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LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p

BACKGROUND: This study mainly explored the expression level of LINC-PINT in bladder cancer and its relationship with prognosis. Meanwhile, the effect of LINC-PINT on the biological function of bladder cancer was also explored. METHODS: The expression levels of LINC-PINT and miR-155-5p were detected...

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Autores principales: Han, Xiancheng, Liu, Jing, Liu, Yongguo, Mou, Linkai, Li, Chunlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179740/
https://www.ncbi.nlm.nih.gov/pubmed/34103994
http://dx.doi.org/10.2147/CMAR.S305547
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author Han, Xiancheng
Liu, Jing
Liu, Yongguo
Mou, Linkai
Li, Chunlong
author_facet Han, Xiancheng
Liu, Jing
Liu, Yongguo
Mou, Linkai
Li, Chunlong
author_sort Han, Xiancheng
collection PubMed
description BACKGROUND: This study mainly explored the expression level of LINC-PINT in bladder cancer and its relationship with prognosis. Meanwhile, the effect of LINC-PINT on the biological function of bladder cancer was also explored. METHODS: The expression levels of LINC-PINT and miR-155-5p were detected by qRT-PCR. The prognostic significance of LINC-PINT in bladder cancer was studied by the Kaplan–Meier curve and Log rank test. CCK-8 and Transwell assays were used to analyze the proliferation, migration, and invasion ability. The targeting relationship between LINC-PINT and miR-155-5p was analyzed using bioinformatics and dual-luciferase reporter assays. RESULTS: The expression of LINC-PINT was downregulated in bladder cancer tissues and cell lines, and miR-155-5p showed the opposite trend in bladder cancer tissues. Kaplan–Meier curve proved that the patients with low LINC-PINT expression had a lower five-year survival rate and the Log rank test displayed that LINC-PINT was a prognostic factor of BC. CCK-8 and Transwell results showed that LINC-PINT could inhibit the ability of proliferation, migration, and invasion. LINC-PINT was proved to target miR-155-5p in bladder cancer. Dual-luciferase reporter gene assay showed that the relative luciferase activity of overexpression miR-155-5p co-transfected with LINC-PINT-wt was significantly lower. LINC-PINT was negatively correlated with miR-155-5p. CONCLUSION: LINC-PINT is a potential prognostic marker of bladder cancer, and the up-regulation of Lin-PINT can inhibit the proliferation, invasion, and migration of bladder cancer cells by targeting miR-155-5p.
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spelling pubmed-81797402021-06-07 LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p Han, Xiancheng Liu, Jing Liu, Yongguo Mou, Linkai Li, Chunlong Cancer Manag Res Original Research BACKGROUND: This study mainly explored the expression level of LINC-PINT in bladder cancer and its relationship with prognosis. Meanwhile, the effect of LINC-PINT on the biological function of bladder cancer was also explored. METHODS: The expression levels of LINC-PINT and miR-155-5p were detected by qRT-PCR. The prognostic significance of LINC-PINT in bladder cancer was studied by the Kaplan–Meier curve and Log rank test. CCK-8 and Transwell assays were used to analyze the proliferation, migration, and invasion ability. The targeting relationship between LINC-PINT and miR-155-5p was analyzed using bioinformatics and dual-luciferase reporter assays. RESULTS: The expression of LINC-PINT was downregulated in bladder cancer tissues and cell lines, and miR-155-5p showed the opposite trend in bladder cancer tissues. Kaplan–Meier curve proved that the patients with low LINC-PINT expression had a lower five-year survival rate and the Log rank test displayed that LINC-PINT was a prognostic factor of BC. CCK-8 and Transwell results showed that LINC-PINT could inhibit the ability of proliferation, migration, and invasion. LINC-PINT was proved to target miR-155-5p in bladder cancer. Dual-luciferase reporter gene assay showed that the relative luciferase activity of overexpression miR-155-5p co-transfected with LINC-PINT-wt was significantly lower. LINC-PINT was negatively correlated with miR-155-5p. CONCLUSION: LINC-PINT is a potential prognostic marker of bladder cancer, and the up-regulation of Lin-PINT can inhibit the proliferation, invasion, and migration of bladder cancer cells by targeting miR-155-5p. Dove 2021-06-01 /pmc/articles/PMC8179740/ /pubmed/34103994 http://dx.doi.org/10.2147/CMAR.S305547 Text en © 2021 Han et al. https://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/ (https://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
Han, Xiancheng
Liu, Jing
Liu, Yongguo
Mou, Linkai
Li, Chunlong
LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p
title LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p
title_full LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p
title_fullStr LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p
title_full_unstemmed LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p
title_short LINC-PINT Inhibited Malignant Progression of Bladder Cancer by Targeting miR-155-5p
title_sort linc-pint inhibited malignant progression of bladder cancer by targeting mir-155-5p
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179740/
https://www.ncbi.nlm.nih.gov/pubmed/34103994
http://dx.doi.org/10.2147/CMAR.S305547
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