Cytotoxic activity of octahydropyrazin[2,1-a:5,4-a']diisoquinoline derivatives in human breast cancer cells

Arch Pharm Res. 2015;38(5):628-41. doi: 10.1007/s12272-014-0444-z. Epub 2014 Jul 25.

Abstract

Evaluation of the cytotoxicity of novel octahydropyrazin[2,1-a:5,4-a']diisoquinoline derivatives (1a-2c) employing a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and inhibition of [(3)H]thymidine incorporation into DNA demonstrated that these compounds were more active than etoposide and camptothecin in both MDA-MB-231 and MCF-7 human breast cancer cells. Flow cytometric analysis after Annexin V-FITC and propidium iodide staining also confirmed that apoptosis was the main response of human breast cancer cells to 1a-2c treatment. Our results suggest that apoptosis of human breast cancer cells in the presence of 1a-2c follows the mitochondrial pathway, with the decrease in mitochondrial membrane potential and activation of caspase 9, as well as by the external pathway with the significant increase in caspase 8 expression. Cytotoxic properties of compounds 1a-2c in cultured human breast cancer cells correlate to their ability to inhibit topoisomerase I/II.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / toxicity*
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Breast Neoplasms / metabolism*
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cytotoxins / chemistry
  • Cytotoxins / toxicity*
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Isoquinolines / chemistry
  • Isoquinolines / toxicity*
  • MCF-7 Cells
  • Membrane Potential, Mitochondrial / drug effects
  • Membrane Potential, Mitochondrial / physiology
  • Pyrazines / chemistry
  • Pyrazines / toxicity*

Substances

  • Antineoplastic Agents
  • Cytotoxins
  • Isoquinolines
  • Pyrazines
  • isoquinoline