14-3-3σ-NEDD4L axis promotes ubiquitination and degradation of HIF-1α in colorectal cancer

Sicheng Liu, Rui Guo, Hui Xu, Jinneng Yang, Haidan Luo, Sai Ching Jim Yeung, Kai Li, Mong Hong Lee, Runxiang Yang

    Research output: Contribution to journalArticlepeer-review

    1 Scopus citations

    Abstract

    A hypoxic microenvironment contributes to tumor progression, with hypoxia-inducible factor-1α (HIF-1α) being a critical regulator. We have reported that 14-3-3σ is negatively associated with HIF-1α expression; however, its role in hypoxia-induced tumor progression remains poorly characterized. Here we show that 14-3-3σ suppresses cancer hypoxia-induced metastasis and angiogenesis in colorectal cancer (CRC). 14-3-3σ opposes HIF-1α expression by regulating the protein stability of HIF-1α, thereby decreasing HIF-1α transcriptional activity and suppressing tumor progression. Mechanistic studies show that the 14-3-3σ-interacting protein neural precursor cell-expressed developmentally down-regulated 4-like (NEDD4L) is an E3 ligase that targets HIF-1α. 14-3-3σ promotes the binding of S448-phosphorylated NEDD4L to HIF-1α, thereby enhancing HIF-1α poly-ubiquitination and subsequent proteasome-mediated degradation. Consistent with this anti-tumorigenic function for 14-3-3σ, low 14-3-3σ expression levels correlate with poor CRC patient survival, and 14-3-3σ enhances the response of CRC to bevacizumab. These results reveal an important mechanism for 14-3-3σ in tumor suppression through HIF-1α regulation.

    Original languageEnglish (US)
    Article number112870
    JournalCell Reports
    Volume42
    Issue number8
    DOIs
    StatePublished - Aug 29 2023

    Keywords

    • 14-3-3σ
    • bevacizumab
    • colorectal cancer
    • CP: Cancer
    • HIF-1α
    • NEDD4L
    • ubiquitination

    ASJC Scopus subject areas

    • General Biochemistry, Genetics and Molecular Biology

    Fingerprint

    Dive into the research topics of '14-3-3σ-NEDD4L axis promotes ubiquitination and degradation of HIF-1α in colorectal cancer'. Together they form a unique fingerprint.

    Cite this