Effective anti-aromatase therapy to battle against estrogen-mediated breast cancer: Comparative SAR/QSAR assessment on steroidal aromatase inhibitors

Eur J Med Chem. 2020 Dec 15:208:112845. doi: 10.1016/j.ejmech.2020.112845. Epub 2020 Sep 16.

Abstract

A large number of world women populations are suffering from breast cancer. It is increasing day by day that is quite alarming. The major reason behind breast tumors is upregulation of estrogen which is dependent on aromatase. Aromatase inhibitors (AIs) have opened up a new era to combat the battle against estrogen-mediated breast cancer. Despite several advantages, various adverse effects have limited the use of AIs. Therefore, it is still a demanding and challenging job to design selective AIs with fewer adverse effects. In this article, comparative quantitative structure-activity relationship (QSAR) study of steroidal aromatase inhibitors (SAIs) have been discussed in details to get an insight into the structural and physicochemical properties of SAIs controlling the aromatase inhibitory activity. This study reflects that SAIs should possess smaller shape and size with less bulky substituents having lesser polarity and less steric effect along with greater hydrophobicity for the higher aromatase inhibitory activity. This study will obviously shed light into the newer idea for the medicinal chemists to design and discover novel, effective and less toxic SAIs to combat the life-threatening breast cancer as well as to initiate a modern era in breast cancer drug discovery.

Keywords: Aromatase; Estrogen-mediated breast tumor; Quantitative structure-activity relationship (QSAR); Steroidal aromatase inhibitor; Structure-activity relationship (SAR).

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / therapeutic use*
  • Aromatase / metabolism
  • Aromatase Inhibitors / chemistry
  • Aromatase Inhibitors / metabolism
  • Aromatase Inhibitors / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Estrogens / metabolism*
  • Humans
  • Molecular Docking Simulation
  • Molecular Structure
  • Quantitative Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Aromatase Inhibitors
  • Estrogens
  • Aromatase