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lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging

BACKGROUND: lncRNAs are widely involved in multiple malignancies including colorectal cancer (CRC). The expression and function of long intergenic non-protein coding RNA 460 (LINC00460) in CRC remains obscure. METHODS: In the present study, quantitative real-time PCR assays were applied to detect th...

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Autores principales: Zhang, Yueyan, Liu, Xingchi, Li, Qiang, Zhang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391123/
https://www.ncbi.nlm.nih.gov/pubmed/30863183
http://dx.doi.org/10.2147/CMAR.S192452
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author Zhang, Yueyan
Liu, Xingchi
Li, Qiang
Zhang, Yong
author_facet Zhang, Yueyan
Liu, Xingchi
Li, Qiang
Zhang, Yong
author_sort Zhang, Yueyan
collection PubMed
description BACKGROUND: lncRNAs are widely involved in multiple malignancies including colorectal cancer (CRC). The expression and function of long intergenic non-protein coding RNA 460 (LINC00460) in CRC remains obscure. METHODS: In the present study, quantitative real-time PCR assays were applied to detect the expression changes of LINC00460 and microRNA-939-5p (miR-939-5p) in CRC tissue specimens and cell lines. Western blot assays were used to measure the changes of LIMK2. Bioinformatics analysis, luciferase assays, and RNA pull-down assays were applied to determine the targeting binding effect between LINC00460 and miR-939-5p as well as LIMK2 and miR-939-5p. Transwell assays were used to evaluate the metastatic ability changes of CRC line HT29 and LOVO cells. RESULTS: We found that LINC00460 was upregulated and closely correlated to clinicopathological features and poor prognosis of patients with CRC. Functionally, we elucidated that LINC00460 promoted metastasis in CRC cell lines HT29 and LOVO. Further, we showed that LIMK2 was a downstream effector in the LINC00460-induced promotion of metastasis in CRC cells HT29 and LOVO. Through online bioinformatics analysis, LINC00460 and LIMK2 were demonstrated to share similar microRNA response elements for miR-939-5p. Then, LINC00460 and LIMK2 were verified to be the targets of miR-939-5p via a luciferase assay and an RNA pull-down assay. Also, miR-939-5p was showed to suppress metastasis by targeting of LIMK2. Lastly, we revealed that LINC00460 promoted LIMK2-mediated metastasis via miR-939-5p sponging in CRC cells HT29 and LOVO. CONCLUSION: The findings of this study showed that LINC00460 works as an oncogene in CRC and promoted CRC cell metastasis via regulation of miR-939-3p/LIMK2 axial. The present study might provide a new target in treating CRC.
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spelling pubmed-63911232019-03-12 lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging Zhang, Yueyan Liu, Xingchi Li, Qiang Zhang, Yong Cancer Manag Res Original Research BACKGROUND: lncRNAs are widely involved in multiple malignancies including colorectal cancer (CRC). The expression and function of long intergenic non-protein coding RNA 460 (LINC00460) in CRC remains obscure. METHODS: In the present study, quantitative real-time PCR assays were applied to detect the expression changes of LINC00460 and microRNA-939-5p (miR-939-5p) in CRC tissue specimens and cell lines. Western blot assays were used to measure the changes of LIMK2. Bioinformatics analysis, luciferase assays, and RNA pull-down assays were applied to determine the targeting binding effect between LINC00460 and miR-939-5p as well as LIMK2 and miR-939-5p. Transwell assays were used to evaluate the metastatic ability changes of CRC line HT29 and LOVO cells. RESULTS: We found that LINC00460 was upregulated and closely correlated to clinicopathological features and poor prognosis of patients with CRC. Functionally, we elucidated that LINC00460 promoted metastasis in CRC cell lines HT29 and LOVO. Further, we showed that LIMK2 was a downstream effector in the LINC00460-induced promotion of metastasis in CRC cells HT29 and LOVO. Through online bioinformatics analysis, LINC00460 and LIMK2 were demonstrated to share similar microRNA response elements for miR-939-5p. Then, LINC00460 and LIMK2 were verified to be the targets of miR-939-5p via a luciferase assay and an RNA pull-down assay. Also, miR-939-5p was showed to suppress metastasis by targeting of LIMK2. Lastly, we revealed that LINC00460 promoted LIMK2-mediated metastasis via miR-939-5p sponging in CRC cells HT29 and LOVO. CONCLUSION: The findings of this study showed that LINC00460 works as an oncogene in CRC and promoted CRC cell metastasis via regulation of miR-939-3p/LIMK2 axial. The present study might provide a new target in treating CRC. Dove Medical Press 2019-02-22 /pmc/articles/PMC6391123/ /pubmed/30863183 http://dx.doi.org/10.2147/CMAR.S192452 Text en © 2019 Zhang et al. 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.
spellingShingle Original Research
Zhang, Yueyan
Liu, Xingchi
Li, Qiang
Zhang, Yong
lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging
title lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging
title_full lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging
title_fullStr lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging
title_full_unstemmed lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging
title_short lncRNA LINC00460 promoted colorectal cancer cells metastasis via miR-939-5p sponging
title_sort lncrna linc00460 promoted colorectal cancer cells metastasis via mir-939-5p sponging
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391123/
https://www.ncbi.nlm.nih.gov/pubmed/30863183
http://dx.doi.org/10.2147/CMAR.S192452
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