Ubiquitin-mediated proteasomal degradation in normal and malignant hematopoiesis

Blood Cells Mol Dis. 2008 Mar-Apr;40(2):200-10. doi: 10.1016/j.bcmd.2007.07.011. Epub 2007 Oct 4.

Abstract

Understanding the molecular mechanisms controlling normal hematopoietic differentiation is critical to develop new treatments for blood diseases and to manipulate stem cells. Despite the identification of many players in hematopoiesis, the molecular mechanisms controlling hematopoietic differentiation remain poorly understood. Due to a number of recent findings, the targeting of regulators of hematopoiesis to proteasomal degradation might be an important step in control of this developmental program.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Hematologic Neoplasms / metabolism*
  • Hematopoiesis*
  • Hematopoietic System / metabolism*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Proteasome Endopeptidase Complex / metabolism*
  • Proteins / metabolism
  • RING Finger Domains / physiology
  • Tumor Suppressor Proteins / metabolism
  • Ubiquitin / metabolism*
  • Ubiquitin-Protein Ligase Complexes / metabolism
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Intracellular Signaling Peptides and Proteins
  • Proteins
  • SOSTDC1 protein, human
  • Tumor Suppressor Proteins
  • Ubiquitin
  • Ubiquitin-Protein Ligase Complexes
  • UBE4B protein, human
  • Ubiquitin-Protein Ligases
  • Proteasome Endopeptidase Complex