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MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells
BACKGROUND: MicroRNAs (miRNAs) have been reported to serve pivotal roles in tumorigenesis. This study sough to assess the expression and clinical significance of microRNA-1298 (miR-1298) in patients with non-small cell lung cancer (NSCLC), and explore the functional role of miR-1298 in tumorigenesis...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894281/ https://www.ncbi.nlm.nih.gov/pubmed/31801557 http://dx.doi.org/10.1186/s13000-019-0911-4 |
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author | Du, Zhonghai Wu, Jun Wang, Juan Liang, Yan Zhang, Sensen Shang, Zhimei Zuo, Wenchao |
author_facet | Du, Zhonghai Wu, Jun Wang, Juan Liang, Yan Zhang, Sensen Shang, Zhimei Zuo, Wenchao |
author_sort | Du, Zhonghai |
collection | PubMed |
description | BACKGROUND: MicroRNAs (miRNAs) have been reported to serve pivotal roles in tumorigenesis. This study sough to assess the expression and clinical significance of microRNA-1298 (miR-1298) in patients with non-small cell lung cancer (NSCLC), and explore the functional role of miR-1298 in tumorigenesis. METHODS: One hundred and twenty-one NSCLC patients were recruited in this study. The expression of miR-1298 was estimated using quantitative real-time PCR. Kaplan-Meier survival curves and Cox regression analysis were used to evaluate the prognostic value of miR-1298. Gain- and loss-of-function experiments were preformed to explore the biological function of miR-1298 in NSCLC cells. RESULTS: Expression levels of miR-1298 were downregulated in NSCLC tissues and cells compared with the corresponding normal controls. The decreased expression of miR-1298 was associated with patients’ lymph node metastasis and TNM stage. The low expression of miR-1298 predicted poor overall survival and served as an independent prognostic indicator in NSCLC patients. According to the cell experiments, NSCLC cell proliferation, migration and invasion were inhibited by the overexpression of miR-1298. CONCLUSION: All the data indicated that the downregulation of miR-1298 predicts poor prognosis of NSCLC, and the overexpression of miR-1298 in NSCLC cells leads to inhibited tumorigenesis. The aberrant miR-1298 may serve as a novel biomarker and therapeutic target in NSCLC. |
format | Online Article Text |
id | pubmed-6894281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68942812019-12-11 MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells Du, Zhonghai Wu, Jun Wang, Juan Liang, Yan Zhang, Sensen Shang, Zhimei Zuo, Wenchao Diagn Pathol Research BACKGROUND: MicroRNAs (miRNAs) have been reported to serve pivotal roles in tumorigenesis. This study sough to assess the expression and clinical significance of microRNA-1298 (miR-1298) in patients with non-small cell lung cancer (NSCLC), and explore the functional role of miR-1298 in tumorigenesis. METHODS: One hundred and twenty-one NSCLC patients were recruited in this study. The expression of miR-1298 was estimated using quantitative real-time PCR. Kaplan-Meier survival curves and Cox regression analysis were used to evaluate the prognostic value of miR-1298. Gain- and loss-of-function experiments were preformed to explore the biological function of miR-1298 in NSCLC cells. RESULTS: Expression levels of miR-1298 were downregulated in NSCLC tissues and cells compared with the corresponding normal controls. The decreased expression of miR-1298 was associated with patients’ lymph node metastasis and TNM stage. The low expression of miR-1298 predicted poor overall survival and served as an independent prognostic indicator in NSCLC patients. According to the cell experiments, NSCLC cell proliferation, migration and invasion were inhibited by the overexpression of miR-1298. CONCLUSION: All the data indicated that the downregulation of miR-1298 predicts poor prognosis of NSCLC, and the overexpression of miR-1298 in NSCLC cells leads to inhibited tumorigenesis. The aberrant miR-1298 may serve as a novel biomarker and therapeutic target in NSCLC. BioMed Central 2019-12-04 /pmc/articles/PMC6894281/ /pubmed/31801557 http://dx.doi.org/10.1186/s13000-019-0911-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Du, Zhonghai Wu, Jun Wang, Juan Liang, Yan Zhang, Sensen Shang, Zhimei Zuo, Wenchao MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells |
title | MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells |
title_full | MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells |
title_fullStr | MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells |
title_full_unstemmed | MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells |
title_short | MicroRNA-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells |
title_sort | microrna-1298 is downregulated in non-small cell lung cancer and suppresses tumor progression in tumor cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894281/ https://www.ncbi.nlm.nih.gov/pubmed/31801557 http://dx.doi.org/10.1186/s13000-019-0911-4 |
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