IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v10y2019i1d10.1038_s41467-019-13700-6.html
   My bibliography  Save this article

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

Author

Listed:
  • Jin-mei Yu

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Wei Sun

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Zhen-he Wang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Xiao Liang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Fang Hua

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Ke Li

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Xiao-xi Lv

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Xiao-wei Zhang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Yu-ying Liu

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Jiao-jiao Yu

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Shan-shan Liu

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Shuang Shang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Feng Wang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Zhao-na Yang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Chen-xi Zhao

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Xue-ying Hou

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Ping-ping Li

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Bo Huang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Bing Cui

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Zhuo-Wei Hu

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

Abstract

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.

Suggested Citation

  • Jin-mei Yu & Wei Sun & Zhen-he Wang & Xiao Liang & Fang Hua & Ke Li & Xiao-xi Lv & Xiao-wei Zhang & Yu-ying Liu & Jiao-jiao Yu & Shan-shan Liu & Shuang Shang & Feng Wang & Zhao-na Yang & Chen-xi Zhao , 2019. "TRIB3 supports breast cancer stemness by suppressing FOXO1 degradation and enhancing SOX2 transcription," Nature Communications, Nature, vol. 10(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-13700-6
    DOI: 10.1038/s41467-019-13700-6
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-019-13700-6
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-019-13700-6?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-13700-6. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.