中文版 | English
Title

FOXA1 O-GlcNAcylation-mediated transcriptional switch governs metastasis capacity in breast cancer

Author
Corresponding AuthorWu, Sijin; Zhang, Jianing; Liu, Yubo
Publication Years
2023-08-01
DOI
Source Title
ISSN
2375-2548
Volume9Issue:33
Abstract
FOXA1, a transcription factor involved in epigenetic reprogramming, is crucial for breast cancer progression. However, the mechanisms by which FOXA1 achieves its oncogenic functions remain elusive. Here, we demonstrate that the O-linked beta-N-acetylglucosamine modification (O-GlcNAcylation) of FOXA1 promotes breast cancer metastasis by orchestrating the transcription of numerous metastasis regulators. O-GlcNAcylation at Thr(432), Ser(441), and Ser(443) regulates the stability of FOXA1 and promotes its assembly with chromatin. O-GlcNAcylation shapes the FOXA1 interactome, especially triggering the recruitment of the transcriptional repressor methyl-CpG binding protein 2 and consequently stimulating FOXA1 chromatin-binding sites to switch to chromatin loci of adhesion-related genes, including EPB41L3 and COL9A2. Site-specific depletion of O-GlcNAcylation on FOXA1 affects the expression of various downstream genes and thus inhibits breast cancer proliferation and metastasis both in vitro and in vivo. Our data establish the importance of aberrant FOXA1 O-GlcNAcylation in breast cancer progression and indicate that targeting O-GlcNAcylation is a therapeutic strategy for metastatic breast cancer.
URL[Source Record]
Indexed By
Language
English
Important Publications
NI Journal Papers
SUSTech Authorship
Others
Funding Project
National Natural Science Foundation of China[31971214] ; Fundamental Research Funds for the Central Universities[DUT22YG131]
WOS Research Area
Science & Technology - Other Topics
WOS Subject
Multidisciplinary Sciences
WOS Accession No
WOS:001050899400008
Publisher
Data Source
Web of Science
Citation statistics
Cited Times [WOS]:0
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/553408
DepartmentDepartment of Chemistry
Affiliation
1.Dalian Univ Technol, Sch Life & Pharmaceut Sci, Panjin, Peoples R China
2.Beijing Univ Technol, Fac Environm & Life, Beijing, Peoples R China
3.Beijing Int Sci & Technol Cooperat Base Intelligen, Beijing, Peoples R China
4.Southern Univ Sci & Technol, Coll Sci, Dept Chem, Shenzhen, Peoples R China
5.Univ Hong Kong, Dept Chem, Hong Kong, Peoples R China
6.Lab Synthet Chem & Chem Biol Ltd, Hong Kong Sci Pk,Sci Pk West Ave, Hong Kong, Peoples R China
7.Xuzhou Med Univ, Blood Dis Inst, Xuzhou, Jiangsu, Peoples R China
8.Nanjing Med Univ, Affiliated Huaian Peoples Hosp No 1, Dept Oncol, Huaian, Peoples R China
9.Chinese Acad Sci, Dalian Inst Chem Phys, Lab Mol Modeling & Design, State Key Lab Mol React Dynam, Dalian, Peoples R China
Recommended Citation
GB/T 7714
Liu, Yajie,Yu, Kairan,Kong, Xiaotian,et al. FOXA1 O-GlcNAcylation-mediated transcriptional switch governs metastasis capacity in breast cancer[J]. SCIENCE ADVANCES,2023,9(33).
APA
Liu, Yajie.,Yu, Kairan.,Kong, Xiaotian.,Zhang, Keren.,Wang, Lingyan.,...&Liu, Yubo.(2023).FOXA1 O-GlcNAcylation-mediated transcriptional switch governs metastasis capacity in breast cancer.SCIENCE ADVANCES,9(33).
MLA
Liu, Yajie,et al."FOXA1 O-GlcNAcylation-mediated transcriptional switch governs metastasis capacity in breast cancer".SCIENCE ADVANCES 9.33(2023).
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