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Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma

BACKGROUND: Long noncoding RNAs (lncRNAs) have been proved to play important roles in the tumorigenesis and development of human hepatocellular carcinoma (HCC). The aim of our study is to investigate the expression and function of BRAF-activated noncoding RNA (BANCR) in HCC. METHODS: BANCR expressio...

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Autores principales: Zhou, Tao, Gao, Yanjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709863/
https://www.ncbi.nlm.nih.gov/pubmed/26758762
http://dx.doi.org/10.1186/s12957-015-0757-5
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author Zhou, Tao
Gao, Yanjing
author_facet Zhou, Tao
Gao, Yanjing
author_sort Zhou, Tao
collection PubMed
description BACKGROUND: Long noncoding RNAs (lncRNAs) have been proved to play important roles in the tumorigenesis and development of human hepatocellular carcinoma (HCC). The aim of our study is to investigate the expression and function of BRAF-activated noncoding RNA (BANCR) in HCC. METHODS: BANCR expression was detected in HCC tissues and cell lines by using quantitative real-time PCR (qRT-PCR). Association between BANCR levels and clinicopathological factors and patient prognosis was also analyzed. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT), flow cytometry, and transwell invasion and migration assays were used to investigate the role of BANCR in the regulation of biological behaviors of HCC cells. RESULTS: BANCR expression was remarkably increased in HCC tissues compared with adjacent noncancerous tissues (P < 0.001). BANCR expression in four HCC cell lines was also significantly upregulated (P < 0.05). Clinicopathologic analysis revealed that high BANCR expression correlated with high tumor grade, large tumor size, venous infiltration, advanced tumor, node, and metastasis (TNM) stage, and shorter overall survival. Multivariate regression analysis identified BANCR overexpression as an independent unfavorable prognostic factor (relative risk [RR] 4.245; P = 0.015) in HCC patients. Moreover, BANCR downregulation in Hep3B cells impaired cell proliferation, promoted cell apoptosis, reduced cell invasion and migration, led to downregulated vimentin, and upregulated E-cadherin protein levels. CONCLUSIONS: These findings suggested that BANCR may contribute to HCC initiation and progression and would be used as not only a novel prognostic marker but also a potential therapeutic target for this disease.
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spelling pubmed-47098632016-01-13 Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma Zhou, Tao Gao, Yanjing World J Surg Oncol Research BACKGROUND: Long noncoding RNAs (lncRNAs) have been proved to play important roles in the tumorigenesis and development of human hepatocellular carcinoma (HCC). The aim of our study is to investigate the expression and function of BRAF-activated noncoding RNA (BANCR) in HCC. METHODS: BANCR expression was detected in HCC tissues and cell lines by using quantitative real-time PCR (qRT-PCR). Association between BANCR levels and clinicopathological factors and patient prognosis was also analyzed. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT), flow cytometry, and transwell invasion and migration assays were used to investigate the role of BANCR in the regulation of biological behaviors of HCC cells. RESULTS: BANCR expression was remarkably increased in HCC tissues compared with adjacent noncancerous tissues (P < 0.001). BANCR expression in four HCC cell lines was also significantly upregulated (P < 0.05). Clinicopathologic analysis revealed that high BANCR expression correlated with high tumor grade, large tumor size, venous infiltration, advanced tumor, node, and metastasis (TNM) stage, and shorter overall survival. Multivariate regression analysis identified BANCR overexpression as an independent unfavorable prognostic factor (relative risk [RR] 4.245; P = 0.015) in HCC patients. Moreover, BANCR downregulation in Hep3B cells impaired cell proliferation, promoted cell apoptosis, reduced cell invasion and migration, led to downregulated vimentin, and upregulated E-cadherin protein levels. CONCLUSIONS: These findings suggested that BANCR may contribute to HCC initiation and progression and would be used as not only a novel prognostic marker but also a potential therapeutic target for this disease. BioMed Central 2016-01-12 /pmc/articles/PMC4709863/ /pubmed/26758762 http://dx.doi.org/10.1186/s12957-015-0757-5 Text en © Zhou and Gao. 2016 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
Zhou, Tao
Gao, Yanjing
Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma
title Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma
title_full Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma
title_fullStr Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma
title_full_unstemmed Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma
title_short Increased expression of LncRNA BANCR and its prognostic significance in human hepatocellular carcinoma
title_sort increased expression of lncrna bancr and its prognostic significance in human hepatocellular carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709863/
https://www.ncbi.nlm.nih.gov/pubmed/26758762
http://dx.doi.org/10.1186/s12957-015-0757-5
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