Murine double minute 2 regulates Hu antigen R stability in human liver and colon cancer through NEDDylation

Hepatology. 2012 Apr;55(4):1237-48. doi: 10.1002/hep.24795. Epub 2012 Mar 1.

Abstract

Hu antigen R (HuR) is a central RNA-binding protein regulating cell dedifferentiation, proliferation, and survival, which are well-established hallmarks of cancer. HuR is frequently overexpressed in tumors correlating with tumor malignancy, which is in line with a role for HuR in tumorigenesis. However, the precise mechanism leading to changes in HuR expression remains unclear. In the liver, HuR plays a crucial role in hepatocyte proliferation, differentiation, and transformation. Here, we unraveled a novel mean of regulation of HuR expression in hepatocellular carcinoma (HCC) and colon cancer. HuR levels correlate with the abundance of the oncogene, murine double minute 2 (Mdm2), in human HCC and colon cancer metastases. HuR is stabilized by Mdm2-mediated NEDDylation in at least three lysine residues, ensuring its nuclear localization and protection from degradation.

Conclusion: This novel Mdm2/NEDD8/HuR regulatory framework is essential for the malignant transformation of tumor cells, which, in turn, unveils a novel signaling paradigm that is pharmacologically amenable for cancer therapy.

Publication types

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

MeSH terms

  • Animals
  • Carcinoma, Hepatocellular / metabolism*
  • Carcinoma, Hepatocellular / pathology
  • Case-Control Studies
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Cell Transformation, Neoplastic / pathology
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Cytoplasm / metabolism
  • Disease Models, Animal
  • ELAV Proteins / metabolism*
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Humans
  • Liver Neoplasms / metabolism*
  • Liver Neoplasms / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NEDD8 Protein
  • Proto-Oncogene Proteins c-mdm2 / metabolism*
  • Signal Transduction / physiology
  • Ubiquitins / metabolism*

Substances

  • ELAV Proteins
  • NEDD8 Protein
  • NEDD8 protein, human
  • Nedd8 protein, mouse
  • Ubiquitins
  • MDM2 protein, human
  • Mdm2 protein, mouse
  • Proto-Oncogene Proteins c-mdm2