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Lrig1 is a positive prognostic marker in hepatocellular carcinoma

BACKGROUND: The prevalence of hepatocellular carcinoma (HCC) is increasing worldwide. As a consequence, there is an urgent need for identifying molecular markers of HCC development and progression. Recently, several studies have suggested that the Lrig1 may have prognostic implications in various ca...

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Autores principales: Yang, Bo, Dai, Chen, Tan, Rumeng, Zhang, Bo, Meng, Xiao, Ye, Jing, Wang, Xinqiang, Wei, Lai, He, Fan, Chen, Zhishui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117876/
https://www.ncbi.nlm.nih.gov/pubmed/27895499
http://dx.doi.org/10.2147/OTT.S112534
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author Yang, Bo
Dai, Chen
Tan, Rumeng
Zhang, Bo
Meng, Xiao
Ye, Jing
Wang, Xinqiang
Wei, Lai
He, Fan
Chen, Zhishui
author_facet Yang, Bo
Dai, Chen
Tan, Rumeng
Zhang, Bo
Meng, Xiao
Ye, Jing
Wang, Xinqiang
Wei, Lai
He, Fan
Chen, Zhishui
author_sort Yang, Bo
collection PubMed
description BACKGROUND: The prevalence of hepatocellular carcinoma (HCC) is increasing worldwide. As a consequence, there is an urgent need for identifying molecular markers of HCC development and progression. Recently, several studies have suggested that the Lrig1 may have prognostic implications in various cancer types, but its clinical value in HCC is not well evaluated. MATERIALS AND METHODS: In this study, the expression level of Lrig1 was examined in 133 HCC tissues and adjacent normal tissues by immunohistochemistry. Furthermore, potential associations between Lrig1 expression and the carcinoma clinical parameters were investigated, including recurrence and survival rate. We silenced the Lrig1 in the normal liver cell line (LO2) and liver cancer cell line (Hep-G2) in vitro by the small interference RNA and detected its influence on proliferation, migration, and invasion. RESULTS: The expression of Lrig1 was significantly downregulated in liver cancer tissues and cell lines, and its expression levels were related to tumor size, tumor–node–metastasis staging and tumor recurrence. Furthermore, analysis of 6-year survival of 133 HCC patients showed that those with stronger Lrig1 expression had significantly longer overall survival time than those with weaker Lrig1 expression. In addition, decreased expression of Lrig1 in vitro promoted the growth, migration, or invasion of normal liver cells and cancer cells. CONCLUSION: Our findings demonstrate that Lrig1 could serve as a potential marker in the prognosis of patients with HCC. We also revealed that Lrig1 might be involved in the metastatic progression of liver cancer. However, its clinical value should be further investigated in the future.
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spelling pubmed-51178762016-11-28 Lrig1 is a positive prognostic marker in hepatocellular carcinoma Yang, Bo Dai, Chen Tan, Rumeng Zhang, Bo Meng, Xiao Ye, Jing Wang, Xinqiang Wei, Lai He, Fan Chen, Zhishui Onco Targets Ther Original Research BACKGROUND: The prevalence of hepatocellular carcinoma (HCC) is increasing worldwide. As a consequence, there is an urgent need for identifying molecular markers of HCC development and progression. Recently, several studies have suggested that the Lrig1 may have prognostic implications in various cancer types, but its clinical value in HCC is not well evaluated. MATERIALS AND METHODS: In this study, the expression level of Lrig1 was examined in 133 HCC tissues and adjacent normal tissues by immunohistochemistry. Furthermore, potential associations between Lrig1 expression and the carcinoma clinical parameters were investigated, including recurrence and survival rate. We silenced the Lrig1 in the normal liver cell line (LO2) and liver cancer cell line (Hep-G2) in vitro by the small interference RNA and detected its influence on proliferation, migration, and invasion. RESULTS: The expression of Lrig1 was significantly downregulated in liver cancer tissues and cell lines, and its expression levels were related to tumor size, tumor–node–metastasis staging and tumor recurrence. Furthermore, analysis of 6-year survival of 133 HCC patients showed that those with stronger Lrig1 expression had significantly longer overall survival time than those with weaker Lrig1 expression. In addition, decreased expression of Lrig1 in vitro promoted the growth, migration, or invasion of normal liver cells and cancer cells. CONCLUSION: Our findings demonstrate that Lrig1 could serve as a potential marker in the prognosis of patients with HCC. We also revealed that Lrig1 might be involved in the metastatic progression of liver cancer. However, its clinical value should be further investigated in the future. Dove Medical Press 2016-11-15 /pmc/articles/PMC5117876/ /pubmed/27895499 http://dx.doi.org/10.2147/OTT.S112534 Text en © 2016 Yang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yang, Bo
Dai, Chen
Tan, Rumeng
Zhang, Bo
Meng, Xiao
Ye, Jing
Wang, Xinqiang
Wei, Lai
He, Fan
Chen, Zhishui
Lrig1 is a positive prognostic marker in hepatocellular carcinoma
title Lrig1 is a positive prognostic marker in hepatocellular carcinoma
title_full Lrig1 is a positive prognostic marker in hepatocellular carcinoma
title_fullStr Lrig1 is a positive prognostic marker in hepatocellular carcinoma
title_full_unstemmed Lrig1 is a positive prognostic marker in hepatocellular carcinoma
title_short Lrig1 is a positive prognostic marker in hepatocellular carcinoma
title_sort lrig1 is a positive prognostic marker in hepatocellular carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117876/
https://www.ncbi.nlm.nih.gov/pubmed/27895499
http://dx.doi.org/10.2147/OTT.S112534
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