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miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1
MicroRNAs (miRNAs) have essential roles in carcinogenesis and tumor progression. Here, we investigated the roles and mechanisms of miR-143 in non-small cell lung cancer (NSCLC). miR-143 was significantly decreased in NSCLC tissues and cell lines. Overexpression of miR-143 suppressed NSCLC cell proli...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139824/ https://www.ncbi.nlm.nih.gov/pubmed/25003638 http://dx.doi.org/10.3390/ijms150711973 |
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author | Xia, Hui Sun, Shengjie Wang, Bo Wang, Tao Liang, Chaoyang Li, Guo Huang, Chongbiao Qi, Daliang Chu, Xiangyang |
author_facet | Xia, Hui Sun, Shengjie Wang, Bo Wang, Tao Liang, Chaoyang Li, Guo Huang, Chongbiao Qi, Daliang Chu, Xiangyang |
author_sort | Xia, Hui |
collection | PubMed |
description | MicroRNAs (miRNAs) have essential roles in carcinogenesis and tumor progression. Here, we investigated the roles and mechanisms of miR-143 in non-small cell lung cancer (NSCLC). miR-143 was significantly decreased in NSCLC tissues and cell lines. Overexpression of miR-143 suppressed NSCLC cell proliferation, induced apoptosis, and inhibited migration and invasion in vitro. Integrated analysis identified LIM domain kinase 1 (Limk1) as a direct and functional target of miR-143. Overexpression of Limk1 attenuated the tumor suppressive effects of miR-143 in NSCLC cells. Moreover, miR-143 was inversely correlated with Limk1 expression in NSCLC tissues. Together, our results highlight the significance of miR-143 and Limk1 in the development and progression of NSCLC. |
format | Online Article Text |
id | pubmed-4139824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-41398242014-08-21 miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1 Xia, Hui Sun, Shengjie Wang, Bo Wang, Tao Liang, Chaoyang Li, Guo Huang, Chongbiao Qi, Daliang Chu, Xiangyang Int J Mol Sci Article MicroRNAs (miRNAs) have essential roles in carcinogenesis and tumor progression. Here, we investigated the roles and mechanisms of miR-143 in non-small cell lung cancer (NSCLC). miR-143 was significantly decreased in NSCLC tissues and cell lines. Overexpression of miR-143 suppressed NSCLC cell proliferation, induced apoptosis, and inhibited migration and invasion in vitro. Integrated analysis identified LIM domain kinase 1 (Limk1) as a direct and functional target of miR-143. Overexpression of Limk1 attenuated the tumor suppressive effects of miR-143 in NSCLC cells. Moreover, miR-143 was inversely correlated with Limk1 expression in NSCLC tissues. Together, our results highlight the significance of miR-143 and Limk1 in the development and progression of NSCLC. MDPI 2014-07-07 /pmc/articles/PMC4139824/ /pubmed/25003638 http://dx.doi.org/10.3390/ijms150711973 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Xia, Hui Sun, Shengjie Wang, Bo Wang, Tao Liang, Chaoyang Li, Guo Huang, Chongbiao Qi, Daliang Chu, Xiangyang miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1 |
title | miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1 |
title_full | miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1 |
title_fullStr | miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1 |
title_full_unstemmed | miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1 |
title_short | miR-143 Inhibits NSCLC Cell Growth and Metastasis by Targeting Limk1 |
title_sort | mir-143 inhibits nsclc cell growth and metastasis by targeting limk1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139824/ https://www.ncbi.nlm.nih.gov/pubmed/25003638 http://dx.doi.org/10.3390/ijms150711973 |
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