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Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ
BACKGROUND: Breast cancer is a most common type of cancer in women. Circular RNAs (circRNAs) are involved in cancer development and progression, but their roles and regulatory mechanisms are unclear in breast cancer. Our previous study indicated that has_circ_0001667 (circ_0001667) was up-regulated...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937801/ https://www.ncbi.nlm.nih.gov/pubmed/31893023 http://dx.doi.org/10.1186/s13578-019-0359-y |
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author | Geng, Zhongli Wang, Wei Chen, Hui Mao, Jianya Li, Zhenguo Zhou, Jing |
author_facet | Geng, Zhongli Wang, Wei Chen, Hui Mao, Jianya Li, Zhenguo Zhou, Jing |
author_sort | Geng, Zhongli |
collection | PubMed |
description | BACKGROUND: Breast cancer is a most common type of cancer in women. Circular RNAs (circRNAs) are involved in cancer development and progression, but their roles and regulatory mechanisms are unclear in breast cancer. Our previous study indicated that has_circ_0001667 (circ_0001667) was up-regulated in breast cancer from the array and might play an oncogenic role, however, the roles of circ_0001667 were not known. This study was aimed to investigate the role and the underlying molecular mechanism of circ_0001667 in breast cancer. RESULTS: The real-time PCR result showed that circ_0001667 was overexpressed in breast cancer tissues or cell lines compared to the adjacent normal tissues or normal cells. There was a negative relationship between circ_0001667 levels and the life time of breast cancer patients. Meanwhile, the inhibition of circ_0001667 suppressed the proliferation and metastasis of human breast cancer cells. Further bioinformatical analysis indicated that circ_0001667 sponged miR-125a-5p to regulate TAZ expression by Targetscan and miRanda. Dual luciferase reporter assay and western blotting experiments revealed that circ_0001667 negatively regulated miR-125a-5p expression leading to promoting TAZ expression through Hippo signal pathway in breast cancer cells. CONCLUSIONS: This study uncovered that circ_0001667 was a potential breast cancer prognostic marker, as well as a potential therapeutic target to inhibit breast cancer metastasis by circ_0001667/miR-125a-5p/TAZ axis. |
format | Online Article Text |
id | pubmed-6937801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69378012019-12-31 Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ Geng, Zhongli Wang, Wei Chen, Hui Mao, Jianya Li, Zhenguo Zhou, Jing Cell Biosci Research BACKGROUND: Breast cancer is a most common type of cancer in women. Circular RNAs (circRNAs) are involved in cancer development and progression, but their roles and regulatory mechanisms are unclear in breast cancer. Our previous study indicated that has_circ_0001667 (circ_0001667) was up-regulated in breast cancer from the array and might play an oncogenic role, however, the roles of circ_0001667 were not known. This study was aimed to investigate the role and the underlying molecular mechanism of circ_0001667 in breast cancer. RESULTS: The real-time PCR result showed that circ_0001667 was overexpressed in breast cancer tissues or cell lines compared to the adjacent normal tissues or normal cells. There was a negative relationship between circ_0001667 levels and the life time of breast cancer patients. Meanwhile, the inhibition of circ_0001667 suppressed the proliferation and metastasis of human breast cancer cells. Further bioinformatical analysis indicated that circ_0001667 sponged miR-125a-5p to regulate TAZ expression by Targetscan and miRanda. Dual luciferase reporter assay and western blotting experiments revealed that circ_0001667 negatively regulated miR-125a-5p expression leading to promoting TAZ expression through Hippo signal pathway in breast cancer cells. CONCLUSIONS: This study uncovered that circ_0001667 was a potential breast cancer prognostic marker, as well as a potential therapeutic target to inhibit breast cancer metastasis by circ_0001667/miR-125a-5p/TAZ axis. BioMed Central 2019-12-30 /pmc/articles/PMC6937801/ /pubmed/31893023 http://dx.doi.org/10.1186/s13578-019-0359-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Geng, Zhongli Wang, Wei Chen, Hui Mao, Jianya Li, Zhenguo Zhou, Jing Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ |
title | Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ |
title_full | Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ |
title_fullStr | Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ |
title_full_unstemmed | Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ |
title_short | Circ_0001667 promotes breast cancer cell proliferation and survival via Hippo signal pathway by regulating TAZ |
title_sort | circ_0001667 promotes breast cancer cell proliferation and survival via hippo signal pathway by regulating taz |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937801/ https://www.ncbi.nlm.nih.gov/pubmed/31893023 http://dx.doi.org/10.1186/s13578-019-0359-y |
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