Breast cancer organoid model allowed to reveal potentially beneficial combinations of 3,3'-diindolylmethane and chemotherapy drugs

Biochimie. 2020 Dec:179:217-227. doi: 10.1016/j.biochi.2020.10.007. Epub 2020 Oct 22.

Abstract

Epigenetic alterations represent promising therapeutic targets in cancer treatment. Recently it was revealed that small molecules have the potential to act as microRNA silencers. Capacity to bind the discrete stem-looped structure of pre-miR-21 and prevent its maturation opens opportunities to utilize such compounds for the prevention of initiation, progression, and chemoresistance of cancer. Molecular simulations performed earlier identified 3,3'-diindolylmethane (DIM) as a potent microRNA-21 antagonist. However, data on DIM and microRNA-21 interplay is controversial, which may be caused by the limitations of the cell lines.

MeSH terms

  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Cyclophosphamide / pharmacology
  • Female
  • Humans
  • Indoles / pharmacology*
  • Methotrexate / pharmacology
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / metabolism
  • Organoids / drug effects*
  • Organoids / metabolism*
  • Organoids / pathology
  • Primary Cell Culture

Substances

  • Indoles
  • MIRN21 microRNA, human
  • MicroRNAs
  • Cyclophosphamide
  • 3,3'-diindolylmethane
  • Methotrexate