Effect of GREM[STHZ]1 on the proliferation and metastasis of gastric cancer cells
10.13602/j.cnki.jcls.2019.06.04
- VernacularTitle:GREM1对胃癌细胞增殖迁移的作用
- Author:
Yajing LIN
1
;
Tianjie LI
1
;
Hua WANG
1
;
Shihe SHAO
1
Author Information
1. Jiangsu University School of Medicine
- Publication Type:Journal Article
- Keywords:
GREM1;
gastric cancer;
proliferation;
metastasis;
epithelial-mesenchymal transition
- From:
Chinese Journal of Clinical Laboratory Science
2019;37(6):418-422
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To detect the expression of GREM1 gene in gastric cancer cells, investigate its effects on the biological characteristics of gastric cancer cells and evaluate its application value in the diagnosis and prognosis of gastric cancer.
Methods:The expression difference of GREM1 in gastric cancer tissues and adjacent normal tissues was analyzed by the database, and the correlation of GREM1 expression levels with the prognosis of gastric cancer patients was evaluated. The expression levels of GREM1 protein in gastric cancer cell lines were detected by western blot. After GREM1 gene in AGS cells was silenced, its effects on the proliferation, migration, epithelial-mesenchymal transition (EMT) and Wnt/β-catenin pathway of AGS cells were detected by the colony formation assay, Transwell and Western blot, respectively.
Results:Kaplan-Meier analysis showed that the patients with high expression of GREM1 gene had low overall survival (OS) and progression-free survival (PFS). The expression level of GREM1 protein in AGS cells was the highest in all gastric cancer cell lines (1.967 ± 0.056). The analysis of colony formation assay, Transwell and Western blot showed that the silencing of GREM1 gene could decrease the proliferation and migration of gastric cancer cells (t=22.00; t=29.60; P＜0.01), increase the expression of E-cadherin (t=10.65, P＜0.01), and decrease the expressions of ZEB1 and MMP2 (t=10.74; t=13.67; P＜0.01) and the expressions of β-catenin, Cyclin D1, c-myc, p-GSK3β and PCNA in the Wnt/β-catenin pathway (t=12.65; t=16.21; t=8.74; t=7.75; t=8.42; P＜0.01).
Conclusion:GREM1 may induce EMT by activating the Wnt/β-catenin pathway, [JP2]and promote the metastasis and growth of tumors, which may be used as a new molecular diagnostic and prognostic marker for gastric cancer.
