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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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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. |
format | Online Article Text |
id | pubmed-5641146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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