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ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer
ERp29 is a novel endoplasmic reticulum (ER) protein that plays an important role in protein unfolding and secretion. Recently, it has been reported to be widely implicated in control of tumorigenesis in some tumors. However, the potential function of ERp29 in gastric cancer remains poorly understood...
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/PMC5667996/ https://www.ncbi.nlm.nih.gov/pubmed/29108263 http://dx.doi.org/10.18632/oncotarget.20225 |
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author | Wu, Jing Yang, Yuanyan Gao, Shenshen Jiang, Hong Wang, Xin-Qiong Xiao, Yuan Chen, Xue-Hua Li, Pu Xu, Chun-Di |
author_facet | Wu, Jing Yang, Yuanyan Gao, Shenshen Jiang, Hong Wang, Xin-Qiong Xiao, Yuan Chen, Xue-Hua Li, Pu Xu, Chun-Di |
author_sort | Wu, Jing |
collection | PubMed |
description | ERp29 is a novel endoplasmic reticulum (ER) protein that plays an important role in protein unfolding and secretion. Recently, it has been reported to be widely implicated in control of tumorigenesis in some tumors. However, the potential function of ERp29 in gastric cancer remains poorly understood. In this study, we found that the positive rate of ERp29 in gastric cancer tissues was significantly lower than that in adjacent non-tumor tissues. And tumor with high ERp29 expression had inclinations towards smaller tumor size and earlier TNM stage. The in vitro experiments indicated that over-expression of ERp29 in gastric cancer cells significantly suppressed the proliferation and migration of tumor cells, which is consistent with the result of the in vivo animal experiments. Furthermore, our mechanistic investigations revealed that ERp29 reversed EMT process in gastric carcinoma, and its effect was related to the inactivation of ERK1/2 and AKT phosphorylation. Thus, we conclude that ERp29 acts as a tumor suppressor gene in gastric cancer, and is expected to become a novel target of the treatment of GC. |
format | Online Article Text |
id | pubmed-5667996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56679962017-11-04 ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer Wu, Jing Yang, Yuanyan Gao, Shenshen Jiang, Hong Wang, Xin-Qiong Xiao, Yuan Chen, Xue-Hua Li, Pu Xu, Chun-Di Oncotarget Research Paper ERp29 is a novel endoplasmic reticulum (ER) protein that plays an important role in protein unfolding and secretion. Recently, it has been reported to be widely implicated in control of tumorigenesis in some tumors. However, the potential function of ERp29 in gastric cancer remains poorly understood. In this study, we found that the positive rate of ERp29 in gastric cancer tissues was significantly lower than that in adjacent non-tumor tissues. And tumor with high ERp29 expression had inclinations towards smaller tumor size and earlier TNM stage. The in vitro experiments indicated that over-expression of ERp29 in gastric cancer cells significantly suppressed the proliferation and migration of tumor cells, which is consistent with the result of the in vivo animal experiments. Furthermore, our mechanistic investigations revealed that ERp29 reversed EMT process in gastric carcinoma, and its effect was related to the inactivation of ERK1/2 and AKT phosphorylation. Thus, we conclude that ERp29 acts as a tumor suppressor gene in gastric cancer, and is expected to become a novel target of the treatment of GC. Impact Journals LLC 2017-08-12 /pmc/articles/PMC5667996/ /pubmed/29108263 http://dx.doi.org/10.18632/oncotarget.20225 Text en Copyright: © 2017 Wu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wu, Jing Yang, Yuanyan Gao, Shenshen Jiang, Hong Wang, Xin-Qiong Xiao, Yuan Chen, Xue-Hua Li, Pu Xu, Chun-Di ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer |
title | ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer |
title_full | ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer |
title_fullStr | ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer |
title_full_unstemmed | ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer |
title_short | ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer |
title_sort | erp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667996/ https://www.ncbi.nlm.nih.gov/pubmed/29108263 http://dx.doi.org/10.18632/oncotarget.20225 |
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