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Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A
BACKGROUND/AIMS: Although LIN28A is known to potentially play a role in the oncogenesis of various cancers, whether LIN28A expression is a predictor of poor prognosis in patients with gastric cancer has not been fully explored. We sought to evaluate clinicopathological characteristics according to t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial Office of Gut and Liver
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003193/ https://www.ncbi.nlm.nih.gov/pubmed/26893371 http://dx.doi.org/10.5009/gnl15283 |
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author | Park, Chan Hyuk Lee, Jung Hwa Lee, Na Keum Lee, Yong Chan Lee, Sang Kil |
author_facet | Park, Chan Hyuk Lee, Jung Hwa Lee, Na Keum Lee, Yong Chan Lee, Sang Kil |
author_sort | Park, Chan Hyuk |
collection | PubMed |
description | BACKGROUND/AIMS: Although LIN28A is known to potentially play a role in the oncogenesis of various cancers, whether LIN28A expression is a predictor of poor prognosis in patients with gastric cancer has not been fully explored. We sought to evaluate clinicopathological characteristics according to the expression of LIN28A in numerous gastric cancer tissue samples. METHODS: LIN28A expression was evaluated by immunohistochemical (IHC) analysis of a tissue microarray comprising 288 gastric cancer tissues and 288 adjacent normal tissues. Clinicopathological characteristics, including overall survival, were compared according to LIN28A expression. RESULTS: The IHC staining score was lower for the cancer tissues than the normal tissues (p<0.001). However, no significant differences were observed in the clinicopathological characteristics between the low and high LIN28A expression groups. In addition, the 5-year overall survival rate did not differ between the two groups: 75.3% (95% confidence interval [CI], 69.3% to 81.7%) versus 71.6% (95% CI, 63.3% to 80.9%) for low versus high expression, respectively. CONCLUSIONS: The expression of LIN28A did not appear to play a distinct role in predicting the clinicopathological characteristics of patients with gastric cancer. In addition, LIN28A expression was not an independently associated factor for overall survival in patients with gastric cancer. |
format | Online Article Text |
id | pubmed-5003193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Editorial Office of Gut and Liver |
record_format | MEDLINE/PubMed |
spelling | pubmed-50031932016-09-09 Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A Park, Chan Hyuk Lee, Jung Hwa Lee, Na Keum Lee, Yong Chan Lee, Sang Kil Gut Liver Original Article BACKGROUND/AIMS: Although LIN28A is known to potentially play a role in the oncogenesis of various cancers, whether LIN28A expression is a predictor of poor prognosis in patients with gastric cancer has not been fully explored. We sought to evaluate clinicopathological characteristics according to the expression of LIN28A in numerous gastric cancer tissue samples. METHODS: LIN28A expression was evaluated by immunohistochemical (IHC) analysis of a tissue microarray comprising 288 gastric cancer tissues and 288 adjacent normal tissues. Clinicopathological characteristics, including overall survival, were compared according to LIN28A expression. RESULTS: The IHC staining score was lower for the cancer tissues than the normal tissues (p<0.001). However, no significant differences were observed in the clinicopathological characteristics between the low and high LIN28A expression groups. In addition, the 5-year overall survival rate did not differ between the two groups: 75.3% (95% confidence interval [CI], 69.3% to 81.7%) versus 71.6% (95% CI, 63.3% to 80.9%) for low versus high expression, respectively. CONCLUSIONS: The expression of LIN28A did not appear to play a distinct role in predicting the clinicopathological characteristics of patients with gastric cancer. In addition, LIN28A expression was not an independently associated factor for overall survival in patients with gastric cancer. Editorial Office of Gut and Liver 2016-09 2016-02-22 /pmc/articles/PMC5003193/ /pubmed/26893371 http://dx.doi.org/10.5009/gnl15283 Text en Copyright © 2016 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Chan Hyuk Lee, Jung Hwa Lee, Na Keum Lee, Yong Chan Lee, Sang Kil Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A |
title | Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A |
title_full | Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A |
title_fullStr | Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A |
title_full_unstemmed | Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A |
title_short | Clinicopathological Characteristics of Patients with Gastric Cancer according to the Expression of LIN28A |
title_sort | clinicopathological characteristics of patients with gastric cancer according to the expression of lin28a |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003193/ https://www.ncbi.nlm.nih.gov/pubmed/26893371 http://dx.doi.org/10.5009/gnl15283 |
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