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miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer

Lung cancer is the leading cause of deaths due to cancer. Studies suggest an important role of microRNAs (miRNAs) in a variety of cancers, including lung cancer. In the present study, we evaluated the role of miR-641 in human lung cancer A549 cells. Quantitative RT-PCR and Western blot were used to...

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Detalles Bibliográficos
Autores principales: Kong, Qinglong, Shu, Nan, Li, Jun, Xu, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cognizant Communication Corporation 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844650/
https://www.ncbi.nlm.nih.gov/pubmed/28800790
http://dx.doi.org/10.3727/096504017X15021536183490
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author Kong, Qinglong
Shu, Nan
Li, Jun
Xu, Ning
author_facet Kong, Qinglong
Shu, Nan
Li, Jun
Xu, Ning
author_sort Kong, Qinglong
collection PubMed
description Lung cancer is the leading cause of deaths due to cancer. Studies suggest an important role of microRNAs (miRNAs) in a variety of cancers, including lung cancer. In the present study, we evaluated the role of miR-641 in human lung cancer A549 cells. Quantitative RT-PCR and Western blot were used to measure mRNA and protein expression, respectively. Cell viability and cell apoptosis were respectively measured by MTT assay and flow cytometry. In addition, luciferase activity assay was used to identify the target of miR-641. The expression of miR-641 was downregulated in lung cancer tissues and lung cancer cell lines (p < 0.05 or p < 0.01). Overexpression of miR-641 significantly inhibited proliferation and induced apoptosis of lung cancer cells (p < 0.05, p < 0.01, or p < 0.001). MDM2 was identified as a direct target of miR-641. Overexpression of miR-641 decreased the expression of MDM2 and increased the expression of p53 in lung cancer cells.
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spelling pubmed-78446502021-02-16 miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer Kong, Qinglong Shu, Nan Li, Jun Xu, Ning Oncol Res Article Lung cancer is the leading cause of deaths due to cancer. Studies suggest an important role of microRNAs (miRNAs) in a variety of cancers, including lung cancer. In the present study, we evaluated the role of miR-641 in human lung cancer A549 cells. Quantitative RT-PCR and Western blot were used to measure mRNA and protein expression, respectively. Cell viability and cell apoptosis were respectively measured by MTT assay and flow cytometry. In addition, luciferase activity assay was used to identify the target of miR-641. The expression of miR-641 was downregulated in lung cancer tissues and lung cancer cell lines (p < 0.05 or p < 0.01). Overexpression of miR-641 significantly inhibited proliferation and induced apoptosis of lung cancer cells (p < 0.05, p < 0.01, or p < 0.001). MDM2 was identified as a direct target of miR-641. Overexpression of miR-641 decreased the expression of MDM2 and increased the expression of p53 in lung cancer cells. Cognizant Communication Corporation 2018-06-11 /pmc/articles/PMC7844650/ /pubmed/28800790 http://dx.doi.org/10.3727/096504017X15021536183490 Text en Copyright © 2018 Cognizant, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under a Creative Commons Attribution-NonCommercial NoDerivatives 4.0 International License.
spellingShingle Article
Kong, Qinglong
Shu, Nan
Li, Jun
Xu, Ning
miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer
title miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer
title_full miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer
title_fullStr miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer
title_full_unstemmed miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer
title_short miR-641 Functions as a Tumor Suppressor by Targeting MDM2 in Human Lung Cancer
title_sort mir-641 functions as a tumor suppressor by targeting mdm2 in human lung cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844650/
https://www.ncbi.nlm.nih.gov/pubmed/28800790
http://dx.doi.org/10.3727/096504017X15021536183490
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