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miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer

BACKGROUND: Lung cancer is one of the most common malignant tumors threatening human health. The aim of this study was to investigate the function of miR‐21‐5p in lung cancer progression. METHODS: We analyzed the expression levels of miR‐21‐5p in lung cancer tissues and cell lines. The qRT‐PCR and M...

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Detalles Bibliográficos
Autores principales: Tang, Jinming, Li, Xu, Cheng, Tianli, Wu, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410517/
https://www.ncbi.nlm.nih.gov/pubmed/34254453
http://dx.doi.org/10.1111/1759-7714.14060
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author Tang, Jinming
Li, Xu
Cheng, Tianli
Wu, Jie
author_facet Tang, Jinming
Li, Xu
Cheng, Tianli
Wu, Jie
author_sort Tang, Jinming
collection PubMed
description BACKGROUND: Lung cancer is one of the most common malignant tumors threatening human health. The aim of this study was to investigate the function of miR‐21‐5p in lung cancer progression. METHODS: We analyzed the expression levels of miR‐21‐5p in lung cancer tissues and cell lines. The qRT‐PCR and MTT assays were performed after transfection with miR‐21‐5p mimic, inhibitor and negative control into lung cancer cells. RESULTS: Luciferase reporter assays showed miR‐21‐5p directly target SMAD7. The miR‐21‐5p inhibitor significantly suppressed lung cancer cell proliferation, invasion and migration. We found that SMAD7 was upregulated in lung cancer tissue. In addition, we found that SMAD7 inhibited lung cancer cell proliferation and miR‐21‐5p mimic damaged the inhibitory effect of SMAD7. CONCLUSIONS: miRNA‐21‐5p may promote cell proliferation, migration and invasion by spoiling SMAD7 expression in lung cancer cells.
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spelling pubmed-84105172021-09-03 miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer Tang, Jinming Li, Xu Cheng, Tianli Wu, Jie Thorac Cancer Original Articles BACKGROUND: Lung cancer is one of the most common malignant tumors threatening human health. The aim of this study was to investigate the function of miR‐21‐5p in lung cancer progression. METHODS: We analyzed the expression levels of miR‐21‐5p in lung cancer tissues and cell lines. The qRT‐PCR and MTT assays were performed after transfection with miR‐21‐5p mimic, inhibitor and negative control into lung cancer cells. RESULTS: Luciferase reporter assays showed miR‐21‐5p directly target SMAD7. The miR‐21‐5p inhibitor significantly suppressed lung cancer cell proliferation, invasion and migration. We found that SMAD7 was upregulated in lung cancer tissue. In addition, we found that SMAD7 inhibited lung cancer cell proliferation and miR‐21‐5p mimic damaged the inhibitory effect of SMAD7. CONCLUSIONS: miRNA‐21‐5p may promote cell proliferation, migration and invasion by spoiling SMAD7 expression in lung cancer cells. John Wiley & Sons Australia, Ltd 2021-07-12 2021-09 /pmc/articles/PMC8410517/ /pubmed/34254453 http://dx.doi.org/10.1111/1759-7714.14060 Text en © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Tang, Jinming
Li, Xu
Cheng, Tianli
Wu, Jie
miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer
title miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer
title_full miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer
title_fullStr miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer
title_full_unstemmed miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer
title_short miR‐21‐5p/SMAD7 axis promotes the progress of lung cancer
title_sort mir‐21‐5p/smad7 axis promotes the progress of lung cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410517/
https://www.ncbi.nlm.nih.gov/pubmed/34254453
http://dx.doi.org/10.1111/1759-7714.14060
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