ERp29 inhibits tumorigenicity by suppressing epithelial mesenchymal transition in gastric cancer

被引:15
|
作者
Wu, Jing [1 ,2 ,3 ]
Yang, Yuanyan [1 ,2 ]
Gao, Shenshen [1 ,2 ,4 ]
Jiang, Hong [3 ]
Wang, Xin-Qiong [1 ,2 ]
Xiao, Yuan [1 ,2 ]
Chen, Xue-Hua [1 ,2 ]
Li, Pu [1 ,2 ]
Xu, Chun-Di [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Pediat, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp North, Shanghai, Peoples R China
[3] Tongji Univ, Sch Med, Dept Oncol, East Hosp, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp North, Dept Human Resource, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
ERp29; EMT; ERK1/2; AKT; gastric cancer; RETICULUM PROTEIN 29; SECRETION FACTOR; BREAST-CANCER; EXPRESSION; METASTASIS; GROWTH; CELLS; AKT;
D O I
10.18632/oncotarget.20225
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:78757 / 78766
页数:10
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