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The significance of ENAH in carcinogenesis and prognosis in gastric cancer

The ENAH gene, which encodes a member of the enabled/vasodilator-stimulated phosphoprotein (Ena/VASP) family of proteins, is involved in the assembly of actin filaments required for cell adhesion and motility. Recent studies show overexpressed ENAH in several cancer types, and ENAH correlates with t...

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Autores principales: Wang, Dan-Dan, Jin, Qun, Wang, Lei-Lei, Han, Shu-Fang, Chen, Yi-Bing, Sun, Guo-Dong, Sun, Shi-Fei, Sun, Shu-Wang, Wang, Tao, Liu, Fan-Jie, Wang, Ping, Shi, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641146/
https://www.ncbi.nlm.nih.gov/pubmed/29069803
http://dx.doi.org/10.18632/oncotarget.19801
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author Wang, Dan-Dan
Jin, Qun
Wang, Lei-Lei
Han, Shu-Fang
Chen, Yi-Bing
Sun, Guo-Dong
Sun, Shi-Fei
Sun, Shu-Wang
Wang, Tao
Liu, Fan-Jie
Wang, Ping
Shi, Bin
author_facet Wang, Dan-Dan
Jin, Qun
Wang, Lei-Lei
Han, Shu-Fang
Chen, Yi-Bing
Sun, Guo-Dong
Sun, Shi-Fei
Sun, Shu-Wang
Wang, Tao
Liu, Fan-Jie
Wang, Ping
Shi, Bin
author_sort Wang, Dan-Dan
collection PubMed
description The ENAH gene, which encodes a member of the enabled/vasodilator-stimulated phosphoprotein (Ena/VASP) family of proteins, is involved in the assembly of actin filaments required for cell adhesion and motility. Recent studies show overexpressed ENAH in several cancer types, and ENAH correlates with tumor invasiveness. This study aimed to investigate the expression and function of ENAH in primary gastric adenocarcinoma, and its prognostic significance. We found significantly increased mRNA (P = 0.0283) and protein (P = 0.0301) expression of ENAH in gastric cancer tissues. ENAH expression markedly associated with tumor size (P < 0.001), T stage (P < 0.001), N stage (P = 0.001), TNM stage (P < 0.001) and prognosis (P < 0.001). Cox regression analyses revealed ENAH expression as an independent predictor of overall survival (P = 0.019). We also analyzed data of 155 gastric cancer cases from The Cancer Genome Atlas (TCGA) and found that ENAH expression significantly correlated with age (P = 0.003), T stage (P = 0.023) and prognosis (P = 0.05). Furthermore, the function of ENAH in cell proliferation, colony formation, cell migration and invasion of gastric cancer cells was analyzed in vitro. Knockdown of ENAH expression suppressed cell proliferation, colony formation, cell migration and invasion in MKN45 cells. Conversely, overexpression of ENAH promoted cell proliferation, cell migration and invasion in MGC803 cells. Our research suggests that ENAH might play promoting functions in carcinogenesis and progression of gastric cancer, and may serve as a valuable prognostic marker for primary gastric adenocarcinoma patients.
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spelling pubmed-56411462017-10-24 The significance of ENAH in carcinogenesis and prognosis in gastric cancer Wang, Dan-Dan Jin, Qun Wang, Lei-Lei Han, Shu-Fang Chen, Yi-Bing Sun, Guo-Dong Sun, Shi-Fei Sun, Shu-Wang Wang, Tao Liu, Fan-Jie Wang, Ping Shi, Bin Oncotarget Research Paper The ENAH gene, which encodes a member of the enabled/vasodilator-stimulated phosphoprotein (Ena/VASP) family of proteins, is involved in the assembly of actin filaments required for cell adhesion and motility. Recent studies show overexpressed ENAH in several cancer types, and ENAH correlates with tumor invasiveness. This study aimed to investigate the expression and function of ENAH in primary gastric adenocarcinoma, and its prognostic significance. We found significantly increased mRNA (P = 0.0283) and protein (P = 0.0301) expression of ENAH in gastric cancer tissues. ENAH expression markedly associated with tumor size (P < 0.001), T stage (P < 0.001), N stage (P = 0.001), TNM stage (P < 0.001) and prognosis (P < 0.001). Cox regression analyses revealed ENAH expression as an independent predictor of overall survival (P = 0.019). We also analyzed data of 155 gastric cancer cases from The Cancer Genome Atlas (TCGA) and found that ENAH expression significantly correlated with age (P = 0.003), T stage (P = 0.023) and prognosis (P = 0.05). Furthermore, the function of ENAH in cell proliferation, colony formation, cell migration and invasion of gastric cancer cells was analyzed in vitro. Knockdown of ENAH expression suppressed cell proliferation, colony formation, cell migration and invasion in MKN45 cells. Conversely, overexpression of ENAH promoted cell proliferation, cell migration and invasion in MGC803 cells. Our research suggests that ENAH might play promoting functions in carcinogenesis and progression of gastric cancer, and may serve as a valuable prognostic marker for primary gastric adenocarcinoma patients. Impact Journals LLC 2017-08-02 /pmc/articles/PMC5641146/ /pubmed/29069803 http://dx.doi.org/10.18632/oncotarget.19801 Text en Copyright: © 2017 Wang 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
Wang, Dan-Dan
Jin, Qun
Wang, Lei-Lei
Han, Shu-Fang
Chen, Yi-Bing
Sun, Guo-Dong
Sun, Shi-Fei
Sun, Shu-Wang
Wang, Tao
Liu, Fan-Jie
Wang, Ping
Shi, Bin
The significance of ENAH in carcinogenesis and prognosis in gastric cancer
title The significance of ENAH in carcinogenesis and prognosis in gastric cancer
title_full The significance of ENAH in carcinogenesis and prognosis in gastric cancer
title_fullStr The significance of ENAH in carcinogenesis and prognosis in gastric cancer
title_full_unstemmed The significance of ENAH in carcinogenesis and prognosis in gastric cancer
title_short The significance of ENAH in carcinogenesis and prognosis in gastric cancer
title_sort significance of enah in carcinogenesis and prognosis in gastric cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641146/
https://www.ncbi.nlm.nih.gov/pubmed/29069803
http://dx.doi.org/10.18632/oncotarget.19801
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