Vinblastine rapidly induces NOXA and acutely sensitizes primary chronic lymphocytic leukemia cells to ABT-737

Darcy J P Bates, Alexey Danilov, Christopher H. Lowrey, Alan Eastman

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Proteins of the BCL2 family provide a survival mechanism in many human malignancies, including chronic lymphocytic leukemia (CLL). The BCL2 inhibitor ABT-263 (navitoclax) is active in clinical trials for lymphoid malignancies, yet resistance is expected on the basis of preclinical models.Werecently showed that vinblastine can dramatically sensitize several leukemia cell lines to ABT-737 (the experimental congener of ABT-263). The goal of these experiments was to determine the impact of vinblastine on ABT-737 sensitivity in CLL cells isolated from peripheral blood and to define the underlying mechanism. Freshly isolated CLL cells from 35 patients, as well as normal lymphocytes and platelets, were incubated with various microtubule-disrupting agents plus ABT-737 to assess sensitivity to the single agents and the combination. ABT-737 and vinblastine displayed a range of sensitivity as single agents, and vinblastine markedly sensitized all CLL samples to ABT- 737 within six hours. Vinblastine potently induced the proapoptotic protein PMAIP1 (NOXA) in both time- and dose-dependent manner and this was required for the observed apoptosis. Combretastatin A4, which dissociates microtubules by binding to a different site, had the same effect, confirming that interaction of these agents with microtubules is the initial target. Similarly, vincristine and vinorelbine induced NOXA and enhanced CLL sensitivity to ABT-737. Furthermore, vinblastine plus ABT-737 overcame stroma-mediated resistance to ABT-737 alone. Apoptosis was induced with clinically achievable concentrations with no additional toxicity to normal lymphocytes or platelets. These results suggest that vinca alkaloids may improve the clinical efficacy of ABT-263 in patients with CLL. Mol Cancer Ther; 12(8); 1504-14.

Original languageEnglish (US)
Pages (from-to)1504-1514
Number of pages11
JournalMolecular Cancer Therapeutics
Volume12
Issue number8
DOIs
StatePublished - Aug 2013
Externally publishedYes

Fingerprint

Vinblastine
B-Cell Chronic Lymphocytic Leukemia
Microtubules
Proto-Oncogene Proteins c-bcl-2
Blood Platelets
Lymphocytes
Vinca Alkaloids
Apoptosis
Neoplasms
ABT-737
Vincristine
Leukemia
Clinical Trials
Cell Line
Survival
navitoclax

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Vinblastine rapidly induces NOXA and acutely sensitizes primary chronic lymphocytic leukemia cells to ABT-737. / Bates, Darcy J P; Danilov, Alexey; Lowrey, Christopher H.; Eastman, Alan.

In: Molecular Cancer Therapeutics, Vol. 12, No. 8, 08.2013, p. 1504-1514.

Research output: Contribution to journalArticle

Bates, Darcy J P ; Danilov, Alexey ; Lowrey, Christopher H. ; Eastman, Alan. / Vinblastine rapidly induces NOXA and acutely sensitizes primary chronic lymphocytic leukemia cells to ABT-737. In: Molecular Cancer Therapeutics. 2013 ; Vol. 12, No. 8. pp. 1504-1514.
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