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LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis

Breast cancer is the most common malignant tumor among women worldwide. Although increasing evidence indicates that long noncoding RNAs (lncRNAs) play critical roles during breast tumorigenesis and progression, the involvement of most lncRNAs in breast cancer remains largely unknown. In the current...

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Autores principales: Ji, Wei, Diao, Yu-Ling, Qiu, Yi-Ran, Ge, Jie, Cao, Xu-Chen, Yu, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944690/
https://www.ncbi.nlm.nih.gov/pubmed/31907362
http://dx.doi.org/10.1038/s41419-019-2213-x
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author Ji, Wei
Diao, Yu-Ling
Qiu, Yi-Ran
Ge, Jie
Cao, Xu-Chen
Yu, Yue
author_facet Ji, Wei
Diao, Yu-Ling
Qiu, Yi-Ran
Ge, Jie
Cao, Xu-Chen
Yu, Yue
author_sort Ji, Wei
collection PubMed
description Breast cancer is the most common malignant tumor among women worldwide. Although increasing evidence indicates that long noncoding RNAs (lncRNAs) play critical roles during breast tumorigenesis and progression, the involvement of most lncRNAs in breast cancer remains largely unknown. In the current study, we demonstrated that LINC00665 promotes breast cancer cell proliferation, migration, and invasion. Accumulating evidence indicates that many lncRNAs can function as endogenous miRNA sponges by competitively binding common miRNAs. In this study, we demonstrated that LINC00665 functions as a sponge for miR-379-5p, reducing the ability of miR-379-5p to repress LIN28B. LINC00665 promoted breast cancer progression and induced an epithelial–mesenchymal transition-like phenotype via the upregulation of LIN28B expression. Clinically, LINC00665 expression was increased but miR-379-5p expression was decreased in breast cancer tissues compared with that in normal breast tissues in the TCGA database. Furthermore, the expression of LINC00665 was negatively related with miR-379-5p expression. Collectively, our results reveal the LINC00665–miR-379-5p–LIN28B axis and shed light on breast cancer therapy.
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spelling pubmed-69446902020-01-07 LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis Ji, Wei Diao, Yu-Ling Qiu, Yi-Ran Ge, Jie Cao, Xu-Chen Yu, Yue Cell Death Dis Article Breast cancer is the most common malignant tumor among women worldwide. Although increasing evidence indicates that long noncoding RNAs (lncRNAs) play critical roles during breast tumorigenesis and progression, the involvement of most lncRNAs in breast cancer remains largely unknown. In the current study, we demonstrated that LINC00665 promotes breast cancer cell proliferation, migration, and invasion. Accumulating evidence indicates that many lncRNAs can function as endogenous miRNA sponges by competitively binding common miRNAs. In this study, we demonstrated that LINC00665 functions as a sponge for miR-379-5p, reducing the ability of miR-379-5p to repress LIN28B. LINC00665 promoted breast cancer progression and induced an epithelial–mesenchymal transition-like phenotype via the upregulation of LIN28B expression. Clinically, LINC00665 expression was increased but miR-379-5p expression was decreased in breast cancer tissues compared with that in normal breast tissues in the TCGA database. Furthermore, the expression of LINC00665 was negatively related with miR-379-5p expression. Collectively, our results reveal the LINC00665–miR-379-5p–LIN28B axis and shed light on breast cancer therapy. Nature Publishing Group UK 2020-01-06 /pmc/articles/PMC6944690/ /pubmed/31907362 http://dx.doi.org/10.1038/s41419-019-2213-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ji, Wei
Diao, Yu-Ling
Qiu, Yi-Ran
Ge, Jie
Cao, Xu-Chen
Yu, Yue
LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis
title LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis
title_full LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis
title_fullStr LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis
title_full_unstemmed LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis
title_short LINC00665 promotes breast cancer progression through regulation of the miR-379-5p/LIN28B axis
title_sort linc00665 promotes breast cancer progression through regulation of the mir-379-5p/lin28b axis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944690/
https://www.ncbi.nlm.nih.gov/pubmed/31907362
http://dx.doi.org/10.1038/s41419-019-2213-x
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