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Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7

Breast cancer is the second leading cause of cancer‐related deaths in women. The long noncoding RNA LINC00115 has been reported to be involved in the poor outcome of patients with breast cancer, but the biological function and underlying mechanism remain unclear. Here, we report that LINC00115 expre...

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Detalles Bibliográficos
Autores principales: Yuan, Chunlei, Luo, Xuliang, Duan, Sijia, Guo, Liangyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327907/
https://www.ncbi.nlm.nih.gov/pubmed/32175684
http://dx.doi.org/10.1002/2211-5463.12842
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author Yuan, Chunlei
Luo, Xuliang
Duan, Sijia
Guo, Liangyun
author_facet Yuan, Chunlei
Luo, Xuliang
Duan, Sijia
Guo, Liangyun
author_sort Yuan, Chunlei
collection PubMed
description Breast cancer is the second leading cause of cancer‐related deaths in women. The long noncoding RNA LINC00115 has been reported to be involved in the poor outcome of patients with breast cancer, but the biological function and underlying mechanism remain unclear. Here, we report that LINC00115 expression is increased in triple‐negative breast cancer tissue compared with matched normal tissue, and LINC00115 knockdown suppresses breast cancer cell migration and invasion. Furthermore, we show that LINC00115 directly targets miR‐7 and inhibits its expression. LINC00115 also reduces the expression of KLF4, which is a direct target of miR‐7 and is involved in breast cancer metastasis. Together, our findings suggest that LINC00115 promotes breast cancer metastasis through modulating the expression of miR‐7 and KLF4.
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spelling pubmed-73279072020-07-02 Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7 Yuan, Chunlei Luo, Xuliang Duan, Sijia Guo, Liangyun FEBS Open Bio Research Articles Breast cancer is the second leading cause of cancer‐related deaths in women. The long noncoding RNA LINC00115 has been reported to be involved in the poor outcome of patients with breast cancer, but the biological function and underlying mechanism remain unclear. Here, we report that LINC00115 expression is increased in triple‐negative breast cancer tissue compared with matched normal tissue, and LINC00115 knockdown suppresses breast cancer cell migration and invasion. Furthermore, we show that LINC00115 directly targets miR‐7 and inhibits its expression. LINC00115 also reduces the expression of KLF4, which is a direct target of miR‐7 and is involved in breast cancer metastasis. Together, our findings suggest that LINC00115 promotes breast cancer metastasis through modulating the expression of miR‐7 and KLF4. John Wiley and Sons Inc. 2020-06-11 /pmc/articles/PMC7327907/ /pubmed/32175684 http://dx.doi.org/10.1002/2211-5463.12842 Text en © 2020 The Second Affiliated Hospital of Nanchang University. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Yuan, Chunlei
Luo, Xuliang
Duan, Sijia
Guo, Liangyun
Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7
title Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7
title_full Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7
title_fullStr Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7
title_full_unstemmed Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7
title_short Long noncoding RNA LINC00115 promotes breast cancer metastasis by inhibiting miR‐7
title_sort long noncoding rna linc00115 promotes breast cancer metastasis by inhibiting mir‐7
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327907/
https://www.ncbi.nlm.nih.gov/pubmed/32175684
http://dx.doi.org/10.1002/2211-5463.12842
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