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Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer

In China, breast cancer is the most commonly occurring cancer in women. MicroRNAs (miRs) are a group of endogenous small non-coding RNAs, which serve a role in many biological processes through the regulation of target genes. In the current study, miR-150-5p expression was significantly up-regulated...

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Autores principales: Lu, Qingfu, Guo, Zhaoji, Qian, Haixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396020/
https://www.ncbi.nlm.nih.gov/pubmed/30867707
http://dx.doi.org/10.3892/etm.2019.7206
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author Lu, Qingfu
Guo, Zhaoji
Qian, Haixin
author_facet Lu, Qingfu
Guo, Zhaoji
Qian, Haixin
author_sort Lu, Qingfu
collection PubMed
description In China, breast cancer is the most commonly occurring cancer in women. MicroRNAs (miRs) are a group of endogenous small non-coding RNAs, which serve a role in many biological processes through the regulation of target genes. In the current study, miR-150-5p expression was significantly up-regulated in breast cancer tissues and cell lines. To investigate the cellular function and underlying molecular mechanism of miR-150-5p in breast cancer, TargetScan7.2 was used to identify miR-150-5p target genes. SRC kinase signaling inhibitor 1 (SRCIN1) was identified as a direct target gene of miR-150-5p and the current study demonstrated that SRCIN1 was negatively regulated by miR-150-5p in breast cancer cells. Furthermore, SRCIN1 expression was significantly down-regulated in breast cancer tissues and cell lines. Taken together, these results demonstrated that there was a negative association between miR-150-5p and SRCIN1 in breast cancer. The CCK-8 and Transwell assays were used to examine breast cancer cell viability, invasion and migration ability. The current study demonstrated that over-expression of miR-150-5p enhanced breast cancer cell proliferation, invasion and migration. In addition, miR-150-5p over-expression increased the expression of mesenchymal cell markers (vimentin, N-cadherin and β-catenin) and decreased the expression of epithelial cell markers (E-cadherin and zonula occludens-1). By contrast, miR-150-5p knockdown inhibited breast cancer cell viability, invasion and migration. Additionally, miR-150-5p knockdown decreased the expression of mesenchymal cell markers and increased the expression of epithelial cell markers. Taken together, these results suggest that the miR-150-5p/SRCIN1 axis may be a potential target in the treatment of breast cancer.
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spelling pubmed-63960202019-03-13 Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer Lu, Qingfu Guo, Zhaoji Qian, Haixin Exp Ther Med Articles In China, breast cancer is the most commonly occurring cancer in women. MicroRNAs (miRs) are a group of endogenous small non-coding RNAs, which serve a role in many biological processes through the regulation of target genes. In the current study, miR-150-5p expression was significantly up-regulated in breast cancer tissues and cell lines. To investigate the cellular function and underlying molecular mechanism of miR-150-5p in breast cancer, TargetScan7.2 was used to identify miR-150-5p target genes. SRC kinase signaling inhibitor 1 (SRCIN1) was identified as a direct target gene of miR-150-5p and the current study demonstrated that SRCIN1 was negatively regulated by miR-150-5p in breast cancer cells. Furthermore, SRCIN1 expression was significantly down-regulated in breast cancer tissues and cell lines. Taken together, these results demonstrated that there was a negative association between miR-150-5p and SRCIN1 in breast cancer. The CCK-8 and Transwell assays were used to examine breast cancer cell viability, invasion and migration ability. The current study demonstrated that over-expression of miR-150-5p enhanced breast cancer cell proliferation, invasion and migration. In addition, miR-150-5p over-expression increased the expression of mesenchymal cell markers (vimentin, N-cadherin and β-catenin) and decreased the expression of epithelial cell markers (E-cadherin and zonula occludens-1). By contrast, miR-150-5p knockdown inhibited breast cancer cell viability, invasion and migration. Additionally, miR-150-5p knockdown decreased the expression of mesenchymal cell markers and increased the expression of epithelial cell markers. Taken together, these results suggest that the miR-150-5p/SRCIN1 axis may be a potential target in the treatment of breast cancer. D.A. Spandidos 2019-03 2019-01-28 /pmc/articles/PMC6396020/ /pubmed/30867707 http://dx.doi.org/10.3892/etm.2019.7206 Text en Copyright: © Lu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Lu, Qingfu
Guo, Zhaoji
Qian, Haixin
Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer
title Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer
title_full Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer
title_fullStr Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer
title_full_unstemmed Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer
title_short Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer
title_sort role of microrna-150-5p/srcin1 axis in the progression of breast cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396020/
https://www.ncbi.nlm.nih.gov/pubmed/30867707
http://dx.doi.org/10.3892/etm.2019.7206
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