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TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin

BACKGROUND: The urgent problem in the treatment of breast cancer is the recurrence induced by breast cancer stem cells (CSCs). Understanding the role and molecular mechanism of specific molecules in breast cancer stem cells can provide a theoretical basis for better treatment. TRIP6 is an adapter pr...

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Autores principales: Zhao, Xiaohui, Jiang, Chao, Xu, Rui, Liu, Qingnan, Liu, Guanglin, Zhang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023708/
https://www.ncbi.nlm.nih.gov/pubmed/32082081
http://dx.doi.org/10.1186/s12935-020-1136-z
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author Zhao, Xiaohui
Jiang, Chao
Xu, Rui
Liu, Qingnan
Liu, Guanglin
Zhang, Yan
author_facet Zhao, Xiaohui
Jiang, Chao
Xu, Rui
Liu, Qingnan
Liu, Guanglin
Zhang, Yan
author_sort Zhao, Xiaohui
collection PubMed
description BACKGROUND: The urgent problem in the treatment of breast cancer is the recurrence induced by breast cancer stem cells (CSCs). Understanding the role and molecular mechanism of specific molecules in breast cancer stem cells can provide a theoretical basis for better treatment. TRIP6 is an adapter protein which belongs to the zyxin family of LIM proteins and is important in regulating the functions of CSCs. The present study aims to investigate the effects and mechanism of TRIP6 in breast cancer. METHODS: TRIP6 expression in breast cancer cells and tissues were detected by Real-Time PCR, western blot and immunohistochemistry (IHC). MTT assays, colony formation assays, Xenografted tumor model and mammosphere formation assays were performed to investigate the oncogenic functions of TRIP6 in the tumorigenic capability and the tumor-initiating cell-like phenotype of breast cancer cells in vitro and in vivo. Luciferase reporter, subcellular fractionation and immunofluorescence staining assays were performed to determine the underlying mechanism of TRIP6-mediated stemness of breast cancer cells. RESULTS: TRIP6 expression was significantly upregulated in breast cancer, and was closely related to the clinicopathologic characteristics, poor overall survival (OS), relapse-free survival (RFS) and poor prognosis of breast cancer patients. Functional studies revealed that overexpression of TRIP6 significantly enhanced proliferative, tumorigenicity capability and the cancer stem cell-like properties of breast cancer in vitro and in vivo. On the contrary, silencing TRIP6 achieved the opposite results. Notably, we found that TRIP6 promoted Wnt/β-catenin signaling pathway in breast cancer to strengthen the tumor-initiating cell-like phenotype of breast cancer cells. CONCLUSIONS: This study indicates that TRIP6 plays an important role in maintaining the stem cell-like characteristics of breast cancer cells, supporting the significance of TRIP6 as a novel potential prognostic biomarker and therapeutic target for diagnosis and treatment of breast cancer.
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spelling pubmed-70237082020-02-20 TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin Zhao, Xiaohui Jiang, Chao Xu, Rui Liu, Qingnan Liu, Guanglin Zhang, Yan Cancer Cell Int Primary Research BACKGROUND: The urgent problem in the treatment of breast cancer is the recurrence induced by breast cancer stem cells (CSCs). Understanding the role and molecular mechanism of specific molecules in breast cancer stem cells can provide a theoretical basis for better treatment. TRIP6 is an adapter protein which belongs to the zyxin family of LIM proteins and is important in regulating the functions of CSCs. The present study aims to investigate the effects and mechanism of TRIP6 in breast cancer. METHODS: TRIP6 expression in breast cancer cells and tissues were detected by Real-Time PCR, western blot and immunohistochemistry (IHC). MTT assays, colony formation assays, Xenografted tumor model and mammosphere formation assays were performed to investigate the oncogenic functions of TRIP6 in the tumorigenic capability and the tumor-initiating cell-like phenotype of breast cancer cells in vitro and in vivo. Luciferase reporter, subcellular fractionation and immunofluorescence staining assays were performed to determine the underlying mechanism of TRIP6-mediated stemness of breast cancer cells. RESULTS: TRIP6 expression was significantly upregulated in breast cancer, and was closely related to the clinicopathologic characteristics, poor overall survival (OS), relapse-free survival (RFS) and poor prognosis of breast cancer patients. Functional studies revealed that overexpression of TRIP6 significantly enhanced proliferative, tumorigenicity capability and the cancer stem cell-like properties of breast cancer in vitro and in vivo. On the contrary, silencing TRIP6 achieved the opposite results. Notably, we found that TRIP6 promoted Wnt/β-catenin signaling pathway in breast cancer to strengthen the tumor-initiating cell-like phenotype of breast cancer cells. CONCLUSIONS: This study indicates that TRIP6 plays an important role in maintaining the stem cell-like characteristics of breast cancer cells, supporting the significance of TRIP6 as a novel potential prognostic biomarker and therapeutic target for diagnosis and treatment of breast cancer. BioMed Central 2020-02-14 /pmc/articles/PMC7023708/ /pubmed/32082081 http://dx.doi.org/10.1186/s12935-020-1136-z Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Primary Research
Zhao, Xiaohui
Jiang, Chao
Xu, Rui
Liu, Qingnan
Liu, Guanglin
Zhang, Yan
TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin
title TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin
title_full TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin
title_fullStr TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin
title_full_unstemmed TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin
title_short TRIP6 enhances stemness property of breast cancer cells through activation of Wnt/β-catenin
title_sort trip6 enhances stemness property of breast cancer cells through activation of wnt/β-catenin
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023708/
https://www.ncbi.nlm.nih.gov/pubmed/32082081
http://dx.doi.org/10.1186/s12935-020-1136-z
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