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Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer

Both the epidermal growth factor receptor signaling pathway and microRNA (miRNA) play an important role in lung cancer development and progression. To address the potential role of miRNA in epidermal growth factor receptor signaling, we identified miR-125a-5p as a downstream target, using an miRNA a...

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Detalles Bibliográficos
Autores principales: Wang, Guofu, Mao, Weimin, Zheng, Shu, Ye, Jingjia
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776928/
https://www.ncbi.nlm.nih.gov/pubmed/19702827
http://dx.doi.org/10.1111/j.1742-4658.2009.07238.x
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author Wang, Guofu
Mao, Weimin
Zheng, Shu
Ye, Jingjia
author_facet Wang, Guofu
Mao, Weimin
Zheng, Shu
Ye, Jingjia
author_sort Wang, Guofu
collection PubMed
description Both the epidermal growth factor receptor signaling pathway and microRNA (miRNA) play an important role in lung cancer development and progression. To address the potential role of miRNA in epidermal growth factor receptor signaling, we identified miR-125a-5p as a downstream target, using an miRNA array. We further demonstrated that miR-125a-5p inhibited migration and invasion of lung cancer cells. Moreover, miR-125a-5p regulated the expression of several downstream genes of epidermal growth factor receptor signaling. Importantly, examination of lung cancer samples revealed a significant correlation of miR-125a-5p repression with lung carcinogenesis. Taken together, our results provide compelling evidence that miR-125a-5p, an epidermal growth factor-signaling-regulated miRNA, may function as a metastatic suppressor.
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spelling pubmed-27769282009-11-21 Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer Wang, Guofu Mao, Weimin Zheng, Shu Ye, Jingjia FEBS J Original Articles Both the epidermal growth factor receptor signaling pathway and microRNA (miRNA) play an important role in lung cancer development and progression. To address the potential role of miRNA in epidermal growth factor receptor signaling, we identified miR-125a-5p as a downstream target, using an miRNA array. We further demonstrated that miR-125a-5p inhibited migration and invasion of lung cancer cells. Moreover, miR-125a-5p regulated the expression of several downstream genes of epidermal growth factor receptor signaling. Importantly, examination of lung cancer samples revealed a significant correlation of miR-125a-5p repression with lung carcinogenesis. Taken together, our results provide compelling evidence that miR-125a-5p, an epidermal growth factor-signaling-regulated miRNA, may function as a metastatic suppressor. Blackwell Publishing Ltd 2009-10 /pmc/articles/PMC2776928/ /pubmed/19702827 http://dx.doi.org/10.1111/j.1742-4658.2009.07238.x Text en Journal compilation © 2009 Federation of European Biochemical Societies http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Wang, Guofu
Mao, Weimin
Zheng, Shu
Ye, Jingjia
Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer
title Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer
title_full Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer
title_fullStr Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer
title_full_unstemmed Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer
title_short Epidermal growth factor receptor-regulated miR-125a-5p – a metastatic inhibitor of lung cancer
title_sort epidermal growth factor receptor-regulated mir-125a-5p – a metastatic inhibitor of lung cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776928/
https://www.ncbi.nlm.nih.gov/pubmed/19702827
http://dx.doi.org/10.1111/j.1742-4658.2009.07238.x
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