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MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma Cells by Targeting AQP4
OBJECTIVE: We aimed to investigate the mechanism of the regulatory axis of miR-196b/AQP4 underlying the invasion and migration of lung adenocarcinoma (LUAD) cells. METHODS: LUAD miRNA and mRNA expression profiles were downloaded from TCGA database and then differential analysis was used to identify...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097310/ https://www.ncbi.nlm.nih.gov/pubmed/33455522 http://dx.doi.org/10.1177/1533033820985868 |
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author | Wu, Xuhui Wu, Gongzhi Zhang, Huaizhong Peng, Xuyang Huang, Bin Huang, Mingjiang Ding, Jianyang Mao, Chaofan Peng, Congxiong |
author_facet | Wu, Xuhui Wu, Gongzhi Zhang, Huaizhong Peng, Xuyang Huang, Bin Huang, Mingjiang Ding, Jianyang Mao, Chaofan Peng, Congxiong |
author_sort | Wu, Xuhui |
collection | PubMed |
description | OBJECTIVE: We aimed to investigate the mechanism of the regulatory axis of miR-196b/AQP4 underlying the invasion and migration of lung adenocarcinoma (LUAD) cells. METHODS: LUAD miRNA and mRNA expression profiles were downloaded from TCGA database and then differential analysis was used to identify the target miRNA. Target gene for the miRNA was obtained via prediction using 3 bioinformatics databases and intersection with the differentially expressed mRNAs searched from TCGA-LUAD. Then, qRT-PCR and western blot were used to validate the expression of miR-196b and AQP4. Dual-luciferase reporter assay was performed to confirm the targeting relationship between miR-196b and AQP4. Transwell assay was used to investigate the migration and invasion of LUAD cells. RESULTS: MiR-196b was screened out by differential and survival analyses, and the downstream target gene AQP4 was identified. In LUAD, miR-196b was highly expressed while AQP4 was poorly expressed. Besides, overexpression of miR-196b promoted cell invasion and migration, while overexpression of AQP4 had negative effects. Moreover, the results of the dual-luciferase reporter assay suggested that AQP4 was a direct target of miR-196b. In addition, we also found that overexpressing AQP4 could suppress the promotive effect of miR-196b on cancer cell invasion and migration. CONCLUSION: MiR-196b promotes the invasion and migration of LUAD cells by down-regulating AQP4, which helps us find new molecular targeted therapies for LUAD. |
format | Online Article Text |
id | pubmed-8097310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-80973102021-05-14 MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma Cells by Targeting AQP4 Wu, Xuhui Wu, Gongzhi Zhang, Huaizhong Peng, Xuyang Huang, Bin Huang, Mingjiang Ding, Jianyang Mao, Chaofan Peng, Congxiong Technol Cancer Res Treat Original Article OBJECTIVE: We aimed to investigate the mechanism of the regulatory axis of miR-196b/AQP4 underlying the invasion and migration of lung adenocarcinoma (LUAD) cells. METHODS: LUAD miRNA and mRNA expression profiles were downloaded from TCGA database and then differential analysis was used to identify the target miRNA. Target gene for the miRNA was obtained via prediction using 3 bioinformatics databases and intersection with the differentially expressed mRNAs searched from TCGA-LUAD. Then, qRT-PCR and western blot were used to validate the expression of miR-196b and AQP4. Dual-luciferase reporter assay was performed to confirm the targeting relationship between miR-196b and AQP4. Transwell assay was used to investigate the migration and invasion of LUAD cells. RESULTS: MiR-196b was screened out by differential and survival analyses, and the downstream target gene AQP4 was identified. In LUAD, miR-196b was highly expressed while AQP4 was poorly expressed. Besides, overexpression of miR-196b promoted cell invasion and migration, while overexpression of AQP4 had negative effects. Moreover, the results of the dual-luciferase reporter assay suggested that AQP4 was a direct target of miR-196b. In addition, we also found that overexpressing AQP4 could suppress the promotive effect of miR-196b on cancer cell invasion and migration. CONCLUSION: MiR-196b promotes the invasion and migration of LUAD cells by down-regulating AQP4, which helps us find new molecular targeted therapies for LUAD. SAGE Publications 2021-01-18 /pmc/articles/PMC8097310/ /pubmed/33455522 http://dx.doi.org/10.1177/1533033820985868 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Wu, Xuhui Wu, Gongzhi Zhang, Huaizhong Peng, Xuyang Huang, Bin Huang, Mingjiang Ding, Jianyang Mao, Chaofan Peng, Congxiong MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma Cells by Targeting AQP4 |
title | MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma
Cells by Targeting AQP4 |
title_full | MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma
Cells by Targeting AQP4 |
title_fullStr | MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma
Cells by Targeting AQP4 |
title_full_unstemmed | MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma
Cells by Targeting AQP4 |
title_short | MiR-196b Promotes the Invasion and Migration of Lung Adenocarcinoma
Cells by Targeting AQP4 |
title_sort | mir-196b promotes the invasion and migration of lung adenocarcinoma
cells by targeting aqp4 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097310/ https://www.ncbi.nlm.nih.gov/pubmed/33455522 http://dx.doi.org/10.1177/1533033820985868 |
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