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YWHAZ interacts with DAAM1 to promote cell migration in breast cancer
Dishevelled-associated activator of morphogenesis 1 (DAAM1) is a critical driver in facilitating metastasis in breast cancer (BrCa). However, molecular mechanisms for the regulation of DAAM1 activation are only partially elucidated. In this research, the expression levels of YWHAZ and DAAM1 were exa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397740/ https://www.ncbi.nlm.nih.gov/pubmed/34453038 http://dx.doi.org/10.1038/s41420-021-00609-7 |
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author | Mei, Jie Liu, Yan Yu, Xinqian Hao, Leiyu Ma, Tao Zhan, Qiang Zhang, Yan Zhu, Yichao |
author_facet | Mei, Jie Liu, Yan Yu, Xinqian Hao, Leiyu Ma, Tao Zhan, Qiang Zhang, Yan Zhu, Yichao |
author_sort | Mei, Jie |
collection | PubMed |
description | Dishevelled-associated activator of morphogenesis 1 (DAAM1) is a critical driver in facilitating metastasis in breast cancer (BrCa). However, molecular mechanisms for the regulation of DAAM1 activation are only partially elucidated. In this research, the expression levels of YWHAZ and DAAM1 were examined by immunohistochemistry (IHC) staining in BrCa tissues. The functional roles of tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta (YWHAZ)–DAAM1 axis and their regulator microRNA-613 (miR-613) in BrCa cells and associated molecular mechanisms were demonstrated in vitro. As results, the expression levels of DAAM1 and YWHAZ were significantly upregulated in BrCa tissues compared with normal tissues and remarkably associated with poor prognosis. Besides, DAAM1 and YWHAZ were positively correlated with each other in BrCa tissues. YWHAZ interacted and colocalized with DAAM1 in BrCa cells, which was essential for DAAM1-mediated microfilament remodeling and RhoA activation. Moreover, miR-613 directly targeted both YWHAZ and DAAM1, contributing to inhibiting BrCa cells migration via blocking the complex of YWHAZ–DAAM1. To sum up, these data reveal that YWHAZ regulates DAAM1 activation, and the YWHAZ–DAAM1 complex is directly targeted by the shared post-transcriptional regulator miR-613. |
format | Online Article Text |
id | pubmed-8397740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83977402021-09-15 YWHAZ interacts with DAAM1 to promote cell migration in breast cancer Mei, Jie Liu, Yan Yu, Xinqian Hao, Leiyu Ma, Tao Zhan, Qiang Zhang, Yan Zhu, Yichao Cell Death Discov Article Dishevelled-associated activator of morphogenesis 1 (DAAM1) is a critical driver in facilitating metastasis in breast cancer (BrCa). However, molecular mechanisms for the regulation of DAAM1 activation are only partially elucidated. In this research, the expression levels of YWHAZ and DAAM1 were examined by immunohistochemistry (IHC) staining in BrCa tissues. The functional roles of tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta (YWHAZ)–DAAM1 axis and their regulator microRNA-613 (miR-613) in BrCa cells and associated molecular mechanisms were demonstrated in vitro. As results, the expression levels of DAAM1 and YWHAZ were significantly upregulated in BrCa tissues compared with normal tissues and remarkably associated with poor prognosis. Besides, DAAM1 and YWHAZ were positively correlated with each other in BrCa tissues. YWHAZ interacted and colocalized with DAAM1 in BrCa cells, which was essential for DAAM1-mediated microfilament remodeling and RhoA activation. Moreover, miR-613 directly targeted both YWHAZ and DAAM1, contributing to inhibiting BrCa cells migration via blocking the complex of YWHAZ–DAAM1. To sum up, these data reveal that YWHAZ regulates DAAM1 activation, and the YWHAZ–DAAM1 complex is directly targeted by the shared post-transcriptional regulator miR-613. Nature Publishing Group UK 2021-08-27 /pmc/articles/PMC8397740/ /pubmed/34453038 http://dx.doi.org/10.1038/s41420-021-00609-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mei, Jie Liu, Yan Yu, Xinqian Hao, Leiyu Ma, Tao Zhan, Qiang Zhang, Yan Zhu, Yichao YWHAZ interacts with DAAM1 to promote cell migration in breast cancer |
title | YWHAZ interacts with DAAM1 to promote cell migration in breast cancer |
title_full | YWHAZ interacts with DAAM1 to promote cell migration in breast cancer |
title_fullStr | YWHAZ interacts with DAAM1 to promote cell migration in breast cancer |
title_full_unstemmed | YWHAZ interacts with DAAM1 to promote cell migration in breast cancer |
title_short | YWHAZ interacts with DAAM1 to promote cell migration in breast cancer |
title_sort | ywhaz interacts with daam1 to promote cell migration in breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397740/ https://www.ncbi.nlm.nih.gov/pubmed/34453038 http://dx.doi.org/10.1038/s41420-021-00609-7 |
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