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MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma
OBJECTIVE: The aim of this study was to investigate the microRNA-200b-3p expression in lung adenocarcinoma and the possible functional associations of microRNA-200b-3p with cell proliferation, migration, and invasion. METHODS: Quantitative real-time polymerase chain reaction was used to detect the e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893970/ https://www.ncbi.nlm.nih.gov/pubmed/31795847 http://dx.doi.org/10.1177/1533033819892590 |
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author | Liu, Keqiang Zhang, Weiqiang Tan, Jian Ma, Jingbo Zhao, Jing |
author_facet | Liu, Keqiang Zhang, Weiqiang Tan, Jian Ma, Jingbo Zhao, Jing |
author_sort | Liu, Keqiang |
collection | PubMed |
description | OBJECTIVE: The aim of this study was to investigate the microRNA-200b-3p expression in lung adenocarcinoma and the possible functional associations of microRNA-200b-3p with cell proliferation, migration, and invasion. METHODS: Quantitative real-time polymerase chain reaction was used to detect the expression of microRNA-200b-3p in lung adenocarcinoma samples and in the human lung adenocarcinoma cell lines A549 and H1299. A549 and H1299 cells were transfected with either a microRNA-200b-3p mimic or a negative control microRNA or either an empty vector or an adenosine triphosphate-binding cassette transporter A-1 overexpression vector. A Cell Counting Kit-8 assay was employed to assess the ability of cell proliferation. Transwell assays and transwell-Matrigel invasion assay were, respectively, utilized to assess the capacity of migration and invasion in A549 and H1299 cells. RESULTS: The results showed that microRNA-200b-3p expression was significantly upregulated in tumor tissues compared with that in adjacent normal tissues. Overexpression of microRNA-200b-3p promoted lung adenocarcinoma cell proliferation and metastasis. Furthermore, adenosine triphosphate-binding cassette transporter A-1 was a direct target of microRNA-200b-3p, and this binding was verified by luciferase reporter analysis. Overexpression of adenosine triphosphate-binding cassette transporter A-1 obviously suppressed lung adenocarcinoma cell proliferation, migration, and invasion. Lung adenocarcinoma cell phenotypes induced by microRNA-200b-3p overexpression could be partially remitted by the co-overexpression of microRNA-200b-3p and adenosine triphosphate-binding cassette transporter A-1. CONCLUSION: This study first identified that microRNA-200b-3p is upregulated in lung adenocarcinoma cells and associated with cell proliferation and metastasis. MicroRNA-200b-3p promoted lung adenocarcinoma cell proliferation and metastasis by suppressing adenosine triphosphate-binding cassette transporter A-1. MicroRNA-200b-3p may function as a novel molecular marker and therapeutic target for lung adenocarcinoma treatment. |
format | Online Article Text |
id | pubmed-6893970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-68939702019-12-13 MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma Liu, Keqiang Zhang, Weiqiang Tan, Jian Ma, Jingbo Zhao, Jing Technol Cancer Res Treat Original Article OBJECTIVE: The aim of this study was to investigate the microRNA-200b-3p expression in lung adenocarcinoma and the possible functional associations of microRNA-200b-3p with cell proliferation, migration, and invasion. METHODS: Quantitative real-time polymerase chain reaction was used to detect the expression of microRNA-200b-3p in lung adenocarcinoma samples and in the human lung adenocarcinoma cell lines A549 and H1299. A549 and H1299 cells were transfected with either a microRNA-200b-3p mimic or a negative control microRNA or either an empty vector or an adenosine triphosphate-binding cassette transporter A-1 overexpression vector. A Cell Counting Kit-8 assay was employed to assess the ability of cell proliferation. Transwell assays and transwell-Matrigel invasion assay were, respectively, utilized to assess the capacity of migration and invasion in A549 and H1299 cells. RESULTS: The results showed that microRNA-200b-3p expression was significantly upregulated in tumor tissues compared with that in adjacent normal tissues. Overexpression of microRNA-200b-3p promoted lung adenocarcinoma cell proliferation and metastasis. Furthermore, adenosine triphosphate-binding cassette transporter A-1 was a direct target of microRNA-200b-3p, and this binding was verified by luciferase reporter analysis. Overexpression of adenosine triphosphate-binding cassette transporter A-1 obviously suppressed lung adenocarcinoma cell proliferation, migration, and invasion. Lung adenocarcinoma cell phenotypes induced by microRNA-200b-3p overexpression could be partially remitted by the co-overexpression of microRNA-200b-3p and adenosine triphosphate-binding cassette transporter A-1. CONCLUSION: This study first identified that microRNA-200b-3p is upregulated in lung adenocarcinoma cells and associated with cell proliferation and metastasis. MicroRNA-200b-3p promoted lung adenocarcinoma cell proliferation and metastasis by suppressing adenosine triphosphate-binding cassette transporter A-1. MicroRNA-200b-3p may function as a novel molecular marker and therapeutic target for lung adenocarcinoma treatment. SAGE Publications 2019-12-04 /pmc/articles/PMC6893970/ /pubmed/31795847 http://dx.doi.org/10.1177/1533033819892590 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.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 Liu, Keqiang Zhang, Weiqiang Tan, Jian Ma, Jingbo Zhao, Jing MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma |
title | MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma |
title_full | MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma |
title_fullStr | MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma |
title_full_unstemmed | MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma |
title_short | MiR-200b-3p Functions as an Oncogene by Targeting ABCA1 in Lung Adenocarcinoma |
title_sort | mir-200b-3p functions as an oncogene by targeting abca1 in lung adenocarcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893970/ https://www.ncbi.nlm.nih.gov/pubmed/31795847 http://dx.doi.org/10.1177/1533033819892590 |
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