Cargando…
Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition
BACKGROUND: Incomplete thermal ablation may induce invasiveness of hepatocellular carcinoma (HCC). Here, we investigated whether activated hepatic stellate cells (HSCs) would accelerate the progression of residual HCC after sublethal heat treatment, and thus sought to identify the potential targets....
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219107/ https://www.ncbi.nlm.nih.gov/pubmed/30400797 http://dx.doi.org/10.1186/s12967-018-1676-3 |
_version_ | 1783368587938889728 |
---|---|
author | Zhang, Rui Lin, Xia-Hui Ma, Min Chen, Jie Chen, Jun Gao, Dong-Mei Cui, Jie-Feng Chen, Rong-Xin |
author_facet | Zhang, Rui Lin, Xia-Hui Ma, Min Chen, Jie Chen, Jun Gao, Dong-Mei Cui, Jie-Feng Chen, Rong-Xin |
author_sort | Zhang, Rui |
collection | PubMed |
description | BACKGROUND: Incomplete thermal ablation may induce invasiveness of hepatocellular carcinoma (HCC). Here, we investigated whether activated hepatic stellate cells (HSCs) would accelerate the progression of residual HCC after sublethal heat treatment, and thus sought to identify the potential targets. METHODS: Hepatocellular carcinoma cells were exposed to sublethal heat treatment and then cultured with the conditioned medium from activated HSCs (HSC-CM). The cell proliferation, migration, invasion and parameters of epithelial–mesenchymal transition (EMT) were analyzed. In vivo tumor progression of heat-treated residual HCC cells inoculated with activated HSCs was studied in nude mice. RESULTS: HSC-CM significantly enhanced the proliferation, motility, invasion, prominent EMT activation and decreased apoptosis of heat-exposed residual HCC cells. These increased malignant phenotypes were markedly attenuated by neutralizing periostin (POSTN) in HSC-CM. Furthermore, exogenous POSTN administration exerted the similar effects of HSC-CM on heat-treated residual HCC cells. POSTN induced the prominent activation of p52Shc and ERK1/2 via integrin β1 in heat-exposed residual HCC cells. Vitamin D analog calcipotriol blocked POSTN secretion from activated HSCs. Calcipotriol plus cisplatin significantly suppressed the activated HSCs-enhanced tumor progression of heat-treated residual HCC cells via the inhibited POSTN expression and the increased apoptosis. CONCLUSIONS: Activated HSCs promote the tumor progression of heat-treated residual HCC through the release of POSTN, which could be inhibited by calcipotriol. Calcipotriol plus cisplatin could be used to thwart the accelerated progression of residual HCC after suboptimal heat treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-018-1676-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6219107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62191072018-11-16 Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition Zhang, Rui Lin, Xia-Hui Ma, Min Chen, Jie Chen, Jun Gao, Dong-Mei Cui, Jie-Feng Chen, Rong-Xin J Transl Med Research BACKGROUND: Incomplete thermal ablation may induce invasiveness of hepatocellular carcinoma (HCC). Here, we investigated whether activated hepatic stellate cells (HSCs) would accelerate the progression of residual HCC after sublethal heat treatment, and thus sought to identify the potential targets. METHODS: Hepatocellular carcinoma cells were exposed to sublethal heat treatment and then cultured with the conditioned medium from activated HSCs (HSC-CM). The cell proliferation, migration, invasion and parameters of epithelial–mesenchymal transition (EMT) were analyzed. In vivo tumor progression of heat-treated residual HCC cells inoculated with activated HSCs was studied in nude mice. RESULTS: HSC-CM significantly enhanced the proliferation, motility, invasion, prominent EMT activation and decreased apoptosis of heat-exposed residual HCC cells. These increased malignant phenotypes were markedly attenuated by neutralizing periostin (POSTN) in HSC-CM. Furthermore, exogenous POSTN administration exerted the similar effects of HSC-CM on heat-treated residual HCC cells. POSTN induced the prominent activation of p52Shc and ERK1/2 via integrin β1 in heat-exposed residual HCC cells. Vitamin D analog calcipotriol blocked POSTN secretion from activated HSCs. Calcipotriol plus cisplatin significantly suppressed the activated HSCs-enhanced tumor progression of heat-treated residual HCC cells via the inhibited POSTN expression and the increased apoptosis. CONCLUSIONS: Activated HSCs promote the tumor progression of heat-treated residual HCC through the release of POSTN, which could be inhibited by calcipotriol. Calcipotriol plus cisplatin could be used to thwart the accelerated progression of residual HCC after suboptimal heat treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-018-1676-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-06 /pmc/articles/PMC6219107/ /pubmed/30400797 http://dx.doi.org/10.1186/s12967-018-1676-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhang, Rui Lin, Xia-Hui Ma, Min Chen, Jie Chen, Jun Gao, Dong-Mei Cui, Jie-Feng Chen, Rong-Xin Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition |
title | Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition |
title_full | Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition |
title_fullStr | Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition |
title_full_unstemmed | Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition |
title_short | Periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition |
title_sort | periostin involved in the activated hepatic stellate cells-induced progression of residual hepatocellular carcinoma after sublethal heat treatment: its role and potential for therapeutic inhibition |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219107/ https://www.ncbi.nlm.nih.gov/pubmed/30400797 http://dx.doi.org/10.1186/s12967-018-1676-3 |
work_keys_str_mv | AT zhangrui periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition AT linxiahui periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition AT mamin periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition AT chenjie periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition AT chenjun periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition AT gaodongmei periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition AT cuijiefeng periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition AT chenrongxin periostininvolvedintheactivatedhepaticstellatecellsinducedprogressionofresidualhepatocellularcarcinomaaftersublethalheattreatmentitsroleandpotentialfortherapeuticinhibition |