shock protein (HSP70) and glypican-3. Moreover, the role of AKR1B10 in chronic hepatitis or cirrhosis, which are considered preneoplastic conditions for HCC, has not been fully elucidated. The aim of this study was to evaluate the expression of AKR1B10, HSP70, and glypican-3 in 61 HCC tissue samples compared to corresponding non-tumorous liver tissues (NTs), comprising 42 chronic hepatitis and 19 cirrhosis cases to clarify the significance of molecular changes at the preneoplastic stages of HCC. Immunohistochemical analysis demonstrated that the median expression levels of AKR1B10 were higher in HCCs than in NTs (p < 0.001) and higher in NTs than NLs (p < 0.001) with 54.8%, 2.1%, and 0.3% expression in HCCs, NTs, and NLs, respectively. HSP70 and glypican-3 were expressed in HCCs, but minimally in NTs and NLs with no significant difference between expression in NTs and NLs. Furthermore, a multivariate analysis identified an association between hepatic steatosis and AKR1B10 expression in NTs (p = 0.020). Of the three protein expressed in well-differentiated HCCs, only AKR1B10 was upregulated in preneoplastic conditions, and a steatosis-related factor might influence its expression.
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spelling pubmed-40136472014-05-08 Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis Tsuzura, Hironori Genda, Takuya Sato, Shunsuke Murata, Ayato Kanemitsu, Yoshio Narita, Yutaka Ishikawa, Sachiko Kikuchi, Tetsu Mori, Masashi Hirano, Katsuharu Iijima, Katsuyori Wada, Ryo Ichida, Takafumi Int J Mol Sci Article Aldo-keto reductase family 1, member B10 (AKR1B10), a cancer-related oxidoreductase, is expressed in well-differentiated hepatocellular carcinomas (HCCs). However, AKR1B10 levels are minimal in normal liver tissues (NLs), similar to the 70-kilodalton heat shock protein (HSP70) and glypican-3. Moreover, the role of AKR1B10 in chronic hepatitis or cirrhosis, which are considered preneoplastic conditions for HCC, has not been fully elucidated. The aim of this study was to evaluate the expression of AKR1B10, HSP70, and glypican-3 in 61 HCC tissue samples compared to corresponding non-tumorous liver tissues (NTs), comprising 42 chronic hepatitis and 19 cirrhosis cases to clarify the significance of molecular changes at the preneoplastic stages of HCC. Immunohistochemical analysis demonstrated that the median expression levels of AKR1B10 were higher in HCCs than in NTs (p < 0.001) and higher in NTs than NLs (p < 0.001) with 54.8%, 2.1%, and 0.3% expression in HCCs, NTs, and NLs, respectively. HSP70 and glypican-3 were expressed in HCCs, but minimally in NTs and NLs with no significant difference between expression in NTs and NLs. Furthermore, a multivariate analysis identified an association between hepatic steatosis and AKR1B10 expression in NTs (p = 0.020). Of the three protein expressed in well-differentiated HCCs, only AKR1B10 was upregulated in preneoplastic conditions, and a steatosis-related factor might influence its expression. Molecular Diversity Preservation International (MDPI) 2014-04-17 /pmc/articles/PMC4013647/ /pubmed/24747592 http://dx.doi.org/10.3390/ijms15046556 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Tsuzura, Hironori
Genda, Takuya
Sato, Shunsuke
Murata, Ayato
Kanemitsu, Yoshio
Narita, Yutaka
Ishikawa, Sachiko
Kikuchi, Tetsu
Mori, Masashi
Hirano, Katsuharu
Iijima, Katsuyori
Wada, Ryo
Ichida, Takafumi
Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis
title Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis
title_full Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis
title_fullStr Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis
title_full_unstemmed Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis
title_short Expression of Aldo-Keto Reductase Family 1 Member B10 in the Early Stages of Human Hepatocarcinogenesis
title_sort expression of aldo-keto reductase family 1 member b10 in the early stages of human hepatocarcinogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013647/
https://www.ncbi.nlm.nih.gov/pubmed/24747592
http://dx.doi.org/10.3390/ijms15046556
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