Pharmacotherapeutics and Molecular Mechanism of Phytochemicals in Alleviating Hormone-Responsive Breast Cancer.
Shailima RampoguChanin ParkRavinder DonetiMinky SonAyoung BaekAmir ZebRohit BaviRaj KumarGihwan LeeShraddha ParateSmita C PawarYohan ParkSeok Ju ParkKeun Woo LeePublished in: Oxidative medicine and cellular longevity (2019)
Breast cancer (BC) is the leading cause of death among women worldwide devoid of effective treatment. It is therefore important to develop agents that can reverse, reduce, or slow the growth of BC. The use of natural products as chemopreventive agents provides enormous advantages. The aim of the current investigation is to determine the efficacy of the phytochemicals against BC along with the approved drugs to screen the most desirable and effective phytocompound. In the current study, 36 phytochemicals have been evaluated against aromatase to identify the potential candidate drug along with the approved drugs employing the Cdocker module accessible on the Discovery Studio (DS) v4.5 and thereafter analysing the stability of the protein ligand complex using GROningen MAchine for Chemical Simulations v5.0.6 (GROMACS). Additionally, these compounds were assessed for the inhibitory features employing the structure-based pharmacophore (SBP). The Cdocker protocol available with the DS has computed higher dock scores for the phytochemicals complemented by lower binding energies. The top-ranked compounds that have anchored with key residues located at the binding pocket of the protein were subjected to molecular dynamics (MD) simulations employing GROMACS. The resultant findings reveal the stability of the protein backbone and further guide to comprehend on the involvement of key residues Phe134, Val370, and Met374 that mechanistically inhibit BC. Among 36 compounds, curcumin, capsaicin, rosmarinic acid, and 6-shogaol have emerged as promising phytochemicals conferred with the highest Cdocker interaction energy, key residue interactions, stable MD results than reference drugs, and imbibing the key inhibitory features. Taken together, the current study illuminates the use of natural compounds as potential drugs against BC. Additionally, these compounds could also serve as scaffolds in designing and development of new drugs.
Keyphrases
- molecular dynamics
- density functional theory
- binding protein
- high throughput
- amino acid
- randomized controlled trial
- drug induced
- small molecule
- magnetic resonance
- emergency department
- computed tomography
- metabolic syndrome
- type diabetes
- human health
- magnetic resonance imaging
- adipose tissue
- gene expression
- machine learning
- molecular dynamics simulations
- polycystic ovary syndrome
- tyrosine kinase
- molecular docking
- risk assessment
- cancer therapy
- young adults
- pregnancy outcomes
- adverse drug
- tissue engineering