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miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value

Micro RNA (miR)-486-5p is often aberrantly expressed in human cancers. The aim of this study was to identify the prognostic value of miR-486-5p expression in digestive system cancers. Tissue microarrays were constructed with 680 samples including 185 esophageal squamous cell carcinomas (ESCCs), 90 g...

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Autores principales: Ren, Chuanli, Chen, Hui, Han, Chongxu, Fu, Deyuan, Zhou, Lin, Jin, Guangfu, Wang, Fuan, Wang, Daxin, Chen, Yong, Ma, Li, Zheng, Xucai, Han, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941281/
https://www.ncbi.nlm.nih.gov/pubmed/26895105
http://dx.doi.org/10.18632/oncotarget.7417
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author Ren, Chuanli
Chen, Hui
Han, Chongxu
Fu, Deyuan
Zhou, Lin
Jin, Guangfu
Wang, Fuan
Wang, Daxin
Chen, Yong
Ma, Li
Zheng, Xucai
Han, Dongsheng
author_facet Ren, Chuanli
Chen, Hui
Han, Chongxu
Fu, Deyuan
Zhou, Lin
Jin, Guangfu
Wang, Fuan
Wang, Daxin
Chen, Yong
Ma, Li
Zheng, Xucai
Han, Dongsheng
author_sort Ren, Chuanli
collection PubMed
description Micro RNA (miR)-486-5p is often aberrantly expressed in human cancers. The aim of this study was to identify the prognostic value of miR-486-5p expression in digestive system cancers. Tissue microarrays were constructed with 680 samples including 185 esophageal squamous cell carcinomas (ESCCs), 90 gastric adenocarcinomas (GCs), and 60 digestive system cancer tissues from 10 ESCC, 10 GC, 10 colon, 10 rectum, 10 liver, 10 pancreatic cancer, and corresponding normal tissues. Twenty normal digestive system mucosa tissues from healthy volunteers were included as normal controls. In GC, miR-486-5p expression was decreased in 62.8% of cases (59/94), increased in 33.0% (31/94), and unchanged in 4.2% (4/94); in ESCC its expression was decreased in 66.2% (129/195), increased in 32.3% (63/195), and unchanged in 1.5% (3/195). Expression of miR-486-5p was decreased in 12, and increased in 8, of 20 cases of colon or rectum cancer; decreased in 6, and increased in 4, of 10 cases of liver cancer; and decreased in 8, and increased in 2, of 10 cases of pancreatic cancer. Multivariate and univariate regression analysis demonstrated that low/unchanged miR-486-5p predicted poor prognosis in ESCC (hazard ratio [HR], 4.32; 95% confidence interval [CI], 2.62–7.14; P < 0.001; HR, 3.88; 95% CI, 2.43–6.22; P < 0.001, respectively) and GC (HR, 2.46; 95% CI, 1.35–4.50; P = 0.003; HR, 2.55; 95% CI, 1.39–4.69; P = 0.002, respectively). MiR-486-5p might therefore be an independent tumor marker for evaluating prognosis in patients with ESCC or GC.
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spelling pubmed-49412812016-07-19 miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value Ren, Chuanli Chen, Hui Han, Chongxu Fu, Deyuan Zhou, Lin Jin, Guangfu Wang, Fuan Wang, Daxin Chen, Yong Ma, Li Zheng, Xucai Han, Dongsheng Oncotarget Research Paper Micro RNA (miR)-486-5p is often aberrantly expressed in human cancers. The aim of this study was to identify the prognostic value of miR-486-5p expression in digestive system cancers. Tissue microarrays were constructed with 680 samples including 185 esophageal squamous cell carcinomas (ESCCs), 90 gastric adenocarcinomas (GCs), and 60 digestive system cancer tissues from 10 ESCC, 10 GC, 10 colon, 10 rectum, 10 liver, 10 pancreatic cancer, and corresponding normal tissues. Twenty normal digestive system mucosa tissues from healthy volunteers were included as normal controls. In GC, miR-486-5p expression was decreased in 62.8% of cases (59/94), increased in 33.0% (31/94), and unchanged in 4.2% (4/94); in ESCC its expression was decreased in 66.2% (129/195), increased in 32.3% (63/195), and unchanged in 1.5% (3/195). Expression of miR-486-5p was decreased in 12, and increased in 8, of 20 cases of colon or rectum cancer; decreased in 6, and increased in 4, of 10 cases of liver cancer; and decreased in 8, and increased in 2, of 10 cases of pancreatic cancer. Multivariate and univariate regression analysis demonstrated that low/unchanged miR-486-5p predicted poor prognosis in ESCC (hazard ratio [HR], 4.32; 95% confidence interval [CI], 2.62–7.14; P < 0.001; HR, 3.88; 95% CI, 2.43–6.22; P < 0.001, respectively) and GC (HR, 2.46; 95% CI, 1.35–4.50; P = 0.003; HR, 2.55; 95% CI, 1.39–4.69; P = 0.002, respectively). MiR-486-5p might therefore be an independent tumor marker for evaluating prognosis in patients with ESCC or GC. Impact Journals LLC 2016-02-16 /pmc/articles/PMC4941281/ /pubmed/26895105 http://dx.doi.org/10.18632/oncotarget.7417 Text en Copyright: © 2016 Ren et al. http://creativecommons.org/licenses/by/2.5/ 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
Ren, Chuanli
Chen, Hui
Han, Chongxu
Fu, Deyuan
Zhou, Lin
Jin, Guangfu
Wang, Fuan
Wang, Daxin
Chen, Yong
Ma, Li
Zheng, Xucai
Han, Dongsheng
miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value
title miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value
title_full miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value
title_fullStr miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value
title_full_unstemmed miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value
title_short miR-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value
title_sort mir-486-5p expression pattern in esophageal squamous cell carcinoma, gastric cancer and its prognostic value
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941281/
https://www.ncbi.nlm.nih.gov/pubmed/26895105
http://dx.doi.org/10.18632/oncotarget.7417
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