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miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor
The epidermal growth factor receptor (EGFR) is frequently activated in a wide range of solid tumours and represents an important therapeutic target. MicroRNAs (miRNAs) have recently been recognized as a rational and potential modality for anti‐EGFR therapies. However, more EGFR‐targeting miRNAs need...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891324/ https://www.ncbi.nlm.nih.gov/pubmed/27241841 http://dx.doi.org/10.1111/jcmm.12889 |
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author | Qin, Qin Wei, Furong Zhang, Jianbo Wang, Xingwu Li, Baosheng |
author_facet | Qin, Qin Wei, Furong Zhang, Jianbo Wang, Xingwu Li, Baosheng |
author_sort | Qin, Qin |
collection | PubMed |
description | The epidermal growth factor receptor (EGFR) is frequently activated in a wide range of solid tumours and represents an important therapeutic target. MicroRNAs (miRNAs) have recently been recognized as a rational and potential modality for anti‐EGFR therapies. However, more EGFR‐targeting miRNAs need to be explored. In this study, we identified a novel EGFR‐targeting miRNA, miRNA‐134 (miR‐134), in non‐small‐cell lung cancer (NSCLC) cell lines. Luciferase assays confirmed that EGFR is a direct target of miR‐134. In addition, the overexpression of miR‐134 inhibited EGFR‐related signaling and suppressed NSCLC cells proliferation by inducing cell cycle arrest and/or apoptosis, suggesting that miR‐134 functions as a tumour suppressor in NSCLC. Further mechanistic investigation including RNAi and rescue experiments suggested that the down‐regulation of EGFR by miR‐134 partially contributes to the antiproliferative role of miR‐134. Last, in vivo experiments demonstrated that miR‐134 suppressed tumour growth of A549 xenograft in nude mice. Taken together, our findings suggest that miR‐134 inhibits non‐small cell lung cancer growth by targeting the EGFR. |
format | Online Article Text |
id | pubmed-4891324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48913242016-10-01 miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor Qin, Qin Wei, Furong Zhang, Jianbo Wang, Xingwu Li, Baosheng J Cell Mol Med Original Articles The epidermal growth factor receptor (EGFR) is frequently activated in a wide range of solid tumours and represents an important therapeutic target. MicroRNAs (miRNAs) have recently been recognized as a rational and potential modality for anti‐EGFR therapies. However, more EGFR‐targeting miRNAs need to be explored. In this study, we identified a novel EGFR‐targeting miRNA, miRNA‐134 (miR‐134), in non‐small‐cell lung cancer (NSCLC) cell lines. Luciferase assays confirmed that EGFR is a direct target of miR‐134. In addition, the overexpression of miR‐134 inhibited EGFR‐related signaling and suppressed NSCLC cells proliferation by inducing cell cycle arrest and/or apoptosis, suggesting that miR‐134 functions as a tumour suppressor in NSCLC. Further mechanistic investigation including RNAi and rescue experiments suggested that the down‐regulation of EGFR by miR‐134 partially contributes to the antiproliferative role of miR‐134. Last, in vivo experiments demonstrated that miR‐134 suppressed tumour growth of A549 xenograft in nude mice. Taken together, our findings suggest that miR‐134 inhibits non‐small cell lung cancer growth by targeting the EGFR. John Wiley and Sons Inc. 2016-05-31 2016-10 /pmc/articles/PMC4891324/ /pubmed/27241841 http://dx.doi.org/10.1111/jcmm.12889 Text en © 2016 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://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 Qin, Qin Wei, Furong Zhang, Jianbo Wang, Xingwu Li, Baosheng miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor |
title | miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor |
title_full | miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor |
title_fullStr | miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor |
title_full_unstemmed | miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor |
title_short | miR‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor |
title_sort | mir‐134 inhibits non‐small cell lung cancer growth by targeting the epidermal growth factor receptor |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891324/ https://www.ncbi.nlm.nih.gov/pubmed/27241841 http://dx.doi.org/10.1111/jcmm.12889 |
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