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LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression

PURPOSE: The aim of this study was to study the roles and potential mechanism of LINC00520 in the progression of lung cancer. METHODS: The expression of LINC00520 and miR-3175 in lung cancer tissues and cells was detected by qRT-PCR. The relationship between LINC00520 level and disease stage was als...

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Autores principales: Xia, Gaowei, Li, Xiaoling, Chen, Fuhui, Shao, Zhenyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383105/
https://www.ncbi.nlm.nih.gov/pubmed/32801856
http://dx.doi.org/10.2147/CMAR.S250631
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author Xia, Gaowei
Li, Xiaoling
Chen, Fuhui
Shao, Zhenyu
author_facet Xia, Gaowei
Li, Xiaoling
Chen, Fuhui
Shao, Zhenyu
author_sort Xia, Gaowei
collection PubMed
description PURPOSE: The aim of this study was to study the roles and potential mechanism of LINC00520 in the progression of lung cancer. METHODS: The expression of LINC00520 and miR-3175 in lung cancer tissues and cells was detected by qRT-PCR. The relationship between LINC00520 level and disease stage was also calculated. Kaplan–Meier survival curve was drawn to observe the survival difference between high and low expression patients. Lipofectamine 2000 was used to transfect siLINC00520, miR-3175 inhibitor and their controls in lung cancer cells. CCK8 and colony formation assay were processed for cell proliferation. Transwell assay was undertaken for migration and invasion of lung cancer cells. MiRDB predicts the combination of LINC00520 and miR-3175. Luciferase and RNA pulldown assay were applied to verify the binding site. Correlation analysis of miR-3175 and LINC00520 expression in lung cancer tissues was shown. RESULTS: LINC00520 was highly expressed in lung cancer tissues and cells. Patients at III+IV stage were always with higher LINC00520 level than patients at I+II stage. Patients with high expression of lncRNA LINC00520 have short survival time (hazard ratio=1.7). Knockdown of LINC00520 inhibited proliferation, invasion and migration of lung cancer cells. LINC00520 targeted and negatively regulated miR-3175 (r=−0.528; P<0.001). MiR-3175 inhibitor rescued the effect of si-LINC00520 on lung cancer progression. CONCLUSION: LncRNA LINC00520 could predict poor prognosis and promote progression of lung cancer by inhibiting miR-3175 expression.
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spelling pubmed-73831052020-08-13 LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression Xia, Gaowei Li, Xiaoling Chen, Fuhui Shao, Zhenyu Cancer Manag Res Original Research PURPOSE: The aim of this study was to study the roles and potential mechanism of LINC00520 in the progression of lung cancer. METHODS: The expression of LINC00520 and miR-3175 in lung cancer tissues and cells was detected by qRT-PCR. The relationship between LINC00520 level and disease stage was also calculated. Kaplan–Meier survival curve was drawn to observe the survival difference between high and low expression patients. Lipofectamine 2000 was used to transfect siLINC00520, miR-3175 inhibitor and their controls in lung cancer cells. CCK8 and colony formation assay were processed for cell proliferation. Transwell assay was undertaken for migration and invasion of lung cancer cells. MiRDB predicts the combination of LINC00520 and miR-3175. Luciferase and RNA pulldown assay were applied to verify the binding site. Correlation analysis of miR-3175 and LINC00520 expression in lung cancer tissues was shown. RESULTS: LINC00520 was highly expressed in lung cancer tissues and cells. Patients at III+IV stage were always with higher LINC00520 level than patients at I+II stage. Patients with high expression of lncRNA LINC00520 have short survival time (hazard ratio=1.7). Knockdown of LINC00520 inhibited proliferation, invasion and migration of lung cancer cells. LINC00520 targeted and negatively regulated miR-3175 (r=−0.528; P<0.001). MiR-3175 inhibitor rescued the effect of si-LINC00520 on lung cancer progression. CONCLUSION: LncRNA LINC00520 could predict poor prognosis and promote progression of lung cancer by inhibiting miR-3175 expression. Dove 2020-07-17 /pmc/articles/PMC7383105/ /pubmed/32801856 http://dx.doi.org/10.2147/CMAR.S250631 Text en © 2020 Xia et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Xia, Gaowei
Li, Xiaoling
Chen, Fuhui
Shao, Zhenyu
LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression
title LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression
title_full LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression
title_fullStr LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression
title_full_unstemmed LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression
title_short LncRNA LINC00520 Predicts Poor Prognosis and Promotes Progression of Lung Cancer by Inhibiting MiR-3175 Expression
title_sort lncrna linc00520 predicts poor prognosis and promotes progression of lung cancer by inhibiting mir-3175 expression
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383105/
https://www.ncbi.nlm.nih.gov/pubmed/32801856
http://dx.doi.org/10.2147/CMAR.S250631
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