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Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer
BACKGROUND: Growing evidence has supported that long non-coding RNAs (lncRNAs) could play vital roles in the development, progression, and prognosis of colorectal cancer (CRC). However, little is known about the clinical significance of BRAF-activated non-coding RNA (BANCR) in CRC. The aim of this s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625712/ https://www.ncbi.nlm.nih.gov/pubmed/28969673 http://dx.doi.org/10.1186/s40659-017-0136-5 |
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author | Shen, Xiaogang Bai, Yifeng Luo, Bin Zhou, Xiaogang |
author_facet | Shen, Xiaogang Bai, Yifeng Luo, Bin Zhou, Xiaogang |
author_sort | Shen, Xiaogang |
collection | PubMed |
description | BACKGROUND: Growing evidence has supported that long non-coding RNAs (lncRNAs) could play vital roles in the development, progression, and prognosis of colorectal cancer (CRC). However, little is known about the clinical significance of BRAF-activated non-coding RNA (BANCR) in CRC. The aim of this study is to explore the clinical value of lncRNA BANCR in CRC patients. METHODS: The expression of lncRNA BANCR was measured in 106 CRC tissues and 65 adjacent normal tissues using the quantitative real-time PCR. RESULTS: The study showed that lncRNA BANCR was highly expressed in CRC tissues compared with adjacent normal tissues (P < 0.001). In addition, high expression of lncRNA BANCR was positively correlated with the lymph node metastasis (P < 0.001). Kaplan–Meier analysis showed that patients with high lncRNA BANCR expression had a shorter overall survival (OS) compared with the low lncRNA BANCR expression group (P = 0.001). Interestingly, for the group of patients with the lymph node metastasis, we found the similar result that high lncRNA BANCR expression was related to poor OS (P = 0.004). Furthermore, the multivariate Cox regression model analysis indicated that high expression of lncRNA BANCR was an independent poor prognostic factor in CRC patients (HR 2.24, 95% CI 1.22–4.16, P = 0.009). CONCLUSIONS: Upregulation of lncRNA BANCR may be associated with the lymph node metastasis and poor survival of CRC. LncRNA BANCR could be served as a novel and useful biomarker for CRC lymph node metastasis and prognosis. |
format | Online Article Text |
id | pubmed-5625712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56257122017-10-12 Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer Shen, Xiaogang Bai, Yifeng Luo, Bin Zhou, Xiaogang Biol Res Research Article BACKGROUND: Growing evidence has supported that long non-coding RNAs (lncRNAs) could play vital roles in the development, progression, and prognosis of colorectal cancer (CRC). However, little is known about the clinical significance of BRAF-activated non-coding RNA (BANCR) in CRC. The aim of this study is to explore the clinical value of lncRNA BANCR in CRC patients. METHODS: The expression of lncRNA BANCR was measured in 106 CRC tissues and 65 adjacent normal tissues using the quantitative real-time PCR. RESULTS: The study showed that lncRNA BANCR was highly expressed in CRC tissues compared with adjacent normal tissues (P < 0.001). In addition, high expression of lncRNA BANCR was positively correlated with the lymph node metastasis (P < 0.001). Kaplan–Meier analysis showed that patients with high lncRNA BANCR expression had a shorter overall survival (OS) compared with the low lncRNA BANCR expression group (P = 0.001). Interestingly, for the group of patients with the lymph node metastasis, we found the similar result that high lncRNA BANCR expression was related to poor OS (P = 0.004). Furthermore, the multivariate Cox regression model analysis indicated that high expression of lncRNA BANCR was an independent poor prognostic factor in CRC patients (HR 2.24, 95% CI 1.22–4.16, P = 0.009). CONCLUSIONS: Upregulation of lncRNA BANCR may be associated with the lymph node metastasis and poor survival of CRC. LncRNA BANCR could be served as a novel and useful biomarker for CRC lymph node metastasis and prognosis. BioMed Central 2017-10-02 /pmc/articles/PMC5625712/ /pubmed/28969673 http://dx.doi.org/10.1186/s40659-017-0136-5 Text en © The Author(s) 2017 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 Article Shen, Xiaogang Bai, Yifeng Luo, Bin Zhou, Xiaogang Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer |
title | Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer |
title_full | Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer |
title_fullStr | Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer |
title_full_unstemmed | Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer |
title_short | Upregulation of lncRNA BANCR associated with the lymph node metastasis and poor prognosis in colorectal cancer |
title_sort | upregulation of lncrna bancr associated with the lymph node metastasis and poor prognosis in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625712/ https://www.ncbi.nlm.nih.gov/pubmed/28969673 http://dx.doi.org/10.1186/s40659-017-0136-5 |
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