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Updated: Oct 8, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1
Dan Li1,2, Yunqing Zhang3, Yulong Li4
1Department of Cell Biology and Genetics, Medical College of Yan'an University, Yan'an, 716000 Shaanxi Province, China.
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.
Insights
MicroRNA-149 (miRNA-149) suppresses gastric cancer progression by targeting FOXC1. Restoring miRNA-149 levels offers a potential therapeutic strategy for gastric cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Gastric cancer is a prevalent malignancy worldwide.
- MicroRNAs (miRNAs) are key regulators of gene expression, impacting various cellular processes.
- Dysregulation of miRNAs is implicated in cancer development and progression.
Purpose of the Study:
- To investigate the functional role of miRNA-149 and FOXC1 in gastric cancer.
- To elucidate the regulatory relationship between miRNA-149 and FOXC1 in gastric cancer cells.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (qRT-PCR) for expression analysis.
- Cell culture, transfection with miRNA-149 overexpression plasmid or FOXC1 siRNA.
- Functional assays including MTT, colony formation, flow cytometry, wound healing, and Transwell assays.
- Dual-luciferase reporter assay and Western blotting to confirm target interaction.
Main Results:
- miRNA-149 was significantly underexpressed in gastric cancer tissues and cell lines.
- Overexpression of miRNA-149 induced apoptosis, cell cycle arrest, and inhibited proliferation and migration.
- miRNA-149 directly targets FOXC1, which was highly expressed in gastric cancer.
- Silencing FOXC1 mimicked the inhibitory effects of miRNA-149 on gastric cancer cell behavior.
Conclusions:
- miRNA-149 acts as a tumor suppressor in gastric cancer by targeting FOXC1.
- The miRNA-149/FOXC1 axis represents a potential therapeutic target for human gastric cancer.
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