Regulation mechanism of Fbxw7-related signaling pathways (Review)

Oncol Rep. 2015 Nov;34(5):2215-24. doi: 10.3892/or.2015.4227. Epub 2015 Aug 26.

Abstract

F-box and WD repeat domain-containing 7 (Fbxw7), the substrate-recognition component of SCFFbxw7 complex, is thought to be a tumor suppressor involved in cell growth, proliferation, differentiation and survival. Although an increasing number of ubiquitin substrates of Fbxw7 have been identified, the best characterized substrates are cyclin E and c-Myc. Fbxw7/cyclin E and Fbxw7/c-Myc pathways are tightly regulated by multiple regulators. Fbxw7 has been identified as a tumor suppressor in hepatocellular carcinoma. This review focused on the regulation of Fbxw7/cyclin E and Fbxw7/c-Myc pathways and discussed findings to gain a better understanding of the role of Fbxw7 in hepatocellular carcinoma.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Carcinoma, Hepatocellular / enzymology
  • Cell Cycle Proteins / metabolism*
  • Cyclin E / metabolism
  • F-Box Proteins / metabolism*
  • F-Box-WD Repeat-Containing Protein 7
  • Feedback, Physiological
  • Humans
  • Liver Neoplasms / enzymology
  • Proto-Oncogene Proteins c-myc / metabolism
  • Signal Transduction*
  • Ubiquitin-Protein Ligases / metabolism*

Substances

  • Cell Cycle Proteins
  • Cyclin E
  • F-Box Proteins
  • F-Box-WD Repeat-Containing Protein 7
  • FBXW7 protein, human
  • MYC protein, human
  • Proto-Oncogene Proteins c-myc
  • Ubiquitin-Protein Ligases