Autophagy is associated with cucurbitacin D-induced apoptosis in human T cell leukemia cells

Med Oncol. 2016 Apr;33(4):30. doi: 10.1007/s12032-016-0743-y. Epub 2016 Feb 25.

Abstract

We previously reported that the inflammasome inhibitor cucurbitacin D (CuD) induces apoptosis in human leukemia cell lines. In the present study, we investigated the effects of co-treatment with an additional Bcl-xL inhibitor, Z36. Treatment with Z36 induced cell death in leukemia cell lines, with MT-4 cells exhibiting the lowest sensitivity to Z36. Co-treatment of cells with Z36 and CuD resulted in a greater degree of cell death for Hut78 and Jurkat cells than treatment with CuD alone. In contrast, co-treatment of MT-4 cells with Z36 and CuD had a suppressive effect on cell death. The autophagy inhibitor 3-methyladenine (3-MA) suppressed the growth of leukemia cell lines HuT78, Jurkat, MT-1, and MT-4. CuD-induced cell death was enhanced by 3-MA in Jurkat cells, but inhibited in MT-4 cells. Western blotting results revealed cleavage of poly(ADP ribose) polymerase (PARP), supporting CuD-induced cell death; 3-MA enhanced CuD-Z36-induced PARP cleavage. Taken together, our results indicate that autophagy negatively regulates chemical-induced cell death of leukemia cells, and that controlling autophagy could be beneficial in the development of more effective chemotherapies against leukemia.

Keywords: Adult T cell leukemia; Apoptosis; Autophagy; Cucurbitacin D; Z36.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / pharmacology
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology
  • Apoptosis / drug effects
  • Autophagy / drug effects*
  • Beclin-1 / genetics
  • Beclin-1 / metabolism
  • Cell Line, Tumor / drug effects
  • Humans
  • Indoles / administration & dosage
  • Indoles / pharmacology
  • Jurkat Cells / drug effects
  • Leukemia, T-Cell / drug therapy*
  • Leukemia, T-Cell / pathology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Triterpenes / administration & dosage
  • Triterpenes / pharmacology*
  • bcl-X Protein / antagonists & inhibitors

Substances

  • 5-fluoro-1-(3'-dimethylamino)propyl-indolin-2-one
  • BCL2L1 protein, human
  • BECN1 protein, human
  • Beclin-1
  • Indoles
  • Triterpenes
  • bcl-X Protein
  • 3-methyladenine
  • cucurbitacin D
  • Poly(ADP-ribose) Polymerases
  • Adenine