Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastoma

<b>Objective</b> The aim of the present study was to analyze the prognostic factors in patients with hepatoblastoma (HB) in our single center and to evaluate periostin (POSTN) expression in HB and its association with clinicopathological variables. In addition, the underlying mechanism o...

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Main Authors: Lu Chen, Xiangdong Tian, Wenchen Gong, Bo Sun, Guangtao Li, Dongming Liu, Piao Guo, Yuchao He, Ziye Chen, Yuren Xia, Tianqiang Song, Hua Guo
Format: Article
Language:English
Published: China Anti-Cancer Association 2019-03-01
Series:Cancer Biology & Medicine
Subjects:
EMT
Online Access:http://www.cancerbiomed.org/index.php/cocr/article/view/1347
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record_format Article
collection DOAJ
language English
format Article
sources DOAJ
author Lu Chen
Xiangdong Tian
Wenchen Gong
Bo Sun
Guangtao Li
Dongming Liu
Piao Guo
Yuchao He
Ziye Chen
Yuren Xia
Tianqiang Song
Hua Guo
spellingShingle Lu Chen
Xiangdong Tian
Wenchen Gong
Bo Sun
Guangtao Li
Dongming Liu
Piao Guo
Yuchao He
Ziye Chen
Yuren Xia
Tianqiang Song
Hua Guo
Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastoma
Cancer Biology & Medicine
Periostin
hepatoblastoma
EMT
MAPK/ERK
author_facet Lu Chen
Xiangdong Tian
Wenchen Gong
Bo Sun
Guangtao Li
Dongming Liu
Piao Guo
Yuchao He
Ziye Chen
Yuren Xia
Tianqiang Song
Hua Guo
author_sort Lu Chen
title Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastoma
title_short Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastoma
title_full Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastoma
title_fullStr Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastoma
title_full_unstemmed Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastoma
title_sort periostin mediates epithelial-mesenchymal transition through the mapk/erk pathway in hepatoblastoma
publisher China Anti-Cancer Association
series Cancer Biology & Medicine
issn 2095-3941
2095-3941
publishDate 2019-03-01
description <b>Objective</b> The aim of the present study was to analyze the prognostic factors in patients with hepatoblastoma (HB) in our single center and to evaluate periostin (POSTN) expression in HB and its association with clinicopathological variables. In addition, the underlying mechanism of how POSTN promotes HB progression was discussed.<b>Methods</b> POSTN expression was investigated in HB tumors by immunohistochemistry (IHC), immunofluorescence (IF) and Western blot (WB). The association among POSTN expression, clinicopathological features and overall survival (OS) was also evaluated. The migration and adhesion ability of HB cells were measured using chemotaxis and cell-matrix adhesion assays, respectively. Epithelial-mesenchymal transition (EMT)-associated markers and activation of the ERK pathway were detected by WB.<b>Results</b> HB patients had poor prognosis which displayed lymph node metastasis, vascular invasion, POSTN and vimentin expression. POSTN expression was also associated with lymph node metastasis. Furthermore, overexpressed POSTN promoted migration and the adhesive ability of HB cells <i>in vitro</i>. In addition, we demonstrated that POSTN activated the MAPK/ERK pathway, upregulated the expression of Snail and decreased the expression of OVOL2. Finally, POSTN promoted the expression of EMT-associated markers.<b>Conclusions</b> POSTN might modulate EMT via the ERK signaling pathway, thereby promoting cellular migration and invasion. Our study also suggests that POSTN may serve as a therapeutic biomarker in HB patients.
topic Periostin
hepatoblastoma
EMT
MAPK/ERK
url http://www.cancerbiomed.org/index.php/cocr/article/view/1347
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spelling doaj-167922c4366342f7bacf234368dc3d642020-11-24T21:49:56ZengChina Anti-Cancer AssociationCancer Biology & Medicine2095-39412095-39412019-03-011618910010.20892/j.issn.2095-3941.2018.00772018000077Periostin mediates epithelial-mesenchymal transition through the MAPK/ERK pathway in hepatoblastomaLu ChenXiangdong TianWenchen Gong0Bo Sun1Guangtao Li2Dongming Liu3Piao Guo4Yuchao He5Ziye Chen6Yuren Xia7Tianqiang Song8Hua Guo9Department of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, ChinaDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, China<b>Objective</b> The aim of the present study was to analyze the prognostic factors in patients with hepatoblastoma (HB) in our single center and to evaluate periostin (POSTN) expression in HB and its association with clinicopathological variables. In addition, the underlying mechanism of how POSTN promotes HB progression was discussed.<b>Methods</b> POSTN expression was investigated in HB tumors by immunohistochemistry (IHC), immunofluorescence (IF) and Western blot (WB). The association among POSTN expression, clinicopathological features and overall survival (OS) was also evaluated. The migration and adhesion ability of HB cells were measured using chemotaxis and cell-matrix adhesion assays, respectively. Epithelial-mesenchymal transition (EMT)-associated markers and activation of the ERK pathway were detected by WB.<b>Results</b> HB patients had poor prognosis which displayed lymph node metastasis, vascular invasion, POSTN and vimentin expression. POSTN expression was also associated with lymph node metastasis. Furthermore, overexpressed POSTN promoted migration and the adhesive ability of HB cells <i>in vitro</i>. In addition, we demonstrated that POSTN activated the MAPK/ERK pathway, upregulated the expression of Snail and decreased the expression of OVOL2. Finally, POSTN promoted the expression of EMT-associated markers.<b>Conclusions</b> POSTN might modulate EMT via the ERK signaling pathway, thereby promoting cellular migration and invasion. Our study also suggests that POSTN may serve as a therapeutic biomarker in HB patients.http://www.cancerbiomed.org/index.php/cocr/article/view/1347PeriostinhepatoblastomaEMTMAPK/ERK