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Givinostat and hydroxyurea synergize in vitro to induce apoptosis of cells from JAK2(V617F) myeloproliferative neoplasm patients.

Abstract
We investigated whether clinically achievable concentrations of the histone deacetylase (HDAC) inhibitors givinostat and hydroxyurea induce synergistic cytotoxicity in Jak2(V617F) cells in vitro and through which possible mechanism. Givinostat and hydroxyurea at low doses potentiated the pro-apoptotic effects of each other in the Jak2(V617F) HEL and UKE1 cell lines. Givinostat induced 6.8%-20.8% and hydroxyurea (HU) 20.4%-42.4% cell death alone and 35.8%-75.3% in combination. The effect was statistically significant using the median effect Chou-Talalay method, resulting in a combination index less than 1, indicating synergy. Givinostat alone induced cell cycle arrest of the cell lines in G0/G1 and hydroxyurea in S phase, whereas both drugs together led to a G1 block. At the molecular level, hydroxyurea counteracted the induction of p21CDKN1A by Givinostat and potentiated caspase 3 activation, explaining at least in part the increased apoptosis observed in presence of both compounds. We also verified the effect of the same drugs in colony assays of freshly isolated Jak2(V617F) polycythemia vera cells. In this case, low doses of the compounds were additive to each other. These results suggest that combined treatment with givinostat and hydroxyurea is a potential strategy for the management of Jak2(V617F) myeloproliferative neoplasms.
AuthorsAriel Amaru Calzada, Olga Pedrini, Guido Finazzi, Flavio Leoni, Paolo Mascagni, Martino Introna, Alessandro Rambaldi, Josée Golay, Associazione Italiana per la Ricerca sul Cancro-Gruppo Italiano Malattie Mieloproliferative Investigators
JournalExperimental hematology (Exp Hematol) Vol. 41 Issue 3 Pg. 253-60.e2 (Mar 2013) ISSN: 1873-2399 [Electronic] Netherlands
PMID23111067 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.
Chemical References
  • Antineoplastic Agents
  • CDKN1A protein, human
  • Carbamates
  • Cyclin-Dependent Kinase Inhibitor p21
  • givinostat
  • Janus Kinase 2
  • Caspase 3
  • Hydroxyurea
Topics
  • Amino Acid Substitution
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • Blotting, Western
  • Carbamates (pharmacology)
  • Caspase 3 (metabolism)
  • Cell Cycle Checkpoints (drug effects)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Cells, Cultured
  • Cyclin-Dependent Kinase Inhibitor p21 (metabolism)
  • Drug Synergism
  • Humans
  • Hydroxyurea (pharmacology)
  • Janus Kinase 2 (genetics, metabolism)
  • Leukocytes, Mononuclear (drug effects, metabolism, pathology)
  • Mutation
  • Myeloproliferative Disorders (blood, genetics, pathology)
  • Polycythemia Vera (blood, metabolism, pathology)

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