p53 destabilizing protein skews asymmetric division and enhances NOTCH activation to direct self-renewal of TICs

Nat Commun. 2020 Jun 17;11(1):3084. doi: 10.1038/s41467-020-16616-8.

Abstract

Tumor-initiating stem-like cells (TICs) are defective in maintaining asymmetric cell division and responsible for tumor recurrence. Cell-fate-determinant molecule NUMB-interacting protein (TBC1D15) is overexpressed and contributes to p53 degradation in TICs. Here we identify TBC1D15-mediated oncogenic mechanisms and tested the tumorigenic roles of TBC1D15 in vivo. We examined hepatocellular carcinoma (HCC) development in alcohol Western diet-fed hepatitis C virus NS5A Tg mice with hepatocyte-specific TBC1D15 deficiency or expression of non-phosphorylatable NUMB mutations. Liver-specific TBC1D15 deficiency or non-p-NUMB expression reduced TIC numbers and HCC development. TBC1D15-NuMA1 association impaired asymmetric division machinery by hijacking NuMA from LGN binding, thereby favoring TIC self-renewal. TBC1D15-NOTCH1 interaction activated and stabilized NOTCH1 which upregulated transcription of NANOG essential for TIC expansion. TBC1D15 activated three novel oncogenic pathways to promote self-renewal, p53 loss, and Nanog transcription in TICs. Thus, this central regulator could serve as a potential therapeutic target for treatment of HCC.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Carcinogenesis / pathology
  • Carcinoma, Hepatocellular / metabolism
  • Cell Division
  • Cell Line, Tumor
  • Fluorescence Resonance Energy Transfer
  • GTPase-Activating Proteins / metabolism*
  • Hepacivirus
  • Hepatocytes / cytology
  • Humans
  • Liver / metabolism
  • Liver Neoplasms / metabolism
  • Mice
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Neoplastic Stem Cells / cytology*
  • Phosphorylation
  • Receptor, Notch1 / metabolism*
  • Receptors, Notch / metabolism
  • Signal Transduction
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • GTPase-Activating Proteins
  • NOTCH1 protein, human
  • Receptor, Notch1
  • Receptors, Notch
  • TBC1D15 protein, human
  • TP53 protein, human
  • Tumor Suppressor Protein p53