[10]-Gingerol Reverts Malignant Phenotype of Breast Cancer Cells in 3D Culture

J Cell Biochem. 2017 Sep;118(9):2693-2699. doi: 10.1002/jcb.25906. Epub 2017 May 15.

Abstract

Breast cancer is a complex and multifactorial disease. Tumors have a heterogeneous microenvironment, which have multiple interactions with other cell types, greatly influencing the behavior of tumor cells and response to therapy. The 3D culture mimics the microenvironment better found in vivo and is more appropriated than the traditional 2D culture made from plastic to test the cellular response to drugs. To investigate the effects of [10]-gingerol on breast tumor cells, we used physiologically relevant three-dimensional (3D) cultures of malignant and non-malignant human breast cells grown in laminin-rich extracellular matrix gels (lr-ECM). Our results showed selective cytotoxicity of [10]-gingerol against the malignant T4-2 breast cancer cell line compared to non-malignant S1 cells. The compound reverted the malignant phenotype of the cancer cells, downregulating the expression of epidermal growth factor receptor (EGFR) and β1-integrin. Moreover, [10]-gingerol induced apoptosis in this cell line. These results suggest that [10]-gingerol may be an effective compound to use as adjuvant therapy in breast cancer treatment. J. Cell. Biochem. 118: 2693-2699, 2017. © 2017 Wiley Periodicals, Inc.

Keywords: 3D CULTURE; BREAST CANCER; LAMININ-RICH EXTRACELLULAR MATRIX; MICROENVIRONMENT; NATURAL PRODUCTS; [10]-GINGEROL.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Down-Regulation / drug effects
  • ErbB Receptors / biosynthesis
  • Fatty Alcohols / pharmacology*
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • Guaiacol / analogs & derivatives*
  • Guaiacol / pharmacology
  • Humans
  • Integrin beta1 / biosynthesis
  • Mice, Nude
  • Neoplasm Proteins / biosynthesis

Substances

  • (10)-gingerdiol
  • Fatty Alcohols
  • Integrin beta1
  • Neoplasm Proteins
  • Guaiacol
  • EGFR protein, human
  • ErbB Receptors