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Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis

Previously, we reported α(2)-macroglobulin (α(2)M) to be a novel marker characteristic of rat hepatocellular preneoplastic and neoplastic lesions negative for hitherto well-established markers. In the present study, we further examined other candidate markers with specificity for the same type of le...

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Autores principales: Sukata, Tokuo, Uwagawa, Satoshi, Ozaki, Keisuke, Sumida, Kayo, Kushida, Masahiko, Kakehashi, Anna, Wanibuchi, Hideki, Miyata, Kaori, Ogata, Keiko, Fukushima, Shoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Toxicologic Pathology 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234602/
https://www.ncbi.nlm.nih.gov/pubmed/22272003
http://dx.doi.org/10.1293/tox.22.281
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author Sukata, Tokuo
Uwagawa, Satoshi
Ozaki, Keisuke
Sumida, Kayo
Kushida, Masahiko
Kakehashi, Anna
Wanibuchi, Hideki
Miyata, Kaori
Ogata, Keiko
Fukushima, Shoji
author_facet Sukata, Tokuo
Uwagawa, Satoshi
Ozaki, Keisuke
Sumida, Kayo
Kushida, Masahiko
Kakehashi, Anna
Wanibuchi, Hideki
Miyata, Kaori
Ogata, Keiko
Fukushima, Shoji
author_sort Sukata, Tokuo
collection PubMed
description Previously, we reported α(2)-macroglobulin (α(2)M) to be a novel marker characteristic of rat hepatocellular preneoplastic and neoplastic lesions negative for hitherto well-established markers. In the present study, we further examined other candidate markers with specificity for the same type of lesions. Glutathione S-transferase-placental form (GST-P)-negative hepatocellular altered foci (HAF) were generated using a two-stage (initiation and promotion) carcinogenesis protocol with N,N-diethylnitrosamine (DEN) and either Wy-14,643 or clofibrate, two peroxisome proliferators. Microarray analysis using total RNAs isolated from laser-microdissected GST-P-negative HAF (amphophilic cell foci) and adjacent normal tissues was conducted along with immunohistochemistry and real-time RT-PCR. Staining for glucose-regulated protein 78 (GRP78) was detected in GST-P-negative HAF and hepatocellular adenomas, and slightly increased GRP78 mRNA expression was observed in the lesions by real-time RT-PCR analysis. Thus, an early increase of GRP78 expression in hepatocarcinogenesis is likely a feature of the amphophilic subset of HAF.
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spelling pubmed-32346022012-01-23 Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis Sukata, Tokuo Uwagawa, Satoshi Ozaki, Keisuke Sumida, Kayo Kushida, Masahiko Kakehashi, Anna Wanibuchi, Hideki Miyata, Kaori Ogata, Keiko Fukushima, Shoji J Toxicol Pathol Original Previously, we reported α(2)-macroglobulin (α(2)M) to be a novel marker characteristic of rat hepatocellular preneoplastic and neoplastic lesions negative for hitherto well-established markers. In the present study, we further examined other candidate markers with specificity for the same type of lesions. Glutathione S-transferase-placental form (GST-P)-negative hepatocellular altered foci (HAF) were generated using a two-stage (initiation and promotion) carcinogenesis protocol with N,N-diethylnitrosamine (DEN) and either Wy-14,643 or clofibrate, two peroxisome proliferators. Microarray analysis using total RNAs isolated from laser-microdissected GST-P-negative HAF (amphophilic cell foci) and adjacent normal tissues was conducted along with immunohistochemistry and real-time RT-PCR. Staining for glucose-regulated protein 78 (GRP78) was detected in GST-P-negative HAF and hepatocellular adenomas, and slightly increased GRP78 mRNA expression was observed in the lesions by real-time RT-PCR analysis. Thus, an early increase of GRP78 expression in hepatocarcinogenesis is likely a feature of the amphophilic subset of HAF. The Japanese Society of Toxicologic Pathology 2009-12 2009-12-21 /pmc/articles/PMC3234602/ /pubmed/22272003 http://dx.doi.org/10.1293/tox.22.281 Text en 2009 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original
Sukata, Tokuo
Uwagawa, Satoshi
Ozaki, Keisuke
Sumida, Kayo
Kushida, Masahiko
Kakehashi, Anna
Wanibuchi, Hideki
Miyata, Kaori
Ogata, Keiko
Fukushima, Shoji
Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis
title Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis
title_full Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis
title_fullStr Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis
title_full_unstemmed Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis
title_short Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis
title_sort characteristic upregulation of glucose-regulated protein 78 in an early lesion negative for hitherto established cytochemical markers in rat hepatocarcinogenesis
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234602/
https://www.ncbi.nlm.nih.gov/pubmed/22272003
http://dx.doi.org/10.1293/tox.22.281
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