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MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma

OBJECTIVE: To investigate the effects of miR-490-3p on the proliferation, migration, invasion and apoptosis of lung adenocarcinoma (LUAD) cells through the Wnt/β-catenin signaling pathway. METHODS: Differentially expressed miRNAs in LUAD tissues were analyzed by bioinformatics and the target miRNA w...

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Autores principales: Li, Zhiyong, Jiang, Danfeng, Yang, Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608555/
https://www.ncbi.nlm.nih.gov/pubmed/33154676
http://dx.doi.org/10.2147/CMAR.S258182
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author Li, Zhiyong
Jiang, Danfeng
Yang, Sheng
author_facet Li, Zhiyong
Jiang, Danfeng
Yang, Sheng
author_sort Li, Zhiyong
collection PubMed
description OBJECTIVE: To investigate the effects of miR-490-3p on the proliferation, migration, invasion and apoptosis of lung adenocarcinoma (LUAD) cells through the Wnt/β-catenin signaling pathway. METHODS: Differentially expressed miRNAs in LUAD tissues were analyzed by bioinformatics and the target miRNA went through GSEA enrichment analysis. qRT-PCR was used to detect the expression of miR-490-3p in human LUAD cells and normal bronchial cells. The constructed vectors were transfected into the LUAD cell lines using Lipofectamine 2000. Cell viability was detected by MTT, cell migration and invasion were detected by transwell assay, and cell apoptosis was detected by flow cytometry. Western blot was performed to detect the expression levels of the proteins related to the Wnt/β-catenin pathway and cell apoptosis. Xenograft tumor mouse models were used for in vivo validation. RESULTS: The results of qRT-PCR showed that miR-490-3p was relatively lowly expressed in LUAD cells, and the expression level was different in different LUAD cell lines. The results of MTT, transwell and flow cytometry exhibited that miR-490-3p could significantly inhibit the proliferation, migration, invasion and increase cell apoptosis rate of LUAD cells. Western blot results showed that miR-490-3p promoted the expression of Bax, Caspase-3 and E-cadherin as well as the phosphorylation of GSK-3β and inhibited the expression of Bcl-2, β-catenin and C-myc. Additionally, animal experiments were performed to prove that miR-490-3p suppressed LUAD malignant progression in vivo. CONCLUSION: MiR-490-3p inhibited the proliferation, migration, invasion and promoted the apoptosis of LUAD cells by down-regulating the Wnt/β-catenin signaling pathway, suggesting that miR-490-3p may be an indicator for early diagnosis and prognosis of LUAD.
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spelling pubmed-76085552020-11-04 MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma Li, Zhiyong Jiang, Danfeng Yang, Sheng Cancer Manag Res Original Research OBJECTIVE: To investigate the effects of miR-490-3p on the proliferation, migration, invasion and apoptosis of lung adenocarcinoma (LUAD) cells through the Wnt/β-catenin signaling pathway. METHODS: Differentially expressed miRNAs in LUAD tissues were analyzed by bioinformatics and the target miRNA went through GSEA enrichment analysis. qRT-PCR was used to detect the expression of miR-490-3p in human LUAD cells and normal bronchial cells. The constructed vectors were transfected into the LUAD cell lines using Lipofectamine 2000. Cell viability was detected by MTT, cell migration and invasion were detected by transwell assay, and cell apoptosis was detected by flow cytometry. Western blot was performed to detect the expression levels of the proteins related to the Wnt/β-catenin pathway and cell apoptosis. Xenograft tumor mouse models were used for in vivo validation. RESULTS: The results of qRT-PCR showed that miR-490-3p was relatively lowly expressed in LUAD cells, and the expression level was different in different LUAD cell lines. The results of MTT, transwell and flow cytometry exhibited that miR-490-3p could significantly inhibit the proliferation, migration, invasion and increase cell apoptosis rate of LUAD cells. Western blot results showed that miR-490-3p promoted the expression of Bax, Caspase-3 and E-cadherin as well as the phosphorylation of GSK-3β and inhibited the expression of Bcl-2, β-catenin and C-myc. Additionally, animal experiments were performed to prove that miR-490-3p suppressed LUAD malignant progression in vivo. CONCLUSION: MiR-490-3p inhibited the proliferation, migration, invasion and promoted the apoptosis of LUAD cells by down-regulating the Wnt/β-catenin signaling pathway, suggesting that miR-490-3p may be an indicator for early diagnosis and prognosis of LUAD. Dove 2020-10-30 /pmc/articles/PMC7608555/ /pubmed/33154676 http://dx.doi.org/10.2147/CMAR.S258182 Text en © 2020 Li et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Li, Zhiyong
Jiang, Danfeng
Yang, Sheng
MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma
title MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma
title_full MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma
title_fullStr MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma
title_full_unstemmed MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma
title_short MiR-490-3p Inhibits the Malignant Progression of Lung Adenocarcinoma
title_sort mir-490-3p inhibits the malignant progression of lung adenocarcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608555/
https://www.ncbi.nlm.nih.gov/pubmed/33154676
http://dx.doi.org/10.2147/CMAR.S258182
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