The olive oil phenolic (-)-oleocanthal modulates estrogen receptor expression in luminal breast cancer in vitro and in vivo and synergizes with tamoxifen treatment

Eur J Pharmacol. 2017 Sep 5:810:100-111. doi: 10.1016/j.ejphar.2017.06.019. Epub 2017 Jun 15.

Abstract

Luminal breast cancer represents a therapeutic challenge in terms of aggressive disease and emerging resistance to targeted therapy. (-)-Oleocanthal has demonstrated anticancer activity in multiple human cancers. The goal of this study was to explore the effect of (-)-oleocanthal treatment on growth of luminal breast cancer cells and to examine the effect of combination of (-)-oleocanthal with tamoxifen. Results showed that (-)-oleocanthal inhibited growth of BT-474, MCF-7, and T-47D human breast cancer cells in mitogen-free media with IC50 values of 32.7, 24.07, and 80.93µM, respectively. Similarly, (-)-oleocanthal suppressed growth of BT-474, MCF-7, and T-47D cells in 17β-estradiol-supplemented media with IC50 values of 22.28, 20.77, and 83.91µM, respectively. Combined (-)-oleocanthal and tamoxifen treatments resulted in a synergistic growth inhibition of BT-474, MCF-7, and T-47D cells with combination index values of 0.65, 0.61, and 0.53 for each cell line, respectively. In-silico docking studies indicated high degree of overlapping for the binding of (-)-oleocanthal and 17β-estradiol to estrogen receptors, while (-)-oleocanthal and tamoxifen have distinguished binding modes. Treatment with 5mg/kg or 10mg/kg (-)-oleocanthal resulted in 97% inhibition of tumor growth in orthotopic athymic mice bearing BT-474 tumor xenografts compared to vehicle-treated animals. (-)-Oleocanthal treatment reduced total levels of estrogen receptors in BT-474 cells both in vitro and in vivo. Collectively, (-)-oleocanthal showed a potential beneficial effect in suppressing growth of hormone-dependent breast cancer and improving sensitivity to tamoxifen treatment. These findings provide rational for evaluating the effect of (-)-oleocanthal in combination with endocrine treatments in luminal breast cancer.

Keywords: (-)-Oleocanthal; 17β-estradiol; 17β-estradiol (PubChem CID: 5757); Breast cancer; Estrogen receptor; Luminal B; Oleocanthal (PubChem CID: 11652416); Tamoxifen; Tamoxifen (PubChem CID: 2733526).

MeSH terms

  • Aldehydes / metabolism
  • Aldehydes / pharmacology*
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology*
  • Breast Neoplasms / pathology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cyclopentane Monoterpenes
  • Drug Synergism
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Humans
  • Molecular Docking Simulation
  • Olive Oil / chemistry*
  • Phenols / metabolism
  • Phenols / pharmacology*
  • Protein Conformation
  • Receptors, Estrogen / chemistry
  • Receptors, Estrogen / metabolism*
  • Tamoxifen / metabolism
  • Tamoxifen / pharmacology*
  • Xenograft Model Antitumor Assays

Substances

  • Aldehydes
  • Antineoplastic Agents
  • Cyclopentane Monoterpenes
  • Olive Oil
  • Phenols
  • Receptors, Estrogen
  • Tamoxifen
  • oleocanthal