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miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1
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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709748/ https://www.ncbi.nlm.nih.gov/pubmed/34957298 http://dx.doi.org/10.1155/2021/1503403 |
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author | Li, Dan Zhang, Yunqing Li, Yulong Wang, Xiaofei Wang, Fenghui Du, Juan Zhang, Huahua Shi, Haiyan Wang, Yanfeng Gao, Yi Feng, Yun Yan, Jing Xue, Yajuan Yang, Yang Zhang, Jing |
author_facet | Li, Dan Zhang, Yunqing Li, Yulong Wang, Xiaofei Wang, Fenghui Du, Juan Zhang, Huahua Shi, Haiyan Wang, Yanfeng Gao, Yi Feng, Yun Yan, Jing Xue, Yajuan Yang, Yang Zhang, Jing |
author_sort | Li, Dan |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8709748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-87097482021-12-25 miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1 Li, Dan Zhang, Yunqing Li, Yulong Wang, Xiaofei Wang, Fenghui Du, Juan Zhang, Huahua Shi, Haiyan Wang, Yanfeng Gao, Yi Feng, Yun Yan, Jing Xue, Yajuan Yang, Yang Zhang, Jing Biomed Res Int Research Article 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. Hindawi 2021-12-17 /pmc/articles/PMC8709748/ /pubmed/34957298 http://dx.doi.org/10.1155/2021/1503403 Text en Copyright © 2021 Dan Li et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Dan Zhang, Yunqing Li, Yulong Wang, Xiaofei Wang, Fenghui Du, Juan Zhang, Huahua Shi, Haiyan Wang, Yanfeng Gao, Yi Feng, Yun Yan, Jing Xue, Yajuan Yang, Yang Zhang, Jing miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1 |
title | miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1 |
title_full | miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1 |
title_fullStr | miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1 |
title_full_unstemmed | miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1 |
title_short | miR-149 Suppresses the Proliferation and Metastasis of Human Gastric Cancer Cells by Targeting FOXC1 |
title_sort | mir-149 suppresses the proliferation and metastasis of human gastric cancer cells by targeting foxc1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709748/ https://www.ncbi.nlm.nih.gov/pubmed/34957298 http://dx.doi.org/10.1155/2021/1503403 |
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