miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1

Author:

Li Dan12ORCID,Zhang Yunqing3,Li Yulong4,Wang Xiaofei5,Wang Fenghui12,Du Juan12,Zhang Huahua12,Shi Haiyan12,Wang Yanfeng12ORCID,Gao Yi12,Feng Yun12,Yan Jing12,Xue Yajuan12,Yang Yang6ORCID,Zhang Jing12ORCID

Affiliation:

1. Department of Cell Biology and Genetics, Medical College of Yan’an University, Yan’an, 716000 Shaanxi Province, China

2. Yan’an Key Laboratory of Chronic Disease Prevention and Research, Yan’an, 716000 Shaanxi Province, China

3. Laboratory of Obstetrics and Gynecology, Affiliated Hospital of Yan’an University, Yan’an, 716000 Shaanxi Province, China

4. Department of Gastroenterology, Shaanxi Provincial People’s Hospital, Xi’an 710068, China

5. Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi’an Jiaotong University Health Science Center, Xi’an, 710061 Shaanxi, China

6. Department of Toxicology and Sanitary Analysis, School of Public Health, Xi’an Jiaotong University Health Science Center, Xi’an 710061, China

Abstract

Purpose. Gastric cancer is one of the most common cancers in the world. miRNAs play an important role in regulating gene expression by binding with 3 -UTR of the target gene. The aim of this study was to investigate the function of miRNA-149 and FOXC1 in gastric cancer. Patients and Methods. qRT-PCR was used to detect the expression of miRNA-149 and FOXC1 in gastric cancer tissues and cells. Human gastric cancer cell lines AGS and MKN28 were cultured and transfected with miR-149 overexpression plasmid and its control or FOXC1 siRNA and its control. The MTT, colony formation, flow cytometry, wound healing, transwell, and western blotting were performed to examine the function of miRNA-149 and FOXC1 in the development of gastric cancer. What is more, dual-luciferase assay and western blotting were used to demonstrated the relationship between miRNA-149 and FOXC1. Results. miRNA-149 was underexpressed in gastric cancer tissues and cells, while overexpression of miRNA-149 promoted cell apoptosis, retarded cell cycle, and inhibited proliferation and migration in AGS and MKN28 cells. In addition, we showed that miRNA-149 targeted FOXC1. What is more, FOXC1 was highly expressed in gastric cancer tissues and cells; the silencing of FOXC1 inhibited the biological function of AGS and MKN28 cells. Conclusion. miRNA-149 inhibits the biological behavior of gastric cancer by targeting FOXC1, providing a promising target in the treatment of human gastric cancer.

Funder

Yan’an University Scientific Research Projects

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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