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TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription

The existence of breast cancer stem cells (BCSCs) is a major reason underlying cancer metastasis and recurrence after chemotherapy and radiotherapy. Targeting BCSCs may ameliorate breast cancer relapse and therapy resistance. Here we report that expression of the pseudokinase Tribble 3 (TRIB3) posit...

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Autores principales: Yu, Jin-mei, Sun, Wei, Wang, Zhen-he, Liang, Xiao, Hua, Fang, Li, Ke, Lv, Xiao-xi, Zhang, Xiao-wei, Liu, Yu-ying, Yu, Jiao-jiao, Liu, Shan-shan, Shang, Shuang, Wang, Feng, Yang, Zhao-na, Zhao, Chen-xi, Hou, Xue-ying, Li, Ping-ping, Huang, Bo, Cui, Bing, Hu, Zhuo-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915745/
https://www.ncbi.nlm.nih.gov/pubmed/31844113
http://dx.doi.org/10.1038/s41467-019-13700-6
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author Yu, Jin-mei
Sun, Wei
Wang, Zhen-he
Liang, Xiao
Hua, Fang
Li, Ke
Lv, Xiao-xi
Zhang, Xiao-wei
Liu, Yu-ying
Yu, Jiao-jiao
Liu, Shan-shan
Shang, Shuang
Wang, Feng
Yang, Zhao-na
Zhao, Chen-xi
Hou, Xue-ying
Li, Ping-ping
Huang, Bo
Cui, Bing
Hu, Zhuo-Wei
author_facet Yu, Jin-mei
Sun, Wei
Wang, Zhen-he
Liang, Xiao
Hua, Fang
Li, Ke
Lv, Xiao-xi
Zhang, Xiao-wei
Liu, Yu-ying
Yu, Jiao-jiao
Liu, Shan-shan
Shang, Shuang
Wang, Feng
Yang, Zhao-na
Zhao, Chen-xi
Hou, Xue-ying
Li, Ping-ping
Huang, Bo
Cui, Bing
Hu, Zhuo-Wei
author_sort Yu, Jin-mei
collection PubMed
description The existence of breast cancer stem cells (BCSCs) is a major reason underlying cancer metastasis and recurrence after chemotherapy and radiotherapy. Targeting BCSCs may ameliorate breast cancer relapse and therapy resistance. Here we report that expression of the pseudokinase Tribble 3 (TRIB3) positively associates with breast cancer stemness and progression. Elevated TRIB3 expression supports BCSCs by interacting with AKT to interfere with the FOXO1-AKT interaction and suppress FOXO1 phosphorylation, ubiquitination, and degradation by E3 ligases SKP2 and NEDD4L. The accumulated FOXO1 promotes transcriptional expression of SOX2, a transcriptional factor for cancer stemness, which in turn, activates FOXO1 transcription and forms a positive regulatory loop. Disturbing the TRIB3-AKT interaction suppresses BCSCs by accelerating FOXO1 degradation and reducing SOX2 expression in mouse models of breast cancer. Our study provides insights into breast cancer development and confers a potential therapeutic strategy against TRIB3-overexpressed breast cancer.
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spelling pubmed-69157452019-12-18 TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription Yu, Jin-mei Sun, Wei Wang, Zhen-he Liang, Xiao Hua, Fang Li, Ke Lv, Xiao-xi Zhang, Xiao-wei Liu, Yu-ying Yu, Jiao-jiao Liu, Shan-shan Shang, Shuang Wang, Feng Yang, Zhao-na Zhao, Chen-xi Hou, Xue-ying Li, Ping-ping Huang, Bo Cui, Bing Hu, Zhuo-Wei Nat Commun Article The existence of breast cancer stem cells (BCSCs) is a major reason underlying cancer metastasis and recurrence after chemotherapy and radiotherapy. Targeting BCSCs may ameliorate breast cancer relapse and therapy resistance. Here we report that expression of the pseudokinase Tribble 3 (TRIB3) positively associates with breast cancer stemness and progression. Elevated TRIB3 expression supports BCSCs by interacting with AKT to interfere with the FOXO1-AKT interaction and suppress FOXO1 phosphorylation, ubiquitination, and degradation by E3 ligases SKP2 and NEDD4L. The accumulated FOXO1 promotes transcriptional expression of SOX2, a transcriptional factor for cancer stemness, which in turn, activates FOXO1 transcription and forms a positive regulatory loop. Disturbing the TRIB3-AKT interaction suppresses BCSCs by accelerating FOXO1 degradation and reducing SOX2 expression in mouse models of breast cancer. Our study provides insights into breast cancer development and confers a potential therapeutic strategy against TRIB3-overexpressed breast cancer. Nature Publishing Group UK 2019-12-16 /pmc/articles/PMC6915745/ /pubmed/31844113 http://dx.doi.org/10.1038/s41467-019-13700-6 Text en © The Author(s) 2019 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/.
spellingShingle Article
Yu, Jin-mei
Sun, Wei
Wang, Zhen-he
Liang, Xiao
Hua, Fang
Li, Ke
Lv, Xiao-xi
Zhang, Xiao-wei
Liu, Yu-ying
Yu, Jiao-jiao
Liu, Shan-shan
Shang, Shuang
Wang, Feng
Yang, Zhao-na
Zhao, Chen-xi
Hou, Xue-ying
Li, Ping-ping
Huang, Bo
Cui, Bing
Hu, Zhuo-Wei
TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription
title TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription
title_full TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription
title_fullStr TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription
title_full_unstemmed TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription
title_short TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription
title_sort trib3 supports breast cancer stemness by suppressing foxo1 degradation and enhancing sox2 transcription
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915745/
https://www.ncbi.nlm.nih.gov/pubmed/31844113
http://dx.doi.org/10.1038/s41467-019-13700-6
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