Vincristine activates c-Jun N-terminal kinase in chronic lymphocytic leukaemia in vivo

Br J Clin Pharmacol. 2015 Sep;80(3):493-501. doi: 10.1111/bcp.12624. Epub 2015 May 19.

Abstract

Aims: The authors' aim was to conduct a proof-of-principle study to test whether c-Jun N-terminal kinase (JNK) phosphorylation and Noxa induction occur in peripheral blood chronic lymphocytic leukaemia (CLL) cells in patients receiving a vincristine infusion.

Methods: Patients with CLL received 2 mg vincristine by a 5-min intravenous infusion. Blood samples were collected at baseline and up to 6 h after the vincristine infusion, and assayed for JNK activation, Noxa induction and vincristine plasma concentrations.

Results: Ex vivo treated peripheral CLL cells activated JNK in response to 10-100 nM vincristine in 6 h. Noxa protein expression, while variable, was also observed over this time frame. In CLL patients, vincristine infusion led to rapid (<1 h) JNK phosphorylation in peripheral blood CLL cells which was sustained for at least 4-6 h after the vincristine infusion. Noxa protein expression was not observed in response to vincristine infusion.

Conclusions: This study confirmed that vincristine can activate JNK but not induce Noxa in CLL cells in vivo. The results suggest that novel JNK-dependent drug combinations with vincristine warrant further investigation.

Keywords: Noxa; apoptosis; c-Jun N-terminal kinase; chronic lymphocytic leukaemia; vincristine.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antineoplastic Agents, Phytogenic / administration & dosage
  • Antineoplastic Agents, Phytogenic / pharmacokinetics
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Enzyme Activation / drug effects
  • Humans
  • Infusions, Intravenous
  • JNK Mitogen-Activated Protein Kinases / blood
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Leukemia, Lymphocytic, Chronic, B-Cell / blood
  • Leukemia, Lymphocytic, Chronic, B-Cell / enzymology*
  • Lymphocytes / drug effects
  • Lymphocytes / enzymology
  • Phosphorylation
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Vincristine / administration & dosage
  • Vincristine / pharmacokinetics
  • Vincristine / pharmacology*

Substances

  • Antineoplastic Agents, Phytogenic
  • PMAIP1 protein, human
  • Proto-Oncogene Proteins c-bcl-2
  • Vincristine
  • JNK Mitogen-Activated Protein Kinases