The ubiquitin-activating enzyme E1 as a therapeutic target for the treatment of leukemia and multiple myeloma

Blood. 2010 Mar 18;115(11):2251-9. doi: 10.1182/blood-2009-07-231191. Epub 2010 Jan 14.

Abstract

The proteasomal pathway of protein degradation involves 2 discrete steps: ubiquitination and degradation. Here, we evaluated the effects of inhibiting the ubiquitination pathway at the level of the ubiquitin-activating enzyme UBA1 (E1). By immunoblotting, leukemia cell lines and primary patient samples had increased protein ubiquitination. Therefore, we examined the effects of genetic and chemical inhibition of the E1 enzyme. Knockdown of E1 decreased the abundance of ubiquitinated proteins in leukemia and myeloma cells and induced cell death. To further investigate effects of E1 inhibition in malignancy, we discovered a novel small molecule inhibitor, 3,5-dioxopyrazolidine compound, 1-(3-chloro-4-fluorophenyl)-4-[(5-nitro-2-furyl)methylene]-3,5-pyrazolidinedione (PYZD-4409). PYZD-4409 induced cell death in malignant cells and preferentially inhibited the clonogenic growth of primary acute myeloid leukemia cells compared with normal hematopoietic cells. Mechanistically, genetic or chemical inhibition of E1 increased expression of E1 stress markers. Moreover, BI-1 overexpression blocked cell death after E1 inhibition, suggesting ER stress is functionally important for cell death after E1 inhibition. Finally, in a mouse model of leukemia, intraperitoneal administration of PYZD-4409 decreased tumor weight and volume compared with control without untoward toxicity. Thus, our work highlights the E1 enzyme as a novel target for the treatment of hematologic malignancies.

Publication types

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

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cyclin D3 / metabolism
  • Disease Models, Animal
  • Drug Screening Assays, Antitumor
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / pathology
  • Enzyme Inhibitors / pharmacology
  • Gene Knockdown Techniques
  • Hematopoietic System / cytology
  • Hematopoietic System / drug effects
  • Humans
  • Leukemia / enzymology*
  • Leukemia / therapy*
  • Mice
  • Multiple Myeloma / enzymology*
  • Multiple Myeloma / therapy*
  • Protein Processing, Post-Translational / drug effects
  • Small Molecule Libraries / pharmacology
  • Stress, Physiological / drug effects
  • Time Factors
  • Tumor Suppressor Protein p53 / metabolism
  • Ubiquitin-Activating Enzymes / antagonists & inhibitors
  • Ubiquitin-Activating Enzymes / metabolism*
  • Ubiquitination / drug effects

Substances

  • Cyclin D3
  • Enzyme Inhibitors
  • Small Molecule Libraries
  • Tumor Suppressor Protein p53
  • Ubiquitin-Activating Enzymes