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EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis
Substantial evidence indicates that circular RNAs (circRNAs) play vital roles in several diseases, especially in cancer development. However, the functions of circRNAs in breast cancer metastasis remain to be investigated. This study aimed to identify the key circRNAs involved in epithelial mesenchy...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7169655/ https://www.ncbi.nlm.nih.gov/pubmed/32236616 http://dx.doi.org/10.3892/ijmm.2020.4550 |
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author | Yuan, Chunlei Luo, Xuliang Zhan, Xiang Zeng, Huihui Duan, Sijia |
author_facet | Yuan, Chunlei Luo, Xuliang Zhan, Xiang Zeng, Huihui Duan, Sijia |
author_sort | Yuan, Chunlei |
collection | PubMed |
description | Substantial evidence indicates that circular RNAs (circRNAs) play vital roles in several diseases, especially in cancer development. However, the functions of circRNAs in breast cancer metastasis remain to be investigated. This study aimed to identify the key circRNAs involved in epithelial mesenchymal transition (EMT) of breast cancer and evaluated their molecular function and roles in pathways that may be associated with tumor metastasis. An EMT model was constructed by treating breast cancer cells MCF-7 and MDA-MB-231 with transforming growth factor-β1. High-throughput RNA sequencing was used to identify the differentially expressed circRNAs in EMT and blank groups of two cells, and reverse transcription-quantitative PCR was used to validate the expression of circSCYL2 in human breast cancer tissues and cells. The effects of circSCYL2 on breast cancer cells were explored by transfecting with plasmids and the biological roles were assessed using transwell assays. EMT groups of breast cancer cells exhibited the characteristics of mesenchymal cells. Furthermore, the present study found that 7 circRNAs were significantly upregulated in both the MCF-7 EMT and MDA-MB-231 EMT groups, while 16 circRNAs were significantly downregulated. The current study identified that circSCYL2 was downregulated in breast cancer tissues and cell lines, and that circSCYL2 overexpression inhibited cell migration and invasion. This study provides expression profiles of circRNAs in EMT groups of breast cancer cells. circSCYL2, which is downregulated in breast cancer tissues and cells, may play an important role in breast cancer EMT progression. |
format | Online Article Text |
id | pubmed-7169655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-71696552020-04-24 EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis Yuan, Chunlei Luo, Xuliang Zhan, Xiang Zeng, Huihui Duan, Sijia Int J Mol Med Articles Substantial evidence indicates that circular RNAs (circRNAs) play vital roles in several diseases, especially in cancer development. However, the functions of circRNAs in breast cancer metastasis remain to be investigated. This study aimed to identify the key circRNAs involved in epithelial mesenchymal transition (EMT) of breast cancer and evaluated their molecular function and roles in pathways that may be associated with tumor metastasis. An EMT model was constructed by treating breast cancer cells MCF-7 and MDA-MB-231 with transforming growth factor-β1. High-throughput RNA sequencing was used to identify the differentially expressed circRNAs in EMT and blank groups of two cells, and reverse transcription-quantitative PCR was used to validate the expression of circSCYL2 in human breast cancer tissues and cells. The effects of circSCYL2 on breast cancer cells were explored by transfecting with plasmids and the biological roles were assessed using transwell assays. EMT groups of breast cancer cells exhibited the characteristics of mesenchymal cells. Furthermore, the present study found that 7 circRNAs were significantly upregulated in both the MCF-7 EMT and MDA-MB-231 EMT groups, while 16 circRNAs were significantly downregulated. The current study identified that circSCYL2 was downregulated in breast cancer tissues and cell lines, and that circSCYL2 overexpression inhibited cell migration and invasion. This study provides expression profiles of circRNAs in EMT groups of breast cancer cells. circSCYL2, which is downregulated in breast cancer tissues and cells, may play an important role in breast cancer EMT progression. D.A. Spandidos 2020-06 2020-03-24 /pmc/articles/PMC7169655/ /pubmed/32236616 http://dx.doi.org/10.3892/ijmm.2020.4550 Text en Copyright: © Yuan 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 Yuan, Chunlei Luo, Xuliang Zhan, Xiang Zeng, Huihui Duan, Sijia EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis |
title | EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis |
title_full | EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis |
title_fullStr | EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis |
title_full_unstemmed | EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis |
title_short | EMT related circular RNA expression profiles identify circSCYL2 as a novel molecule in breast tumor metastasis |
title_sort | emt related circular rna expression profiles identify circscyl2 as a novel molecule in breast tumor metastasis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7169655/ https://www.ncbi.nlm.nih.gov/pubmed/32236616 http://dx.doi.org/10.3892/ijmm.2020.4550 |
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