Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mei, Jie, Liu, Yan, Yu, Xinqian, Hao, Leiyu, Ma, Tao, Zhan, Qiang, Zhang, Yan, Zhu, Yichao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1783744681159426048
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
work_keys_str_mv AT meijie ywhazinteractswithdaam1topromotecellmigrationinbreastcancer
AT liuyan ywhazinteractswithdaam1topromotecellmigrationinbreastcancer
AT yuxinqian ywhazinteractswithdaam1topromotecellmigrationinbreastcancer
AT haoleiyu ywhazinteractswithdaam1topromotecellmigrationinbreastcancer
AT matao ywhazinteractswithdaam1topromotecellmigrationinbreastcancer
AT zhanqiang ywhazinteractswithdaam1topromotecellmigrationinbreastcancer
AT zhangyan ywhazinteractswithdaam1topromotecellmigrationinbreastcancer
AT zhuyichao ywhazinteractswithdaam1topromotecellmigrationinbreastcancer