In vitro and in vivo effects of xanthorrhizol on human breast cancer MCF-7 cells treated with tamoxifen

J Pharmacol Sci. 2014;125(4):375-85. doi: 10.1254/jphs.14024fp.

Abstract

This study investigated the herb-drug interaction of xanthorrhizol and tamoxifen in human breast cancer cells. Using MCF-7 cell line as an in vitro model, the herb-drug interaction between xanthorrhizol and tamoxifen was measured by MTT assay, luciferase reporter assay, and cell cycle analysis. The effects of xanthorrhizol on growth/autophagy related signaling were determined by immunostaining, western blotting, and real time RT-PCR. Additionally, the in vivo effect of xanthorrhizol and tamoxifen on athymic nude mice implanted with MCF-7 cells was evaluated. When MCF-7 cells were co-treated with tamoxifen and xanthorrhizol, there were no significant changes in terms of cell number, luciferase activity, percentage S-phase cells and LC3-II expression. However, using the MCF-7 implanted nude mice model, it was possible to detect significantly increased tumor volumes, a larger tumor size, and increased protein expression of P38 and P27(Kip1) in the xanthorrhizol + tamoxifen group compared to the tamoxifen-alone group. It can be concluded that while there is no significant herb-drug interaction between xanthorrhizol and tamoxifen in vitro, there is such an interaction in tumor-bearing mice, which provides important information that affects breast cancer treatment translational research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology*
  • Cell Transformation, Neoplastic / drug effects*
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism
  • Disease Models, Animal
  • Drug Therapy, Combination
  • Female
  • Herb-Drug Interactions
  • Humans
  • Luciferases / metabolism
  • MCF-7 Cells
  • Mice, Inbred BALB C
  • Mice, Nude
  • Microtubule-Associated Proteins / metabolism
  • Neoplasm Transplantation
  • Phenols / administration & dosage*
  • Phenols / adverse effects*
  • Phenols / pharmacology
  • Tamoxifen / administration & dosage*
  • Tamoxifen / adverse effects*
  • Tamoxifen / pharmacology

Substances

  • Cdkn1b protein, mouse
  • MAP1LC3A protein, human
  • Microtubule-Associated Proteins
  • Phenols
  • xanthorrhizol
  • Tamoxifen
  • Cyclin-Dependent Kinase Inhibitor p27
  • Luciferases