XIAP inhibits autophagy via XIAP-Mdm2-p53 signalling

EMBO J. 2013 Aug 14;32(16):2204-16. doi: 10.1038/emboj.2013.133. Epub 2013 Jun 7.

Abstract

The primary role of autophagy is adaption to starvation. However, increasing evidence suggests that autophagy inhibition also plays an important role in tumorigenesis. Upregulation of X-linked inhibitor of apoptosis (XIAP) has been associated to a variety of human cancers, yet the underlying mechanisms remain obscure. Here, we report that XIAP suppresses autophagy by exerting a previously unidentified ubiquitin E3 ligase activity towards Mdm2, which is a negative regulator of p53. XIAP controls serum starvation-induced autophagy downstream of the PI3K/Akt pathway. In mouse models, inhibition of autophagy by XIAP promotes tumorigenecity of HCT116 cells. XIAP-mediated autophagy inhibition is also largely validated in clinical tumour samples. These findings reveal a novel XIAP-Mdm2-p53 pathway that mediates the inhibition of autophagy, by which XIAP may contribute to tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / physiology*
  • Blotting, Western
  • Cell Transformation, Neoplastic / metabolism*
  • HCT116 Cells
  • HEK293 Cells
  • Humans
  • Immunohistochemistry
  • Immunoprecipitation
  • Mice
  • Microscopy, Electron
  • Proto-Oncogene Proteins c-mdm2 / metabolism*
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Signal Transduction / physiology*
  • Starvation / physiopathology
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53 / metabolism*
  • Ubiquitin-Protein Ligases / metabolism*
  • X-Linked Inhibitor of Apoptosis Protein / metabolism*

Substances

  • RNA, Small Interfering
  • Tumor Suppressor Protein p53
  • X-Linked Inhibitor of Apoptosis Protein
  • Proto-Oncogene Proteins c-mdm2
  • Ubiquitin-Protein Ligases