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High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer

This study analyzed the relationship between several Epstein-Barr virus (EBV) microRNA (miRNA) expression profiles and the clinicopathologic features of patients with EBV-associated gastric cancer. The miRNA expression was examined in 59 tumor and 39 paired normal mucosal tissues from available form...

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Autores principales: Kang, Byung Woog, Choi, YongHun, Kwon, Oh Kyoung, Lee, Seung Soo, Chung, Ho Young, Yu, Wansik, Bae, Han Ik, Seo, An Na, Kang, Hyojeung, Lee, Suk Kyeong, Jeon, Seong Woo, Hur, Keun, Kim, Jong Gwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362460/
https://www.ncbi.nlm.nih.gov/pubmed/28122341
http://dx.doi.org/10.18632/oncotarget.14744
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author Kang, Byung Woog
Choi, YongHun
Kwon, Oh Kyoung
Lee, Seung Soo
Chung, Ho Young
Yu, Wansik
Bae, Han Ik
Seo, An Na
Kang, Hyojeung
Lee, Suk Kyeong
Jeon, Seong Woo
Hur, Keun
Kim, Jong Gwang
author_facet Kang, Byung Woog
Choi, YongHun
Kwon, Oh Kyoung
Lee, Seung Soo
Chung, Ho Young
Yu, Wansik
Bae, Han Ik
Seo, An Na
Kang, Hyojeung
Lee, Suk Kyeong
Jeon, Seong Woo
Hur, Keun
Kim, Jong Gwang
author_sort Kang, Byung Woog
collection PubMed
description This study analyzed the relationship between several Epstein-Barr virus (EBV) microRNA (miRNA) expression profiles and the clinicopathologic features of patients with EBV-associated gastric cancer. The miRNA expression was examined in 59 tumor and 39 paired normal mucosal tissues from available formalin-fixed paraffin embedded tissue samples. The expression levels of miR-BamHI fragment A rightward transcript (BART)1-5p, miR-BART4-5p, and miR-BART20-5p were determined using a quantitative real-time polymerase chain reaction. The expression of all three analyzed EBV microRNAs was significantly higher in the tumor tissue than in the paired normal tissue (P < 0.001 for each). When the median value of the EBV microRNA expression levels was used as the cutoff point, a high BART20-5p expression was associated with worse recurrence-free survival (P = 0.034) in a multivariate analysis including age and pathologic stage. In conclusion, the expression level of BART20-5p may predict recurrence-free survival for patients with EBV-associated gastric cancer. Further studies are warranted to clarify the roles of EBV BART microRNAs in the carcinogenesis, and their potential as a biomarker and therapeutic target for EBV-associated gastric cancer.
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spelling pubmed-53624602017-04-24 High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer Kang, Byung Woog Choi, YongHun Kwon, Oh Kyoung Lee, Seung Soo Chung, Ho Young Yu, Wansik Bae, Han Ik Seo, An Na Kang, Hyojeung Lee, Suk Kyeong Jeon, Seong Woo Hur, Keun Kim, Jong Gwang Oncotarget Research Paper This study analyzed the relationship between several Epstein-Barr virus (EBV) microRNA (miRNA) expression profiles and the clinicopathologic features of patients with EBV-associated gastric cancer. The miRNA expression was examined in 59 tumor and 39 paired normal mucosal tissues from available formalin-fixed paraffin embedded tissue samples. The expression levels of miR-BamHI fragment A rightward transcript (BART)1-5p, miR-BART4-5p, and miR-BART20-5p were determined using a quantitative real-time polymerase chain reaction. The expression of all three analyzed EBV microRNAs was significantly higher in the tumor tissue than in the paired normal tissue (P < 0.001 for each). When the median value of the EBV microRNA expression levels was used as the cutoff point, a high BART20-5p expression was associated with worse recurrence-free survival (P = 0.034) in a multivariate analysis including age and pathologic stage. In conclusion, the expression level of BART20-5p may predict recurrence-free survival for patients with EBV-associated gastric cancer. Further studies are warranted to clarify the roles of EBV BART microRNAs in the carcinogenesis, and their potential as a biomarker and therapeutic target for EBV-associated gastric cancer. Impact Journals LLC 2017-01-19 /pmc/articles/PMC5362460/ /pubmed/28122341 http://dx.doi.org/10.18632/oncotarget.14744 Text en Copyright: © 2017 Kang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Kang, Byung Woog
Choi, YongHun
Kwon, Oh Kyoung
Lee, Seung Soo
Chung, Ho Young
Yu, Wansik
Bae, Han Ik
Seo, An Na
Kang, Hyojeung
Lee, Suk Kyeong
Jeon, Seong Woo
Hur, Keun
Kim, Jong Gwang
High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer
title High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer
title_full High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer
title_fullStr High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer
title_full_unstemmed High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer
title_short High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer
title_sort high level of viral microrna-bart20-5p expression is associated with worse survival of patients with epstein-barr virus-associated gastric cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362460/
https://www.ncbi.nlm.nih.gov/pubmed/28122341
http://dx.doi.org/10.18632/oncotarget.14744
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