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miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma
MicroRNAs (miRNAs) are key regulators of multiple cancers, including non-small cell lung carcinoma (NSCLC). The aim of this study was to determine the expression pattern of miR-769-5p in NSCLC and to investigate its biological role during tumorigenesis. We showed that miR-769-5p was significantly do...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768346/ https://www.ncbi.nlm.nih.gov/pubmed/29371929 http://dx.doi.org/10.18632/oncotarget.23060 |
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author | Yang, Zhao He, Jin Gao, Peng Niu, Yi Zhang, Jie Wang, Lei Liu, Meiyue Wei, Xiaomei Liu, Chunling Zhang, Chao Wang, Wei Du, Jiayi Li, Hongmin Hu, Wanning Sun, Guogui |
author_facet | Yang, Zhao He, Jin Gao, Peng Niu, Yi Zhang, Jie Wang, Lei Liu, Meiyue Wei, Xiaomei Liu, Chunling Zhang, Chao Wang, Wei Du, Jiayi Li, Hongmin Hu, Wanning Sun, Guogui |
author_sort | Yang, Zhao |
collection | PubMed |
description | MicroRNAs (miRNAs) are key regulators of multiple cancers, including non-small cell lung carcinoma (NSCLC). The aim of this study was to determine the expression pattern of miR-769-5p in NSCLC and to investigate its biological role during tumorigenesis. We showed that miR-769-5p was significantly downregulated and predicted poor prognosis in NSCLC compared with corresponding normal tissues. We then investigated its function and found that miR-769-5p significantly inhibited cell proliferation, migration and invasion in vitro and reduced tumor growth and metastasis in vivo. Furthermore, we explored the molecular mechanisms by which miR-769-5p contributes to NSCLC suppression and identified TGFBR1 as a direct target gene of miR-769-5p. Finally, we showed that TGFBR1 had opposite effects to those of miR-769-5p on lung cancer cells, suggesting that miR-769-5p might inhibit lung tumorigenesis by silencing TGFBR1. Taken together, our results demonstrated that miR-769-5p plays a pivotal role in NSCLC by inhibiting cell proliferation, migration and invasion by targeting TGFBR1. |
format | Online Article Text |
id | pubmed-5768346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57683462018-01-25 miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma Yang, Zhao He, Jin Gao, Peng Niu, Yi Zhang, Jie Wang, Lei Liu, Meiyue Wei, Xiaomei Liu, Chunling Zhang, Chao Wang, Wei Du, Jiayi Li, Hongmin Hu, Wanning Sun, Guogui Oncotarget Research Paper MicroRNAs (miRNAs) are key regulators of multiple cancers, including non-small cell lung carcinoma (NSCLC). The aim of this study was to determine the expression pattern of miR-769-5p in NSCLC and to investigate its biological role during tumorigenesis. We showed that miR-769-5p was significantly downregulated and predicted poor prognosis in NSCLC compared with corresponding normal tissues. We then investigated its function and found that miR-769-5p significantly inhibited cell proliferation, migration and invasion in vitro and reduced tumor growth and metastasis in vivo. Furthermore, we explored the molecular mechanisms by which miR-769-5p contributes to NSCLC suppression and identified TGFBR1 as a direct target gene of miR-769-5p. Finally, we showed that TGFBR1 had opposite effects to those of miR-769-5p on lung cancer cells, suggesting that miR-769-5p might inhibit lung tumorigenesis by silencing TGFBR1. Taken together, our results demonstrated that miR-769-5p plays a pivotal role in NSCLC by inhibiting cell proliferation, migration and invasion by targeting TGFBR1. Impact Journals LLC 2017-12-08 /pmc/articles/PMC5768346/ /pubmed/29371929 http://dx.doi.org/10.18632/oncotarget.23060 Text en Copyright: © 2017 Yang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yang, Zhao He, Jin Gao, Peng Niu, Yi Zhang, Jie Wang, Lei Liu, Meiyue Wei, Xiaomei Liu, Chunling Zhang, Chao Wang, Wei Du, Jiayi Li, Hongmin Hu, Wanning Sun, Guogui miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma |
title | miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma |
title_full | miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma |
title_fullStr | miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma |
title_full_unstemmed | miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma |
title_short | miR-769-5p suppressed cell proliferation, migration and invasion by targeting TGFBR1 in non-small cell lung carcinoma |
title_sort | mir-769-5p suppressed cell proliferation, migration and invasion by targeting tgfbr1 in non-small cell lung carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768346/ https://www.ncbi.nlm.nih.gov/pubmed/29371929 http://dx.doi.org/10.18632/oncotarget.23060 |
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