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The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy

Gastrointestinal malignancy is a severe public health threat worldwide, and survival for most types of gastrointestinal cancer is very poor. Therefore, finding better cancer biomarkers to diagnose gastrointestinal malignancy and predict patient survival is essential. HDAC1 has been reported to be cl...

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Autores principales: Cao, Lin-Lin, Yue, Zhihong, Liu, Lianhua, Pei, Lin, Yin, Yue, Qin, Li, Zhao, Jie, Liu, Huixin, Wang, Hui, Jia, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503610/
https://www.ncbi.nlm.nih.gov/pubmed/28424407
http://dx.doi.org/10.18632/oncotarget.16843
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author Cao, Lin-Lin
Yue, Zhihong
Liu, Lianhua
Pei, Lin
Yin, Yue
Qin, Li
Zhao, Jie
Liu, Huixin
Wang, Hui
Jia, Mei
author_facet Cao, Lin-Lin
Yue, Zhihong
Liu, Lianhua
Pei, Lin
Yin, Yue
Qin, Li
Zhao, Jie
Liu, Huixin
Wang, Hui
Jia, Mei
author_sort Cao, Lin-Lin
collection PubMed
description Gastrointestinal malignancy is a severe public health threat worldwide, and survival for most types of gastrointestinal cancer is very poor. Therefore, finding better cancer biomarkers to diagnose gastrointestinal malignancy and predict patient survival is essential. HDAC1 has been reported to be closely associated with several types of cancer, but the precise role of HDAC1 in gastrointestinal cancer is not clear. Recently, quite a few studies have investigated the correlation between HDAC1 expression and clinical features or prognosis in multiple types of gastrointestinal malignancies, but the results were inconsistent. In this study, we systematically reviewed the association between HDAC1 and gastrointestinal malignancy using meta-analysis methods, and 28 eligible studies were analyzed. We found that the expression level of HDAC1 in gastrointestinal malignancies, especially in colorectal cancer (OR = 10.84, 95% CI = 5.33–22.07, P< 0.00001), was higher than that in noncancerous tissue, and HDAC1 expression was closely associated with some clinical features of gastrointestinal cancer patients, such as tumor stage (OR = 1.62, 95% CI = 1.28–2.05, P < 0.0001) and tumor grade (OR = 1.75, 95% CI = 1.03–2.95, P = 0.04). In addition, we also found that patients with low HDAC1 expression showed better overall survival than those with high HDAC1 expression in gastrointestinal malignancy, especially in gastric cancer (HR = 1.88, 95% CI = 1.14–3.12, P = 0.01). Our results strongly suggest that HDAC1 may serve as a good diagnostic and prognostic marker for gastrointestinal malignancy.
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spelling pubmed-55036102017-07-11 The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy Cao, Lin-Lin Yue, Zhihong Liu, Lianhua Pei, Lin Yin, Yue Qin, Li Zhao, Jie Liu, Huixin Wang, Hui Jia, Mei Oncotarget Research Paper Gastrointestinal malignancy is a severe public health threat worldwide, and survival for most types of gastrointestinal cancer is very poor. Therefore, finding better cancer biomarkers to diagnose gastrointestinal malignancy and predict patient survival is essential. HDAC1 has been reported to be closely associated with several types of cancer, but the precise role of HDAC1 in gastrointestinal cancer is not clear. Recently, quite a few studies have investigated the correlation between HDAC1 expression and clinical features or prognosis in multiple types of gastrointestinal malignancies, but the results were inconsistent. In this study, we systematically reviewed the association between HDAC1 and gastrointestinal malignancy using meta-analysis methods, and 28 eligible studies were analyzed. We found that the expression level of HDAC1 in gastrointestinal malignancies, especially in colorectal cancer (OR = 10.84, 95% CI = 5.33–22.07, P< 0.00001), was higher than that in noncancerous tissue, and HDAC1 expression was closely associated with some clinical features of gastrointestinal cancer patients, such as tumor stage (OR = 1.62, 95% CI = 1.28–2.05, P < 0.0001) and tumor grade (OR = 1.75, 95% CI = 1.03–2.95, P = 0.04). In addition, we also found that patients with low HDAC1 expression showed better overall survival than those with high HDAC1 expression in gastrointestinal malignancy, especially in gastric cancer (HR = 1.88, 95% CI = 1.14–3.12, P = 0.01). Our results strongly suggest that HDAC1 may serve as a good diagnostic and prognostic marker for gastrointestinal malignancy. Impact Journals LLC 2017-04-05 /pmc/articles/PMC5503610/ /pubmed/28424407 http://dx.doi.org/10.18632/oncotarget.16843 Text en Copyright: © 2017 Cao et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Cao, Lin-Lin
Yue, Zhihong
Liu, Lianhua
Pei, Lin
Yin, Yue
Qin, Li
Zhao, Jie
Liu, Huixin
Wang, Hui
Jia, Mei
The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy
title The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy
title_full The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy
title_fullStr The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy
title_full_unstemmed The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy
title_short The expression of histone deacetylase HDAC1 correlates with the progression and prognosis of gastrointestinal malignancy
title_sort expression of histone deacetylase hdac1 correlates with the progression and prognosis of gastrointestinal malignancy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503610/
https://www.ncbi.nlm.nih.gov/pubmed/28424407
http://dx.doi.org/10.18632/oncotarget.16843
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