The cytotoxicity of Scytosiphon lomentaria against HL-60 promyelocytic leukemia cells

Cancer Biother Radiopharm. 2004 Oct;19(5):641-8. doi: 10.1089/cbr.2004.19.641.

Abstract

This study examined the cytotoxicity of Scytosiphon lomentaria, using various cancer cell lines. The ethyl acetate (EtOAc) fraction of this alga showed the cytotoxicity to leukemia cells, including HL-60. When HL-60 cells were treated with its EtOAc fraction, several apoptotic characteristics, such as DNA fragmentation, chromatin condensation, and an increase of the population of sub-G1 hypodiploid cells, were observed. Moreover, the EtOAc fraction decreased c-Myc expression in a dose-dependent manner. In order to understand the mechanism of apoptosis induction by S. lomentaria, we examined the changes of Bcl-2 and Bax protein expression levels. The EtOAc fraction reduced Bcl-2, an antiapoptotic protein, but increased Bax, a proapoptotic protein, in a dose-dependent manner. When we examined the activation of caspase-3, an effector of apoptosis, the expression of the active form (19 kDa) of caspase-3 increased, and the increase of their activities was demonstrated by the cleavage of poly (ADP-ribose) polymerase, a substrate of caspase-3, to 85 kDa. The results suggest that the inhibitory effect of S. lomentaria on the growth of HL-60 appears to arise from the induction of apoptosis by way of the down-regulation of Bcl-2 and the activation of caspase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / pharmacology*
  • Apoptosis
  • Blotting, Western
  • Caspase 3
  • Caspases / biosynthesis
  • Cell Nucleus / metabolism
  • Chromatin / drug effects
  • DNA / drug effects
  • DNA Fragmentation / drug effects
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Enzyme Activation
  • Enzyme Inhibitors
  • Eukaryota / metabolism*
  • G1 Phase
  • Gene Expression Regulation, Neoplastic
  • HL-60 Cells
  • Humans
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Proto-Oncogene Proteins c-myc / biosynthesis
  • Time Factors
  • bcl-2-Associated X Protein

Substances

  • Acetates
  • BAX protein, human
  • Chromatin
  • Enzyme Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • Proto-Oncogene Proteins c-myc
  • bcl-2-Associated X Protein
  • ethyl acetate
  • DNA
  • CASP3 protein, human
  • Caspase 3
  • Caspases