CR-LAAO antileukemic effect against Bcr-Abl(+) cells is mediated by apoptosis and hydrogen peroxide

Int J Biol Macromol. 2016 May:86:309-20. doi: 10.1016/j.ijbiomac.2016.01.069. Epub 2016 Jan 23.

Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm characterized by the presence of the Bcr-Abl tyrosine kinase protein, which confers resistance to apoptosis in leukemic cells. Tyrosine kinase inhibitors (TKIs) are effectively used to treat CML; however, CML patients in the advanced (CML-AP) and chronic (CML-CP) phases of the disease are usually resistant to TKI therapy. Thus, it is necessary to seek for novel agents to treat CML, such as the enzyme l-amino acid oxidase from Calloselasma rhodostoma (CR-LAAO) snake venom. We examined the antitumor effect of CR-LAAO in Bcr-Abl(+) cell lines and peripheral blood mononuclear cells (PBMC) from healthy subjects and CML patients. CR-LAAO was more cytotoxic towards Bcr-Abl(+) cell lines than towards healthy subjects' PBMC. The H2O2 produced during the enzymatic action of CR-LAAO mediated its cytotoxic effect. The CR-LAAO induced apoptosis in Bcr-Abl(+) cells, as detected by caspases 3, 8, and 9 activation, loss of mitochondrial membrane potential, and DNA damage. CR-LAAO elicited apoptosis in PBMC from CML-CP patients without TKI treatment more strongly than in PBMC from healthy subjects and TKI-treated CML-CP and CML-AP patients. The antitumor effect of CR-LAAO against Bcr-Abl(+) cells makes this toxin a promising candidate to CML therapy.

Keywords: Apoptosis; CR-LAAO; Calloselasma rhodostoma; Chronic myeloid leukemia; Tyrosine-kinase inhibitors; l-Amino acid oxidase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Apoptosis / drug effects*
  • Caspases / metabolism
  • Cell Line, Tumor
  • Crotalid Venoms / enzymology*
  • DNA Damage
  • Drug Interactions
  • Enzyme Activation / drug effects
  • Female
  • Fusion Proteins, bcr-abl / metabolism*
  • Humans
  • Hydrogen Peroxide / metabolism*
  • L-Amino Acid Oxidase / pharmacology*
  • L-Amino Acid Oxidase / therapeutic use
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / blood
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / metabolism
  • Leukocytes, Mononuclear / pathology
  • Male
  • Membrane Potential, Mitochondrial / drug effects
  • Middle Aged
  • Protein Kinase Inhibitors / pharmacology
  • Protein-Tyrosine Kinases / antagonists & inhibitors

Substances

  • Antineoplastic Agents
  • Crotalid Venoms
  • Protein Kinase Inhibitors
  • Hydrogen Peroxide
  • L-Amino Acid Oxidase
  • Protein-Tyrosine Kinases
  • Fusion Proteins, bcr-abl
  • Caspases