Subcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage

Abstract Cholangiocarcinoma (CCA) is a malignant disease with a poor prognosis, and several studies have been conducted using different molecular markers as a tool for CCA diagnosis, including Clonorchis sinensis (CS)-CCA. We initially identified the expression profiles of the three markers of inter...

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Autores principales: Nattawan Suwannakul, Kaoru Midorikawa, Chunping Du, Ya-Peng Qi, Jie Zhang, Bang-De Xiang, Mariko Murata, Ning Ma
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Publicado: Springer 2021
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spelling oai:doaj.org-article:3b6a41d34b9347a18f7791ae260592ff2021-11-14T12:44:39ZSubcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage10.1007/s12672-021-00446-12730-6011https://doaj.org/article/3b6a41d34b9347a18f7791ae260592ff2021-11-01T00:00:00Zhttps://doi.org/10.1007/s12672-021-00446-1https://doaj.org/toc/2730-6011Abstract Cholangiocarcinoma (CCA) is a malignant disease with a poor prognosis, and several studies have been conducted using different molecular markers as a tool for CCA diagnosis, including Clonorchis sinensis (CS)-CCA. We initially identified the expression profiles of the three markers of interest, HMGB1, SOX9, and YAP1, using GSE (GSE76297 and GSE32958) datasets. Upregulated levels of these three proteins were detected in CCA samples compared to those in normal samples. To clarify this issue, 24 human CCA tissues with paired adjacent normal tissues were evaluated using immunohistochemical staining. Of the three markers, the total cellular staining intensities were scanned, and subcellular localization was scored in the nuclear and cytoplasmic regions. The intensities of HMGB1, SOX9, and YAP1 were elevated in CCA tissues than the adjacent normal tissues. Individual scoring of subcellular localization revealed that the expression levels of HMGB1 (nucleus) and YAP1 (nucleus and cytoplasm) were significantly different from the pathologic M stage. Moreover, the translocation pattern was categorized using “site-index”, and the results demonstrated that the overexpression of HMGB1 and SOX9 was mostly observed in both the nucleus and cytoplasm, whereas YAP1 was predominantly expressed in the cytoplasm of tumor cells. Interestingly, the site index of HMGB1 was moderately correlated with the tumor stage (r = 0.441, p = 0.031). These findings imply that the overexpression of subcellular HMGB1 could be associated with the metastatic status of patients with CS-CCA, which was shown to be effective for CS-CCA prognosis.Nattawan SuwannakulKaoru MidorikawaChunping DuYa-Peng QiJie ZhangBang-De XiangMariko MurataNing MaSpringerarticleCholangiocarcinomaSubcellular localizationHMGB1SOX9YAP1Neoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENDiscover Oncology, Vol 12, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Cholangiocarcinoma
Subcellular localization
HMGB1
SOX9
YAP1
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Cholangiocarcinoma
Subcellular localization
HMGB1
SOX9
YAP1
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Nattawan Suwannakul
Kaoru Midorikawa
Chunping Du
Ya-Peng Qi
Jie Zhang
Bang-De Xiang
Mariko Murata
Ning Ma
Subcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage
description Abstract Cholangiocarcinoma (CCA) is a malignant disease with a poor prognosis, and several studies have been conducted using different molecular markers as a tool for CCA diagnosis, including Clonorchis sinensis (CS)-CCA. We initially identified the expression profiles of the three markers of interest, HMGB1, SOX9, and YAP1, using GSE (GSE76297 and GSE32958) datasets. Upregulated levels of these three proteins were detected in CCA samples compared to those in normal samples. To clarify this issue, 24 human CCA tissues with paired adjacent normal tissues were evaluated using immunohistochemical staining. Of the three markers, the total cellular staining intensities were scanned, and subcellular localization was scored in the nuclear and cytoplasmic regions. The intensities of HMGB1, SOX9, and YAP1 were elevated in CCA tissues than the adjacent normal tissues. Individual scoring of subcellular localization revealed that the expression levels of HMGB1 (nucleus) and YAP1 (nucleus and cytoplasm) were significantly different from the pathologic M stage. Moreover, the translocation pattern was categorized using “site-index”, and the results demonstrated that the overexpression of HMGB1 and SOX9 was mostly observed in both the nucleus and cytoplasm, whereas YAP1 was predominantly expressed in the cytoplasm of tumor cells. Interestingly, the site index of HMGB1 was moderately correlated with the tumor stage (r = 0.441, p = 0.031). These findings imply that the overexpression of subcellular HMGB1 could be associated with the metastatic status of patients with CS-CCA, which was shown to be effective for CS-CCA prognosis.
format article
author Nattawan Suwannakul
Kaoru Midorikawa
Chunping Du
Ya-Peng Qi
Jie Zhang
Bang-De Xiang
Mariko Murata
Ning Ma
author_facet Nattawan Suwannakul
Kaoru Midorikawa
Chunping Du
Ya-Peng Qi
Jie Zhang
Bang-De Xiang
Mariko Murata
Ning Ma
author_sort Nattawan Suwannakul
title Subcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage
title_short Subcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage
title_full Subcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage
title_fullStr Subcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage
title_full_unstemmed Subcellular localization of HMGB1 in human cholangiocarcinoma: correlation with tumor stage
title_sort subcellular localization of hmgb1 in human cholangiocarcinoma: correlation with tumor stage
publisher Springer
publishDate 2021
url https://doaj.org/article/3b6a41d34b9347a18f7791ae260592ff
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AT kaorumidorikawa subcellularlocalizationofhmgb1inhumancholangiocarcinomacorrelationwithtumorstage
AT chunpingdu subcellularlocalizationofhmgb1inhumancholangiocarcinomacorrelationwithtumorstage
AT yapengqi subcellularlocalizationofhmgb1inhumancholangiocarcinomacorrelationwithtumorstage
AT jiezhang subcellularlocalizationofhmgb1inhumancholangiocarcinomacorrelationwithtumorstage
AT bangdexiang subcellularlocalizationofhmgb1inhumancholangiocarcinomacorrelationwithtumorstage
AT marikomurata subcellularlocalizationofhmgb1inhumancholangiocarcinomacorrelationwithtumorstage
AT ningma subcellularlocalizationofhmgb1inhumancholangiocarcinomacorrelationwithtumorstage
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